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1.
Boston Reentry Study, Massachusetts, 2012-2014 (ICPSR 39307)
Western, Bruce; Braga, Anthony A.; Kohl, Rhiana
Western, Bruce; Braga, Anthony A.; Kohl, Rhiana
The Boston Reentry Study (BRS) was a mixed-methods, longitudinal study of 122 men and women released from Massachusetts state prisons to the Boston area, that focused on the transition into the community during participants' first year after prison release. The original data collection combined a panel survey, qualitative interviews, interviews with family members, and administrative records on criminal history. The BRS examined the complexity of integration after incarceration drawing from participants' life histories, including childhood experiences, to understand how individual biographies shape the transition into the community. This collection includes responses to 5 survey waves: (1) baseline, about one week before release from prison, (2) 1 week after prison release, (3) 2 months after prison release, (4) 6 months after prison release, and (5) 12 months after prison release. The survey collected information on housing, employment, income, health, family relationships, and criminal justice system contact.
2025-03-31
2.
Childhood Adversity and Traumatic Stress among Inpatients at a Psychiatric Hospital in the Baltimore Area from 1993-1995 (ICPSR 36168)
Carlson, Eve
Carlson, Eve
Childhood Adversity and Traumatic Stress among Inpatients at a Psychiatric Hospital in the Baltimore Area from 1993-1995 includes data collected from adult patients at a psychiatric hospital about their experiences and symptoms throughout their lives.
The study sought to address the following research topics:
The capacity of childhood family environment (caretaker dysfunction, neglect, perceived social support), violent abuse (physical and sexual), and individual variables (other abuse) to predict adult psychiatric symptoms of post-traumatic stress disorder, dissociation, and depression.
How psychiatric inpatient research participants appraised the level of upset and potential usefulness of research participation related to trauma-focused research interviews.
What patterns of gaps in memory are reported across types of abuse (physical, sexual, neglect) and other types of traumatic stress.
Whether and how low positive affect is related to specific childhood adversities, including abuse, neglect, caretaker dysfunction, and low childhood social support.
In addition, data from the study were used to develop and validate a self-report measure of traumatic stress symptoms and a brief, structured interview of self-destructiveness.
The data include diagnoses, psychological symptoms, and structured interview responses related to physical and sexual abuse, post-traumatic stress disorder, and self-destructive behavior. Age, sex, marital status, race, and socioeconomic status comprise the demographic data.
2016-04-15
3.
The Common Cold Project: 5 Studies of Behavior, Biology, and the Common Cold (ICPSR 36365)
Cohen, Sheldon
Cohen, Sheldon
The Common Cold Project began in 2011 with the aim of creating, documenting, and archiving a database that combines final research data from 5 prospective viral-challenge studies that were conducted over the preceding 25 years. The data collection includes the British Cold Study (BCS), which focused on psychological stress; the Pittsburgh Cold Study 1 (PCS1), which built on the BCS; the Pittsburgh Cold Study 2 (PCS2), which examined childhood socioeconomic status and personality; the Pittsburgh Mind-Body Center Cold Study (PMBC), which recorded detailed mood and behavior data over 14 days; the Pittsburgh Cold Study 3, which focused on childhood environment; the Pittsburg Cold Study 3 Social Rhythm Data (PCS3-SRM), which recorded daily interview data of mood, health behavior, and social interaction; and finally the 5 Study Aggregate, which was designed to facilitate analysis across studies. These studies assessed predictor (and hypothesized mediating) variables in healthy adults aged 18 to 55 years, experimentally exposed them to a virus that causes the common cold, and then monitored them for development of infection and signs and symptoms of illness. Standard control variables (covariates) included age, sex, socioeconomic status (SES), race/ethnicity, body mass index (BMI), season of the year, and specific antibody (Ab) titer to the challenge virus (specific immunity). Three of the studies also include daily evening interviews (conducted for 6 or 14 days before exposure to a virus and assessing daily social interactions, mood, health behaviors, and physical symptoms; and daily diaries collected during the quarantine period (1 day before and 5-6 days after viral exposure), including cold-specific and nonspecific symptoms, mood, and health behaviors. These data accompany datasets four, five, and seven.
Many common variables were collected across 2 or more studies, and all 5 studies include measures of upper respiratory infectious illness (URI) (e.g., infection, signs and symptoms of a cold, local [nasal mucosa] release of pro- and anti-inflammatory cytokines). Data were also collected on a broad assortment of health-related outcomes not specific to URI including anthropomorphic measures (such as body mass index and waist circumference), complete blood cell counts and differentials, measures of functional immunity, self-reported and objectively assessed health behaviors (smoking, alcohol consumption, physical activity, diet, and sleep), measures of functional physiology across several biological systems (such as pulmonary function, resting cardiovascular function, endocrine, and metabolic activity), and self-reported assessments of physical and psychological health and well-being. In addition, the 5 studies collected data on an extensive range of demographic, health behavior, psychological and social variables including adult SES and subjective social standing, childhood SES, major stressful life events and perceived stress, personality, psychological expectations and beliefs, social relationships, and state and trait affect.
2016-09-02
4.
CRELES-2: Costa Rican Longevity and Healthy Aging Study - Wave 2, 2006-2008 (Costa Rica Estudio de Longevidad y Envejecimiento Saludable, Ronda 2) (ICPSR 31263)
Rosero-Bixby, Luis; Fernández, Xinia; Dow, William H.
Rosero-Bixby, Luis; Fernández, Xinia; Dow, William H.
The Costa Rican Longevity and Healthy Aging Study (CRELES, or Costa Rica Estudio de Longevidad y Envejecimiento Saludable) is a nationally representative longitudinal survey of health and lifecourse experiences of 2,827 Costa Ricans ages 60 and over in 2005, the baseline collection. CRELES-2 refers to the second wave of visits in this longitudinal study, and includes the results from these visits. The first wave of interviews, or baseline, of CRELES is also available at http://doi.org/10.3886/ICPSR26681. The second wave fieldwork was conducted from October 2006 to July 2008, with 2,364 surviving and contacted participants. The original sample was drawn from Costa Rican residents in the 2000 population census who were born in 1945 or before, with an over-sample of the oldest-old (ages 95 and over). Vital statistics indicate that Costa Rica has an unusually high life expectancy for a middle-income country, even higher than that of the United States, but CRELES is the first nationally representative survey to investigate adult health levels in Costa Rica. CRELES public use data files contain information on a broad range of topics including self-reported physical health, psychological health, living conditions, health behaviors, health care utilization, social support, and socioeconomic status. Objective health indicators include anthropometrics, observed mobility, and biomarkers from fasting blood samples (such as cholesterol, glycosylated hemoglobin, and C-reactive protein). Mortality events are tracked and conditions surrounding death are measured in a surviving family interview.
2013-10-23
5.
CRELES-3: Costa Rican Longevity and Healthy Aging Study - Wave 3, 2009 (Costa Rica Estudio de Longevidad y Envejecimiento Saludable, Ronda 3) (ICPSR 35250)
Rosero-Bixby, Luis; Brenes-Camacho, Gilbert; Dow, William H.
Rosero-Bixby, Luis; Brenes-Camacho, Gilbert; Dow, William H.
The Costa Rican Longevity and Healthy Aging Study (CRELES, or Costa Rica Estudio de Longevidad y Envejecimiento Saludable) is a nationally representative longitudinal survey of health and lifecourse experiences. CRELES-3 refers to the third wave of visits in this longitudinal study. The first two waves are available as ICPSR 26681 and ICPSR 31263. The original sample (Wave 1) was drawn from Costa Rican residents in the 2000 population census who were born in 1945 or before, with an over-sample of the oldest age range (ages 95 and over). A total of 2,827 Costa Ricans ages 60 and over participated in 2005. The second wave revisited the same participant group.
The data presented here represent the third wave of fieldwork that was conducted from February 2009 to January 2010, with 1,855 surviving and contacted participants. CRELES data include factors contributing to older adults' length and quality of life. Among these data are self-reported physical health, psychological health, living conditions, health behaviors, health care utilization, social support, and socioeconomic status. Objective health indicators typically included in this series are anthropometrics, observed mobility, and biomarkers from fasting blood (such as cholesterol,
glycosylated hemoglobin, and C-reactive protein). However, the third wave did not collect blood. Data regarding participants' deaths and conditions surrounding death were collected from interviews of surviving family members and are included in Wave 2 and Wave 3 data files. The collection includes a tracking file (Dataset 13) which links participants across the three waves and includes sampling weights. Demographic data included in the study include age during each wave, sex, marital status, education, number of children, type of housing, and geographic region in Costa Rica. Some elements of the demographic data are found only in Wave 1 and require linking the CRELES-3 data files with ICPSR 26681.
2025-04-29
6.
CTDA 1022: Posttraumatic Stress in Children Age 7 to 17 Seen in Hospital for Acute Injury, Australia, 2004-2006 (ICPSR 39196)
Nixon, Reginald D. V.
Nixon, Reginald D. V.
The broad aims of this overall project were to examine predictors of
children's adjustment, mainly post-traumatic stress disorder (PTSD), after a single-incident injury. The overarching hypothesis was that a combination of physiological/biological, cognitive, and parental anxiety factors would predict children's later adjustment. The dataset in this collection comes from the combination of two broad projects that recruited from the same hospitals, with the first (smaller) project being built upon by the second project (which contained additional measures and an additional follow-up).
Children and adolescents aged 7 to 17 and their families (n=135) were recruited for the study after presentation to either of two major metropolitan Australian hospitals following a single-incident injury. Children's heart rate was recorded at hospital triage. Children and parents completed risk screening measures within 4 weeks of injury. Measures for cognitive appraisals, social support, traumatic stress, depression, and anxiety symptoms were assessed at 3 months and 6 months post-injury.
2024-09-18
7.
Development and Implementation of a Digital Ecosystem to Improve Opioid Overdose Reporting, Tracking, and Prevention across Texas, 2020 (ICPSR 38495)
Claborn, Kasey
Claborn, Kasey
This study includes 19 interview transcripts. The overall intent of the interviews was to gather information that could be used to develop and improve a single reporting website for overdose tracking and naloxone distribution metrics that would generate monthly reports to the State of Texas. The goal of this study was to develop and implement a digital ecosystem to improve opioid overdose reporting, tracking, and prevention across Texas. The study also aimed to understand the relationship between substance use behavior, stress response, and social support structures during the COVID-19 pandemic.
2023-01-26
8.
East Asian Social Survey (EASS), Cross-National Survey Data Sets: Network Social Capital in East Asia, 2012 (ICPSR 36277)
Li, Lulu; Kim, Sang-Wook; Iwai, Noriko; Fu, Yang-Chih
Li, Lulu; Kim, Sang-Wook; Iwai, Noriko; Fu, Yang-Chih
The East Asian Social Survey (EASS) is a biennial social survey project that serves as a cross-national network of the following four General Social Survey type surveys in East Asia: the Chinese General Social Survey (CGSS), the Japanese General Social Survey (JGSS), the Korean General Social Survey (KGSS), and the Taiwan Social Change Survey (TSCS), and comparatively examines diverse aspects of social life in these regions. Since its 1st module survey in 2006, EASS produces and disseminates its module survey datasets and this is the harmonized data for the 4th module survey, called 'Network Social Capital in East Asia,' which was carried out in 2012 in the four countries.
Survey information in this module focuses on social networks and participation and attitudes toward various social organizations and events. Respondents were asked about common social interactions, family structures and relationships, their neighborhood environments, social support systems, and their trust toward a range of community members and institutions. Additionally, respondents were asked for their opinions on political issues, and about their participation and experience with voting in recent elections.
Demographic and other background information includes age, sex, marital status, religion, years of education completed, employment status, income, and household size and composition.
2021-10-07
9.
Evaluation of the Linking Systems of Care for Children and Youth Demonstration Project, Illinois, Montana, Ohio, and Virginia, 2015-2019 (ICPSR 37310)
Haas, Stephen; Spooner, Mary Helen
Haas, Stephen; Spooner, Mary Helen
The victimization of children and youth remains a nationwide concern with between 44 percent and 60 percent of children reporting experiences of victimization in national studies. The impacts of victimization, if left unaddressed, can have serious long-term effects on the physical and mental health of children, which vary based on the children's developmental stage and frequency of exposure. The high rates of victimization, coupled with the serious negative consequences of the victimization, underscore the importance of ensuring effective service delivery to meet the needs of this population. Building on decades of work in social change in organizations and communities, the Office for Victims of Crime (OVC), under the United States Department of Justice Strategic Initiative, sought to address the needs of victims of crime. As part of the Strategic Initiative, OVC created the Linking Systems of Care (LSC) for Children and Youth State Demonstration Project, a project intended to directly impact the field of child victimization by bringing together all of the relevant systems and professionals to provide early identification, intervention, and treatment for child and youth victims and their families and caregivers.
2023-05-30
10.
Exposure to Violence, Trauma, and Juvenile Court Involvement: A Longitudinal Analysis of Mobile Youth and Poverty Study Data, Mobile, Alabama, 1998-2011 (ICPSR 37495)
Bolland, Anneliese; Bolland, John M.
Bolland, Anneliese; Bolland, John M.
This project consists of secondary analysis material (syntax only, no data). The original study that the material pertains to is an examination of predominantly African American adolescents who live in extreme poverty. The study suggested that exposure to violence is positively related to involvement in the juvenile court system, and partially mediated by psychological factors, particularly hopelessness; thus, practitioners should take care to target more than just traumatic stress as a result of exposure to violence in African American impoverished youth.
2020-11-24
11.
The Filipino American Community Epidemiological Study (FACES) is a research project of Asian American Recovery Services, Inc. of San Francisco, California. The four-year study, whose formal title is Alcohol-Related Problems among Filipino Americans, was concluded in 1999. It provides information and data about the health of Filipino Americans of the San Francisco Bay Area and the City and County of Honolulu. The interview asked randomly chosen Filipino American respondents in these two geographic areas about their health, alcohol consumption, mood state, physical symptoms, cultural background and sociodemographic information. The purpose of FACES was to study alcohol and stress-related behaviors of Filipino Americans. Demographic variables include gender, age, race, education level, marital status, household income, military service, and religious preference.
2011-08-08
12.
HERO Registry: Creating and Using a Community Registry to Understand the Experiences of Healthcare Workers and Their Communities during COVID-19, United States, 2020-2022 (ICPSR 39153)
O'Brien, Emily; Hernandez, Adrian F.
O'Brien, Emily; Hernandez, Adrian F.
To study the impact of COVID-19 pandemic on frontline healthcare workers in the United States over time, the Healthcare Worker Exposure Response and Outcomes (HERO) Registry was created in 2020 to form a virtual research community of healthcare workers (and later, their family members and community members). The registry was intended for healthcare workers interested in completing research studies related to the COVID-19 pandemic and its impacts on their lives. Observational data were collected at various timepoints between April 2020 and September 2022 via web-based questionnaires available on the HERO Registry online portal.
This collection contains 39 sets of data from over 50,000 HERO Registry members. Datasets represent separate surveys with distinct survey designs and sampling criteria. Surveys focused on health history, workplace experiences, COVID-19 exposure, social support, mental health, and the respondents' willingness to remain in or leave the healthcare field. Datasets 24 through 39 represent "hot topics" such as vaccines, vaccine willingness and uptake, childcare and school arrangements, and staffing shortages. Datasets for registry administration, respondent demographics, and survey eligibility criteria are also included.
2024-12-03
13.
Hispanic Established Populations for the Epidemiologic Study of the Elderly (HEPESE) Wave 7, 2010-2011 [Arizona, California, Colorado, New Mexico, and Texas] (ICPSR 36537)
Markides, Kyriakos; Chen, Nai-Wei; Angel, Ronald; Palmer, Raymond; Graham, James
Markides, Kyriakos; Chen, Nai-Wei; Angel, Ronald; Palmer, Raymond; Graham, James
The Hispanic EPESE provides data on risk factors for mortality and morbidity in Mexican Americans in order to contrast how these factors operate differently in non-Hispanic White Americans, African Americans, and other major ethnic groups.
The Wave 7 dataset comprises the sixth follow-up of the baseline Hispanic EPESE (HISPANIC ESTABLISHED POPULATIONS FOR THE EPIDEMIOLOGIC STUDIES OF THE ELDERLY, 1993-1994: [ARIZONA, CALIFORNIA, COLORADO, NEW MEXICO, AND TEXAS] [ICPSR 2851]). The baseline Hispanic EPESE collected data on a representative sample of community-dwelling Mexican Americans, aged 65 years and older, residing in the five southwestern states of Arizona, California, Colorado, New Mexico, and Texas.
The public-use data cover demographic characteristics (age, sex, type of Hispanic race, income, education, marital status, number of children, employment, and religion), height, weight, social and physical functioning, chronic conditions, related health problems, health habits, self-reported use of dental, hospital, and nursing home services, and depression. Subsequent follow-ups provide a cross-sectional examination of the predictors of mortality, changes in health outcomes, and institutionalization, and other changes in living arrangements, as well as changes in life situations and quality of life issues.
During this 7th Wave (dataset 1), 2010-2011, re-interviews were conducted either in person or by proxy, with 659 of the original respondents. This Wave also includes 419 re-interviews from the additional sample of Mexican Americans aged 75 years and over with higher average-levels of education than those of the surviving cohort who were added in Wave 5, increasing the total number of respondents to 1,078.
The Wave 7 Informant Interviews dataset (dataset 2) includes data which corresponds to the sixth follow-up of the baseline Hispanic EPESE Wave 7 and included re-interviews with 1,078 Mexican Americans aged 80 years and older. During these interviews, participants were asked to provide the name and contact information of the person they are "closer to" or they "depend on the most for help." These INFORMANTS were contacted and interviewed regarding the health, function, social situation, finances, and general well-being of the ongoing Hispanic EPESE respondents. Information was also collected on the informant's health, function, and caregiver responsibilities and burden. This dataset includes information from 925 informants, more than two-thirds of whom were children of the respective respondents.
2016-12-05
14.
The Irish Longitudinal Study on Ageing (TILDA), COVID-19 Study, 2020 (ICPSR 38681)
Kenny, Rose Anne; Ward, Mark
Kenny, Rose Anne; Ward, Mark
The TILDA Series data, including studies 34315, 38681, 37105, 37106, 38670, 38674, are currently unavailable at the request of the data producer due to concerns related to EU and Irish data privacy and data sharing rules. We are working to determine the best solution to continue to share these data with the research community. Individuals interested in obtaining TILDA data access at this time should reach out to the TILDA project directly (https://tilda.tcd.ie/data/accessing-data/).
The Irish Longitudinal Study on Ageing (TILDA) collects information on all aspects of health, economic and social circumstances from adults aged 50 years and over who reside in Ireland. Waves of data collection take place every two years. TILDA provides a comprehensive and accurate picture of the characteristics, needs and contributions of older persons in Ireland to inform and support improvements in policy and practice; advancements in technology and innovation; tailored education and training through an enhanced ageing research infrastructure; harmonisation with leading international research to ensure adoption of best policy and practice and comparability of results. TILDA is necessary to act as the foundation on which we can plan appropriate health, medical, social and economic policies for our older adults.
Participants were invited to complete the COVID Self Completion Questionnaire to capture their experiences during the COVID-19 pandemic. This data collection was planned in response to the pandemic and took place during the time when Wave 6 fieldwork was originally scheduled to take place.
The TILDA COVID-19 Study covers a range of aspects of the lives of adults aged 60 years and older during the first few months of the pandemic. As well as information on changes to normal day activities due to social-distancing and other restrictions on social interactions, we examine how these alterations to peoples' lives have impacted on their physical and mental wellbeing. The study also records peoples' exposure to the virus as well as that of their families and friends.
2023-03-23
15.
Jobs II Preventive Intervention for Unemployed Job Seekers, 1991-1993: [Southeast Michigan] (ICPSR 2739)
Vinokur, Amiram D.; Price, Richard H.
Vinokur, Amiram D.; Price, Richard H.
These data explore the impact of job loss and unemployment
on workers' stress and mental health, and evaluate the potential
benefits of participation in a job-search skills seminar. Respondents
were recruited from four offices of the Michigan Employment Security
Commission (MESC) in southeastern Michigan. A group of 31,560
unemployed persons were approached for the study. Of these, about
23,000 failed to meet basic initial criteria because they were new
entrants to the labor market, already re-employed, or just
accompanying others in line. Respondents were kept in the pool if they
were not on strike and not expecting to be recalled for work in the
next few months or planning to retire in the next two years. The
resulting group of 7,956 were then assessed for symptoms of depression
and willingness to participate in a job-seeking skills seminar. These
final exclusion criteria resulted in a pool of 3,402. A screening
questionnaire (Part 1) was administered to that pool, which allowed
the researchers to classify respondents as being at high risk for
depression and anxiety or at low risk. All of the high-risk
respondents and a random sample of the low-risk participants were
invited to participate in the study and in the MESC's Job
Opportunities and Basic Skills II (JOBSII) intervention program, which
consisted of a set of job-search skills seminars. JOBS II was
patterned after JOBS I, which was offered by the MESC in the late
1980s. A pretest questionnaire (Part 2) was mailed to respondents
between February and July 1991, two weeks prior to the invitation to
participate in the JOBS intervention seminar. The questionnaire
addressed the situation surrounding the respondents' loss of
employment, quality of work life in previous job, level of economic
hardship, attitudes toward obtaining a new job, social support
network, self-esteem, feelings of anxiety and/or depression, health
problems, and substance abuse history and related problems. At the
same time, a mail questionnaire was sent to each respondent's
significant other (Part 6). Items in this questionnaire focused on the
length of their relationship with the respondent, the level of support
given to the respondent, the significant other's observations
regarding the daily activities of the respondent during this period of
job loss, the significant other's feelings of anxiety and/or
depression, and the significant other's level of economic hardship. A
second and third mail questionnaire were sent six weeks (Part 3) and
six months (Part 4) after the respondents' participation in a JOBS
intervention program job-seeking skills seminar. For those respondents
who had gained employment, questions were asked regarding current
employment status, sense of job permanence, employee benefits, and
feelings toward current job. Those respondents still seeking
employment were queried about their intention to continue their job
search, job-seeking behaviors, confidence in their ability to obtain a
job, and the presence or lack of a social support network. For those
respondents still unemployed six months after the intervention
seminar, additional questions covered receipt of unemployment benefits
and how necessary those benefits were. Similarly, significant others
were queried both six weeks (Part 7) and six months (Part 8) after the
respondents' participation in the job intervention. Topics focused on
their relationship with the respondent, the observed daily activities
of the respondent, the emotional support given to the respondent, the
respondent's job-seeking behavior, the respondent's and significant
other's feelings of anxiety and/or depression, and the level of shared
responsibility regarding the payment of bills and other economic
hardships. Finally, respondents were questioned through a mail survey
two years (Part 5) after their participation in the intervention
seminar about ,their employment status, quality of work life, financial
strain endured, social support system, relationship satisfaction,
self-esteem, feelings of anxiety and/or depression, health, and sense
of control. Significant others were also queried after two years (Part
9) regarding their relationship with the respondent, the significant
other's familiarity with the respondent's feelings of anxiety and/or
depression, their social support network, and the significant other's
feelings of anxiety and/or depression. Background information on
respondents includes age, sex, race, Hispanic descent, education,
marital status, age of children in household, number of financial
dependents, and household income. Background information on
significant others includes age, sex, race, Hispanic descent,
education, and employment status. Following the conclusion of the JOBS
intervention program, respondents were asked to complete a mail
questionnaire (Part 10) evaluating the effectiveness of the program
agenda and assessing the relevance of the seminar to their job search,
the effectiveness of the seminar trainers, inoculation against
setbacks, impact on their self-esteem, effect on their interviewing
skills, and resume preparedness.
2006-01-12
16.
Katrina@10: Katrina Impacts on Vietnamese Americans in New Orleans (KATIVA NOLA) Subsample, Louisiana, 2005-2019 (ICPSR 39340)
VanLandingham, Mark Jennings; Abramson, David M.; Waters, Mary C.
VanLandingham, Mark Jennings; Abramson, David M.; Waters, Mary C.
The NIH-funded Katrina@10 Program consists of an interrelated set of three primary data collection projects that focus on specific sub-populations who were uniquely affected by Hurricane Katrina: households along Louisiana and Mississippi's Gulf Coast, low-income parents from New Orleans, and Vietnamese families living in New Orleans. In addition, the program contains two secondary analyses of data that are more broadly representative of the overall affected population, and three cores (Administrative, Data Collection, Data Management and Dissemination) to support the set of research projects. The following research questions represent the studies together as a whole:
How well does the Socio-ecological model of Disaster Recovery developed by the research team (Abraham et al. 2010) predict recovery across the three cohort studies?
How do trajectories of long-term recovery differ among and within these sub-populations?
How do the trajectories of recovery compare to those of mainstream populations?
How do the effects of pre-disposing factors (such as poverty) and degree-of-impact (such as flooding depth) vary among the three sub-populations?
How do interpretations of the disaster, resilience, and recovery differ among respondents?
What are the determinants of long-term recovery in domains such as mental and physical health, socio-economic status, and community and social roles? How are these domains related to each other across individuals and across sub-populations?
The Katrina Impacts on Vietnamese Americans in New Orleans (KATIVA NOLA) study was a longitudinal study interested in measuring the impact of Hurricane Katrina on Vietnamese-Americans living in New Orleans. The original sample was taken in summer 2005 and was followed by three rounds of short and medium-term data collection in the 5 years following Katrina. This study measured a variety of outcomes, including physical and mental health, economic stability, housing stability, and social ties, to examine the long-term recovery trajectories of participants.
The data in this collection are from an additional, long-term follow-up survey conducted between 2017 and 2019. A public-use version (DS1) and restricted-use version (DS2) are available. Open-ended responses, continuous respondent age, continuous total household income, and a variable indicating exposure to specific flood events have been masked in the public-use version. These items are available in the restricted-use version.
2025-06-24
17.
The Loma Prieta Earthquake Study examined the five-county San Francisco Bay area affected by the earthquake on October 17, 1989. Residents were asked about their experiences during, and responses to, the Loma Prieta Earthquake, measuring 6.9 on the Richter magitude scale. Telephone interviews were conducted with approximately 700 adult residents of Alameda, Santa Clara, Santa Cruz, San Mateo, and San Francisco Counties. Information was collected on topics such as evacuation, personal property damage, disaster/emergency planning and preparedness, and emotional distress as a result of the earthquake experience. Demographic variables include gender, age, income, ethnicity, religious preference, home ownership status, education level, marital status, employment status and industry, and area of the five counties where the respondent resided.
2013-05-14
18.
The Longitudinal Study of Older People in Anhui Province, China, 2001-2003 (ICPSR 36388)
Silverstein, Merril; Li, Shuzhou
Silverstein, Merril; Li, Shuzhou
The Longitudinal Study of Older People in Anhui Province, China, 2001-2003 examined the physical and psychological well-being of older adults (aged 60 and above) living in rural Anhui Province, China. The original purpose of the study was to study the impact of rural-to-urban migration on the physical and psychological well-being of older adults left behind in rural villages by their adult children.
This collection contains two parts; Part 1: 2001 Survey and Part 2: 2003 Follow-up Survey. Similar Questions were asked in the two surveys to assess intergenerational transfers and relations of the respondents, including social support, caregiving, emotional cohesion, remittances, grandchild care, and filial piety. Respondents were also asked about their health status (physical, emotional, and cognitive). Demographic information includes age, sex, marriage status, and education.
2016-05-16
19.
#MeToo Tweet IDs, October 15-28, 2017 (ICPSR 37447)
Gallagher, Ryan J.; Stowell, Elizabeth; Parker, Andrea G.; Foucault Welles, Brooke
Gallagher, Ryan J.; Stowell, Elizabeth; Parker, Andrea G.; Foucault Welles, Brooke
This collection of tweet IDs pertains to the first two weeks of the #MeToo hashtag campaign in October 2017. During this time period there were over 1.5 million tweets with the #MeToo hashtag. Tweets containing the hashtag #MeToo were collected retroactively from a full historical Twitter Firehose (100%) collection, and reply threads in response to those tweets were separately collected from Twitter. According to Twitter Terms of Service, full tweet objects cannot be disseminated, but the tweet IDs can be rehydrated through Twitter's public GET statuses/lookup API endpoint.
The available data for this study exist in one zipped folder containing 28 files. There are 14 .csv files, one for each day, between October 15th to October 28th, containing the tweet ID with one tweet ID appearing per line. Each file only contains a single column of data (
tweet_id
). There were on average 109,237 tweets per day during this two-week period ranging between 16,074 to 528,143 tweets per day. Tweets must have been public and not deleted or taken down at the time of collection in order to appear in this dataset.
The other 14 .csv files correspond to the reply threads for each day in response to tweets containing the hashtag #MeToo. Each line indicates the tweet ID of a reply in a thread of replies to a #MeToo tweet (
tweet_id
) and the tweet ID of the tweet immediately preceeding that tweet in the reply thread (
in_reply_to_tweet_id
) as comma-separated values. There were on average 21,072 replies to tweets per day during this period with a range of 2,388 to 110,789 replies per day.
2019-11-14
20.
National Elder Mistreatment Study: 8-Year Follow-up of Victims and Matched Non-Victims, United States, 2015-2018 (ICPSR 37275)
Acierno, Ronald
Acierno, Ronald
The purpose of the completed project was to follow the first National Elder Mistreatment Study, which provided prevalence estimates, with a second study of a subset of the same participants to measure the effects of elder abuse in terms of (1) health and mental health outcomes and (2) criminal justice system participation and satisfaction, as well as to specify additional predictors of these effects. Data were collected from 774 older adults 8 years following their participation in Wave I of the NEMS. This represented the results of contacting every locatable participant who reported psychological, physical, or sexual (but not financial) abuse at Wave I (achieved subsample n = 183 of the original 753 Wave I victims) and a comparison sample of 591 randomly selected Wave I non-victims from the remaining 2,149 working phone numbers of the original 5,024 non-victims (at Wave I). As mentioned, financial abuse classification at Wave I was not used to identify the victim subgroup prior to sampling, however retrospective analysis indicated that the two aforementioned sampling groups (every working phone number of Wave I victims of psychological, physical, and sexual abuse AND every working phone number of the 2,149 comparison Wave I participants) accounted for all but 7 financial abuse victims identified as such at Wave I (i.e., no other financial abuse victims at Wave I could have possibly been re-contacted). The cooperation rate (upon contact), for Wave I victims of psychological, physical, or sexual abuse was 66%; the cooperation rate of comparison Wave I participants was 57%. (Note: it had originally been proposed to conduct propensity matching once the sample of Wave I victims was re-contacted, however by conserving funds during this first phase, the study was able to expand from propensity matching to random selection of a much larger group of over 2,149, for a final derived sample of 774.)
2019-11-26
21.
National Health and Nutrition Examination Survey (NHANES), 1999-2000 (ICPSR 25501)
United States Department of Health and Human Services. Centers for Disease Control and Prevention. National Center for Health Statistics
United States Department of Health and Human Services. Centers for Disease Control and Prevention. National Center for Health Statistics
The National Health and Nutrition Examination Surveys (NHANES) is a program of studies designed to assess the health and nutritional status of adults and children in the United States. The NHANES combines personal interviews and physical examinations, which focus on different population groups or health topics. These surveys have been conducted by the National Center for Health Statistics (NCHS) on a periodic basis from 1971 to 1994. In 1999 the NHANES became a continuous program with a changing focus on a variety of health and nutrition measurements which were designed to meet current and emerging concerns. The surveys examine a nationally representative sample of approximately 5,000 persons each year. These persons are located in counties across the United States, 15 of which are visited each year. The 1999-2000 NHANES contains data for 9,965 individuals (and MEC examined sample size of 9,282) of all ages. Many questions that were asked in NHANES II, 1976-1980, Hispanic HANES 1982-1984, and NHANES III, 1988-1994, were combined with new questions in the NHANES 1999-2000.
The 1999-2000 NHANES collected data on the prevalence of selected chronic conditions and diseases in the population and estimates for previously undiagnosed conditions, as well as those known to and reported by respondents. Risk factors, those aspects of a person's lifestyle, constitution, heredity, or environment that may increase the chances of developing a certain disease or condition, were examined. Data on smoking, alcohol consumption, sexual practices, drug use, physical fitness and activity, weight, and dietary intake were collected. Information on certain aspects of reproductive health, such as use of oral contraceptives and breastfeeding practices, were also collected. The interview includes demographic, socioeconomic, dietary, and health-related questions. The examination component consists of medical, dental, and physiological measurements, as well as laboratory tests. Demographic data file variables are grouped into three broad categories: (1) Status Variables: Provide core information on the survey participant. Examples of the core variables include interview status, examination status, and sequence number. (Sequence number is a unique ID assigned to each sample person and is required to match the information on this demographic file to the rest of the NHANES 1999-2000 data). (2) Recoded Demographic Variables: The variables include age (age in months for persons through age 19 years, 11 months; age in years for 1-84 year olds, and a top-coded age group of 85+ years), gender, a race/ethnicity variable, an education variable (high school, and more than high school education), country of birth (United States, Mexico, or other foreign born), and pregnancy status variable. Some of the groupings were made due to limited sample sizes for the two-year dataset. (3) Interview and Examination Sample Weight Variables: Sample weights are available for analyzing NHANES 1999-2000 data. For a complete listing of survey contents for all years of the NHANES see the document -- Survey Content -- NHANES 1999-2010.
2012-02-22
22.
National Health and Nutrition Examination Survey (NHANES), 2001-2002 (ICPSR 25502)
United States Department of Health and Human Services. Centers for Disease Control and Prevention. National Center for Health Statistics
United States Department of Health and Human Services. Centers for Disease Control and Prevention. National Center for Health Statistics
The National Health and Nutrition Examination Surveys (NHANES) is a program of studies designed to assess the health and nutritional status of adults and children in the United States. The NHANES combines personal interviews and physical examinations, which focus on different population groups or health topics. These surveys have been conducted by the National Center for Health Statistics (NCHS) on a periodic basis from 1971 to 1994. In 1999 the NHANES became a continuous program with a changing focus on a variety of health and nutrition measurements which were designed to meet current and emerging concerns. The surveys examine a nationally representative sample of approximately 5,000 persons each year. These persons are located in counties across the United States, 15 of which are visited each year. The 2001-2002 NHANES contains data for 11,039 individuals (and MEC examined sample size of 10,477) of all ages. Many questions that were asked in NHANES II, 1976-1980, Hispanic HANES 1982-1984, and NHANES III, 1988-1994, were combined with new questions in the NHANES 2001-2002. As in past health examination surveys, data were collected on the prevalence of chronic conditions in the population. Estimates for previously undiagnosed conditions, as well as those known to and reported by survey respondents, are produced through the survey. Risk factors, those aspects of a person's lifestyle, constitution, heredity, or environment that may increase the chances of developing a certain disease or condition, were examined. Data on smoking, alcohol consumption, sexual practices, drug use, physical fitness and activity, weight, and dietary intake were collected. Information on certain aspects of reproductive health, such as use of oral contraceptives and breastfeeding practices, were also collected. The diseases, medical conditions, and health indicators that were studied include: anemia, cardiovascular disease, diabetes and lower extremity disease, environmental exposures, equilibrium, hearing loss, infectious diseases and immunization, kidney disease, mental health and cognitive functioning, nutrition, obesity, oral health, osteoporosis, physical fitness and physical functioning, reproductive history and sexual behavior, respiratory disease (asthma, chronic bronchitis, emphysema), sexually transmitted diseases, skin diseases, and vision. The sample for the survey was selected to represent the United States population of all ages. Special emphasis in the 2001-2002 NHANES was on adolescent health and the health of older Americans. To produce reliable statistics for these groups, adolescents aged 15-19 years and persons aged 60 years and older were over-sampled for the survey. African Americans and Mexican Americans were also over-sampled to enable accurate estimates for these groups. Several important areas in adolescent health, including nutrition and fitness and other aspects of growth and development, were addressed. Since the United States has experienced dramatic growth in the number of older people during the twentieth century, the aging population has major implications for health care needs, public policy, and research priorities. NCHS is working with public health agencies to increase the knowledge of the health status of older Americans. NHANES has a primary role in this endeavor. In the examination, all participants visit the physician who takes their pulse or blood pressure. Dietary interviews and body measurements are included for everyon,e. All but the very young have a blood sample taken and see the dentist. Depending upon the age of the participant, the rest of the examination includes tests and procedures to assess the various aspects of health listed above. Usually, the older the individual, the more extensive the examination. Some persons who are unable to come to the examination center may be given a less extensive examination in their homes.
Demographic data file variables are grouped into three broad categories: (1) Status Variables: provide core information on the survey participant. Examples of the core variables include interview status, examination status, and sequence number. (Sequence number is a unique ID assigned to each sample person and is required to match the information on this demographic file to the rest of the NHANES 2001-2002 data). (2) Recoded Demographic Variables: these variables include age (age in months for persons through age 19 years, 11 months; age in years for 1-84 year olds, and a top-coded age group of 85 years of age and older), gender, a race/ethnicity variable, current or highest grade of education completed, (less than high school, high school, and more than high school education), country of birth (United States, Mexico, or other foreign born), Poverty Income Ratio (PIR), income, and a pregnancy status variable (adjudicated from various pregnancy related variables). Some of the groupings were made due to limited sample sizes for the two-year data set. (3) Interview and Examination Sample Weight Variables: sample weights are available for analyzing NHANES 2001-2002 data. For a complete listing of survey contents for all years of the NHANES see the document -- Survey Content -- NHANES 1999-2010.
2012-02-22
23.
National Health and Nutrition Examination Survey (NHANES), 2003-2004 (ICPSR 25503)
United States Department of Health and Human Services. Centers for Disease Control and Prevention. National Center for Health Statistics
United States Department of Health and Human Services. Centers for Disease Control and Prevention. National Center for Health Statistics
The National Health and Nutrition Examination Surveys (NHANES) is a program of studies designed to assess the health and nutritional status of adults and children in the United States. The NHANES combines personal interviews and physical examinations, which focus on different population groups or health topics. These surveys have been conducted by the National Center for Health Statistics (NCHS) on a periodic basis from 1971 to 1994. In 1999 the NHANES became a continuous program with a changing focus on a variety of health and nutrition measurements which were designed to meet current and emerging concerns. The surveys examine a nationally representative sample of approximately 5,000 persons each year. These persons are located in counties across the United States, 15 of which are visited each year.
For NHANES 2003-2004, there were 12,761 persons selected for the sample, 10,122 of those were interviewed (79.3 percent) and 9,643 (75.6 percent) were examined in the mobile examination centers (MEC). Many of the NHANES 2003-2004 questions were also asked in NHANES II 1976-1980, Hispanic HANES 1982-1984, NHANES III 1988-1994, and NHANES 1999-2002. New questions were added to the survey based on recommendations from survey collaborators, NCHS staff, and other interagency work groups. As in past health examination surveys, data were collected on the prevalence of chronic conditions in the population. Estimates for previously undiagnosed conditions, as well as those known to and reported by survey respondents, are produced through the survey. Risk factors, those aspects of a person's lifestyle, constitution, heredity, or environment that may increase the chances of developing a certain disease or condition, were examined. Data on smoking, alcohol consumption, sexual practices, drug use, physical fitness and activity, weight, and dietary intake were collected. Information on certain aspects of reproductive health, such as use of oral contraceptives and breastfeeding practices, were also collected. The diseases, medical conditions, and health indicators that were studied include: anemia, cardiovascular disease, diabetes and lower extremity disease, environmental exposures, equilibrium, hearing loss, infectious diseases and immunization, kidney disease, mental health and cognitive functioning, nutrition, obesity, oral health, osteoporosis, physical fitness and physical functioning, reproductive history and sexual behavior, respiratory disease (asthma, chronic bronchitis, emphysema), sexually transmitted diseases, skin diseases, and vision. The sample for the survey was selected to represent the United States population of all ages. Special emphasis in the 2003-2004 NHANES was on adolescent health and the health of older Americans. To produce reliable statistics for these groups, adolescents aged 15-19 years and persons aged 60 years and older were over-sampled for the survey. African Americans and Mexican Americans were also over-sampled to enable accurate estimates for these groups. Several important areas in adolescent health, including nutrition and fitness and other aspects of growth and development, were addressed. Since the United States has experienced dramatic growth in the number of older people during the twentieth century, the aging population has major implications for health care needs, public policy, and research priorities. NCHS is working with public health agencies to increase the knowledge of the health status of old,er Americans. NHANES has a primary role in this endeavor. In the examination, all participants visit the physician who takes their pulse or blood pressure. Dietary interviews and body measurements are included for everyone. All but the very young have a blood sample taken and see the dentist. Depending upon the age of the participant, the rest of the examination includes tests and procedures to assess the various aspects of health listed above. Usually, the older the individual, the more extensive the examination. Some persons who are unable or unwilling to come to the examination center may be given a less extensive examination in their homes.
Demographic data file variables are grouped into three broad categories: (1) Status Variables: provide core information on the survey participant. Examples of the core variables include interview status, examination status, and sequence number. (Sequence number is a unique ID assigned to each sample person and is required to match the information on this demographic file to the rest of the NHANES 2003-2004 data). (2) Recoded Demographic Variables: these variables include age (age in months for persons through age 19 years, 11 months; age in years for 1- to 84-year-olds, and a top-coded age group of 85 years of age and older), gender, a race/ethnicity variable, current or highest grade of education completed, (less than high school, high school, and more than high school education), country of birth (United States, Mexico, or other foreign born), Poverty Income Ratio (PIR), income, and a pregnancy status variable (adjudicated from various pregnancy related variables). Some of the groupings were made due to limited sample sizes for the two-year data set. (3) Interview and Examination Sample Weight Variables: sample weights are available for analyzing NHANES 2003-2004 data. For a complete listing of survey contents for all years of the NHANES see the document -- Survey Content -- NHANES 1999-2010.
2016-07-11
24.
National Health and Nutrition Examination Survey (NHANES), 2005-2006 (ICPSR 25504)
United States Department of Health and Human Services. Centers for Disease Control and Prevention. National Center for Health Statistics
United States Department of Health and Human Services. Centers for Disease Control and Prevention. National Center for Health Statistics
The National Health and Nutrition Examination Surveys (NHANES) is a program of studies designed to assess the health and nutritional status of adults and children in the United States. The NHANES combines personal interviews and physical examinations, which focus on different population groups or health topics. These surveys have been conducted by the National Center for Health Statistics (NCHS) on a periodic basis from 1971 to 1994. In 1999 the NHANES became a continuous program with a changing focus on a variety of health and nutrition measurements which were designed to meet current and emerging concerns. The surveys examine a nationally representative sample of approximately 5,000 persons each year. These persons are located in counties across the United States, 15 of which are visited each year. For NHANES 2005-2006, there were 10,348 persons selected for the sample, 10,122 of those were interviewed (79.3 percent) and 9,643 (75.6 percent) were examined in the mobile examination centers (MEC). Many of the NHANES 2005-2006 questions were also asked in NHANES II 1976-1980, Hispanic HANES 1982-1984, NHANES III 1988-1994, and NHANES 1999-2004. New questions were added to the survey based on recommendations from survey collaborators, NCHS staff, and other interagency work groups. As in past health examination surveys, data were collected on the prevalence of chronic conditions in the population. Estimates for previously undiagnosed conditions, as well as those known to and reported by survey respondents, are produced through the survey. Risk factors, those aspects of a person's lifestyle, constitution, heredity, or environment that may increase the chances of developing a certain disease or condition, were examined. Data on smoking, alcohol consumption, sexual practices, drug use, physical fitness and activity, weight, and dietary intake were collected. Information on certain aspects of reproductive health, such as use of oral contraceptives and breastfeeding practices, were also collected. The diseases, medical conditions, and health indicators that were studied include: anemia, cardiovascular disease, diabetes and lower extremity disease, environmental exposures, equilibrium, hearing loss, infectious diseases and immunization, kidney disease, mental health and cognitive functioning, nutrition, obesity, oral health, osteoporosis, physical fitness and physical functioning, reproductive history and sexual behavior, respiratory disease (asthma, chronic bronchitis, emphysema), sexually transmitted diseases, skin diseases, and vision. The sample for the survey was selected to represent the United States population of all ages. Special emphasis in the 2005-2006 NHANES was on adolescent health and the health of older Americans. To produce reliable statistics for these groups, adolescents aged 15-19 years and persons aged 60 years and older were over-sampled for the survey. African Americans and Mexican Americans were also over-sampled to enable accurate estimates for these groups. Several important areas in adolescent health, including nutrition and fitness and other aspects of growth and development, were addressed. Since the United States has experienced dramatic growth in the number of older people during the twentieth century, the aging population has major implications for health care needs, public policy, and research priorities. NCHS is working with public health agencies to increase the knowledge of the health status of older Americans,. NHANES has a primary role in this endeavor. In the examination, all participants visit the physician who takes their pulse or blood pressure. Dietary interviews and body measurements are included for everyone. All but the very young have a blood sample taken and see the dentist. Depending upon the age of the participant, the rest of the examination includes tests and procedures to assess the various aspects of health listed above. Usually, the older the individual, the more extensive the examination. Some persons who are unable or unwilling to come to the examination center may be given a less extensive examination in their homes.
Demographic data file variables are grouped into three broad categories: (1) Status Variables: provide core information on the survey participant. Examples of the core variables include interview status, examination status, and sequence number. (Sequence number is a unique ID assigned to each sample person and is required to match the information on this demographic file to the rest of the NHANES 2005-2006 data). (2) Recoded Demographic Variables: these variables include age (age in months for persons through age 19 years, 11 months; age in years for 1- to 84-year-olds, and a top-coded age group of 85 years of age and older), gender, a race/ethnicity variable, current or highest grade of education completed, (less than high school, high school, and more than high school education), country of birth (United States, Mexico, or other foreign born), Poverty Income Ratio (PIR), income, and a pregnancy status variable (adjudicated from various pregnancy related variables). Some of the groupings were made due to limited sample sizes for the two-year dataset. (3) Interview and Examination Sample Weight Variables: sample weights are available for analyzing NHANES 2005-2006 data. For a complete listing of survey contents for all years of the NHANES see the document -- Survey Content -- NHANES 1999-2010.
2012-02-22
25.
National Health and Nutrition Examination Survey (NHANES), 2007-2008 (ICPSR 25505)
United States Department of Health and Human Services. Centers for Disease Control and Prevention. National Center for Health Statistics
United States Department of Health and Human Services. Centers for Disease Control and Prevention. National Center for Health Statistics
The National Health and Nutrition Examination Surveys (NHANES) is a program of studies designed to assess the health and nutritional status of adults and children in the United States. The NHANES combines personal interviews and physical examinations, which focus on different population groups or health topics. These surveys have been conducted by the National Center for Health Statistics (NCHS) on a periodic basis from 1971 to 1994. In 1999 the NHANES became a continuous program with a changing focus on a variety of health and nutrition measurements which were designed to meet current and emerging concerns. The surveys examine a nationally representative sample of approximately 5,000 persons each year. These persons are located in counties across the United States, 15 of which are visited each year. For NHANES 2007-2008, there were 12,946 persons selected for the sample, 10,149 of those were interviewed (78.4 percent) and 9,762 (75.4 percent) were examined in the mobile examination centers (MEC). Many of the NHANES 2007-2008 questions were also asked in NHANES II 1976-1980, Hispanic HANES 1982-1984, NHANES III 1988-1994, and NHANES 1999-2006. New questions were added to the survey based on recommendations from survey collaborators, NCHS staff, and other interagency work groups. As in past health examination surveys, data were collected on the prevalence of chronic conditions in the population. Estimates for previously undiagnosed conditions, as well as those known to and reported by survey respondents, are produced through the survey. Risk factors, those aspects of a person's lifestyle, constitution, heredity, or environment that may increase the chances of developing a certain disease or condition, were examined. Data on smoking, alcohol consumption, sexual practices, drug use, physical fitness and activity, weight, and dietary intake were collected. Information on certain aspects of reproductive health, such as use of oral contraceptives and breastfeeding practices, were also collected. The diseases, medical conditions, and health indicators that were studied include: anemia, cardiovascular disease, diabetes and lower extremity disease, environmental exposures, equilibrium, hearing loss, infectious diseases and immunization, kidney disease, mental health and cognitive functioning, nutrition, obesity, oral health, osteoporosis, physical fitness and physical functioning, reproductive history and sexual behavior, respiratory disease (asthma, chronic bronchitis, emphysema), sexually transmitted diseases, skin diseases, and vision. The sample for the survey was selected to represent the United States population of all ages. The NHANES target population is the civilian, noninstitutionalized United States population. Beginning in 2007, some changes were made to the domains being oversampled. The primary change is the oversampling of the entire Hispanic population instead of just the Mexican American (MA) population, which has been oversampled since 1988. Sufficient numbers of MAs were retained in the sample design so that trends in the health of MAs can continue to be monitored. Persons 60 years of age and older, Blacks, and low income persons were also oversampled. In addition, for each of the race/ethnicity domains, the 12-15 and 16-19 year age domains were combined and the 40-59 year age minority domains were split into 10-year age domains of 40-49 and 50-59. This has led to an increase in the number of participants aged 40 and older and, a decrease in 12- to 19-year-olds from previous cycles. The oversample of pregnant women and adolescents in the survey from 1999-2006 was discontinued to allow for the oversampling of the Hispanic population. NCHS is working with public health agencies to increase knowledge of the health status of older Americans. NHANES has a primary role in this endeavor. In the examination, all participants visit the physician who takes their pulse or blood pressure. Dietary interviews and body measurements are included for everyone. All but the very young have a blood sample taken and see the dentist. Depending upon the age of the participant, the rest of the examination includes tests and procedures to assess the various aspects of health listed above. Usually, the older the individual, the more extensive the examination.
Demographic data file variables are grouped into three broad categories: (1)
Status Variables: Provide core information on the survey participant. Examples
of the core variables include interview status, examination status, and
sequence number. (Sequence number [SEQN] is a unique ID number assigned to each
sample person and is required to match the information on this demographic file
to the rest of the NHANES 2007-2008 data.) (2) Recoded Demographic Variables:
The variables include age (age in months for persons under age 80, age in years
for 1 to 80-year-olds, and a top-coded age group of 80 years and older), gender, a
race/ethnicity variable, an current or highest grade of education completed,
(less than high school, high school, and more than high school education),
country of birth (United States, Mexico, or other foreign born), ratio of
family income to poverty threshold, income, and a pregnancy status variable
(adjudicated from various pregnancy-related variables). Some of the groupings
were made due to limited sample sizes for the two-year dataset. (3) Interview and
Examination Sample Weight Variables: Sample weights are available for
analyzing NHANES 2007-2008 data. Most data analyses require either the
interviewed sample weight (variable name: WTINT2YR) or examined sample weight
(variable name: WTMEC2YR). The two-year sample weights (WTINT2YR, WTMEC2YR)
should be used for NHANES 2007-2008 analyses.
2012-02-22
26.
National Longitudinal Study of Adolescent to Adult Health (Add Health) Parent Study: Public Use, [United States], 2015-2017 (ICPSR 37375)
Harris, Kathleen Mullan; Hotz, V. Joseph
Harris, Kathleen Mullan; Hotz, V. Joseph
The National Longitudinal Study of Adolescent to Adult Health (Add Health) Parent Study Public Use collection includes data gathered as part of the Add Health longitudinal survey of adolescents. The original Add Health survey is a longitudinal study of a nationally representative sample of adolescents in grades 7-12 in the United States during the 1994-1995 school year. In Wave 1 of the Add Health Study (1994-1995), a parent of each Add Health Sample Member (AHSM) was interviewed. The Add Health Parent Study gathered social, behavioral, and health survey data in 2015-2017 from the parents of Add Health Sample members who were originally interviewed at Wave 1 (1994-1995). Wave 1 Parents were asked about their adolescent children, their relationships with them, and their own health.
The Add Health Parent Study interview is a comprehensive survey of Add Health parents' family relations, education, religious beliefs, physical and mental health, social support, and community involvement experiences. In addition, survey data contains cognitive assessments, a medications log linked to a medications database lookup table, and household financial information collection. The survey also includes permission for administrative data linkages and includes data from a Family Health History Leave-Behind questionnaire. Interviews were conducted with parents' spouse/partner when available.
Research domains targeted in the survey and research questions that may be addressed using the Add Health Parent Study data include:
Health Behaviors and Risks
Many health conditions and behaviors run in families; for example, cardiovascular disease, obesity and substance abuse. How are health risks and behaviors transmitted across generations or clustered within families? How can we use information on the parents' health and health behavior to better understand the determinants of their (adult) children's health trajectories?
Cognitive Functioning and Non-Cognitive Personality Traits
What role does the intergenerational transmission of personality and locus of control play in generating intergenerational persistence in education, family status, income and health? How do the personality traits of parents and children, and how they interact, influence the extent and quality of intergenerational relationships and the prevalence of assistance across generations?
Decision-Making, Expectations, and Risk Preferences
Do intergenerational correlations in risk preferences represent intergenerational transmission of preferences? If so, are the transmission mechanisms a factor in biological and environmental vulnerabilities? Does the extent of genetic liability vary in response to both family-specific and generation-specific environmental pressures?
Family Support, Relationship Quality and Ties of Obligation
How does family complexity affect intergenerational obligations and the strength of relationship ties? As parents near retirement: What roles do they play in their children's lives and their children in their lives? What assistance are they providing to their adult children and grandchildren? What do they receive in return? And how do these ties vary with divorce, remarriage and familial estrangement?
Economic Status and Capacities
What are the economic capacities of the parents' generation as they reach their retirement years? How have far,ed through the wealth and employment shocks of the Great Recession? Are parents able to provide for their own financial need? And, do they have the time and financial resources to help support their children and grandchildren and are they prepared to do so?
2020-08-10
27.
National Social Life, Health, and Aging Project (NSHAP): Round 3 and COVID-19 Study, [United States], 2015-2016, 2020-2021 (ICPSR 36873)
Waite, Linda J.; Cagney, Kathleen A.; Dale, William; Hawkley, Louise C.; Huang, Elbert S.; Lauderdale, Diane S.; Laumann, Edward O.; McClintock, Martha K.; O'Muircheartaigh, Colm A.; Schumm, L. Philip
Waite, Linda J.; Cagney, Kathleen A.; Dale, William; Hawkley, Louise C.; Huang, Elbert S.; Lauderdale, Diane S.; Laumann, Edward O.; McClintock, Martha K.; O'Muircheartaigh, Colm A.; Schumm, L. Philip
The National Social Life, Health and Aging Project (NSHAP) is a population-based study of health and social factors on a national scale, aiming to understand the well-being of older, community-dwelling Americans by examining the interactions among physical health, illness, medication use, cognitive function, emotional health, sensory function, health behaviors, and social connectedness. It is designed to provide health providers, policy makers, and individuals with useful information and insights into these factors, particularly on social and intimate relationships.
The National Opinion Research Center (NORC), along with Principal Investigators at the University of Chicago, conducted more than 3,000 interviews during 2005 and 2006 with a nationally representative sample of adults aged 57 to 85. Face-to-face interviews and biomeasure collection took place in respondents' homes. Round 3 was conducted from September 2015 through November 2016, where 2,409 surviving Round 2 respondents were re-interviewed, and a New Cohort consisting of adults born between 1948 and 1965 together with their spouses or co-resident partners was added. All together, 4,777 respondents were interviewed in Round 3. The following files constitute Round 3: Core Data, Social Networks Data, Disposition of Returning Respondent Partner Data, and Proxy Data.
Included in the Core files (Datasets 1 and 2) are demographic characteristics, such as gender, age, education, race, and ethnicity. Other topics covered respondents' social networks, social and cultural activity, physical and mental health including cognition, well-being, illness, history of sexual and intimate partnerships and patient-physician communication, in addition to bereavement items. In addition data on a panel of biomeasures including, weight, waist circumference, height, and blood pressure was collected. The Social Networks (Datasets 3 and 4) files detail respondents' current relationship status with each person identified on the network roster. The Disposition of Returning Respondent Partner (Datasets 5 and 6) files detail information derived from Section 6A items regarding the partner from Rounds 1 and 2 within the questionnaire. This provides a complete history for respondent partners across both rounds. The Proxy (Datasets 7 and 8) files contain final health data for Round 1 and Round 2 respondents who could not participate in NSHAP due to disability or death.
The COVID-19 sub-study, administered to NSHAP R3 respondents in the Fall of 2020, was a brief self-report questionnaire that probed how the coronavirus pandemic changed older adults' lives. The COVID-19 sub-study questionnaire was limited to assessing specific domains in which respondents may have been affected by the coronavirus pandemic, including: (1) COVID experiences, (2) health and health care, (3) job and finances, (4) social support, (5) marital status and relationship quality, (6) social activity and engagement, (7) living arrangements, (8) household composition and size, (9) mental health, (10) elder mistreatment, (11) health behaviors, and (12) positive impacts of the coronavirus pandemic. Questions about engagement in racial justice issues since the death of George Floyd in police custody were also added to facilitate analysis of the independent and compounding effects of both the COVID-19 pandemic and reckoning with longstanding racial injustice in America.
2024-09-09
28.
National Survey of American Life - Adolescent Supplement (NSAL-A), 2001-2004 (ICPSR 36380)
Jackson, James S. (James Sidney); Caldwell, Cleopatra H.; Antonucci, Toni C.; Oyserman, Daphna R.
Jackson, James S. (James Sidney); Caldwell, Cleopatra H.; Antonucci, Toni C.; Oyserman, Daphna R.
The National Survey of American Life Adolescent Supplement (NSAL-A), 2001-2004, was designed to estimate the lifetime-to-date and current prevalence, age-of-onset distributions, course, and comorbidity of DSM-IV disorders among African American and Caribbean adolescents in the United States; to identify risk and protective factors for the onset and persistence of these disorders; to describe patterns and correlates of service use for these disorders; and to lay the groundwork for subsequent follow-up studies that can be used to identify early expressions of adult mental disorders. In addition and similar to the NSAL adult dataset (Collaborative Psychiatric Epidemiology Surveys (CPES), 2001-2003 [United States] (ICPSR 20240)), the adolescent dataset contains detailed measures of health; social conditions; stressors; distress; racial identity; subjective, neighborhood conditions; activities and school; media; and social and psychological protective and risk factors. Numerous variables from the adult dataset have been merged into the adolescent dataset, as the NSAL adult and adolescent respondents reside in the same households. Some of these variables apply to the entire household (i.e. region, urbanicity, and family income), while others apply specifically to the NSAL adult respondent living in the adolescent's household (i.e. adult years of education, adult marital status, and adult nativity [foreign-born vs. US born]). The immigration measures were asked of Caribbean black adult respondents only. No comparable measures assess the immigration and generational status of the Caribbean black adolescent respondents. The adult dataset measures are merged into the adolescent dataset to assist in approximating these measures for adolescent respondents. The NSAL adolescent dataset also includes variables for other non-core and experimental disorders. These include tobacco use/nicotine dependence, premenstrual syndrome, minor depression, recurrent brief depression, hypomania, and hypomania sub-threshold. Demographic variables include age, race and ethnicity, ancestry or national origins, height, weight, marital status, income, and education level.
2016-07-28
29.
Since 2013, the Robert Wood Johnson Foundation (RWJF) has led the development of a pioneering national action framework to advance a "culture that enables all in our diverse society to lead healthier lives now and for generations to come." Accomplishing these principles requires a national paradigm shift from a traditionally disease and health care-centric view of health toward one that focuses on well-being. Recognizing that paradigm shifts require intentional actions, RWJF worked with RAND researchers to design an actionable path to fulfill the Culture of Health (CoH) vision. A central piece of this work is the development of measures to assess constructs underlying a CoH.
The National Survey of Health Attitudes is a survey that RWJF and RAND analysts developed and conducted as part of the foundation's CoH strategic framework. The foundation undertook this survey to measure key constructs that could not be measured in other data sources. Thus, the survey was not meant to capture the full action framework that informs CoH, but rather just selected measure areas. The questions in this survey primarily addressed the action area: making health a shared value. The survey covers a variety of topics, including views regarding what factors influence health, such as the notion of health interdependence (peer, family, neighborhood, and workplace drivers of health), values related to national and community investment for health and well-being; behaviors around health and well-being, including civic engagement on behalf of health, and the role of community engagement and sense of community in relation to health attitudes and values.
2021-12-14
30.
Since 2013, the Robert Wood Johnson Foundation (RWJF) has led the development of a pioneering national action framework to advance a "culture that enables all in our diverse society to lead healthier lives now and for generations to come." Accomplishing these principles requires a national paradigm shift from a traditionally disease and health care-centric view of health toward one that focuses on well-being. Recognizing that paradigm shifts require intentional actions, RWJF worked with RAND researchers to design an actionable path to fulfill the Culture of Health (CoH) vision. A central piece of this work is the development of measures to assess constructs underlying a CoH.
The National Survey of Health Attitudes is a survey that RWJF and RAND analysts developed and conducted as part of the foundation's CoH strategic framework. The foundation undertook this survey to measure key constructs that could not be measured in other data sources. Thus, the survey was not meant to capture the full action framework that informs CoH, but rather just selected measure areas. The questions in this survey primarily addressed the action area: making health a shared value. The survey covers a variety of topics, including views regarding what factors influence health, such as the notion of health interdependence (peer, family, neighborhood, and workplace drivers of health), values related to national and community investment for health and well-being; behaviors around health and well-being, including civic engagement on behalf of health, and the role of community engagement and sense of community in relation to health attitudes and values.
This study includes the results from the 2018 RWJF National Survey of Health Attitudes. This 2018 survey is considered the second wave, the first wave of the survey was conducted in 2015 (ICPSR 37405). In 2018, the study team fielded an updated version that included many of the same questions but added some new constructs that were of interest as part of the larger Culture of Health effort. This study complements the overview of the 2015 survey described in the RAND report Development of the Robert Wood Johnson Foundation National Survey of Health Attitudes (Carman et al., 2016).
2021-12-16
31.
Since 2013, the Robert Wood Johnson Foundation (RWJF) has led the development of a pioneering national action framework to advance a "culture that enables all in our diverse society to lead healthier lives now and for generations to come." Accomplishing these principles requires a national paradigm shift from a traditionally disease and health care-centric view of health toward one that focuses on well-being. Recognizing that paradigm shifts require intentional actions, RWJF worked with RAND researchers to design an actionable path to fulfill the Culture of Health (CoH) vision. A central piece of this work is the development of measures to assess constructs underlying a CoH.
The National Survey of Health Attitudes (NSHA) is a survey that RWJF and RAND analysts developed and conducted as part of the foundation's CoH strategic framework. The foundation undertook this survey to measure key constructs that could not be measured in other data sources. Thus, the survey was not meant to capture the full action framework that informs CoH, but rather just selected measure areas. The questions in this survey primarily addressed the action area: making health a shared value. The survey covers a variety of topics, including views regarding what factors influence health, such as the notion of health interdependence (peer, family, neighborhood, and workplace drivers of health), values related to national and community investment for health and well-being; behaviors around health and well-being, including civic engagement on behalf of health, and the role of community engagement and sense of community in relation to health attitudes and values.
This study includes the results from the 2023 RWJF National Survey of Health Attitudes. The 2023 survey is the third wave of the NSHA. The first wave was conducted in 2015 (ICPSR 37405) and the second wave in 2018 (ICPSR 37633). The 2023 report complements the overview of the 2015 survey described in the RAND report Development of the Robert Wood Johnson Foundation National Survey of Health Attitudes (Carman et al., 2016), and its subsequent topline 2018 Survey of National Health Attitudes: Description and Top-Line Summary (Carman et al., 2019) and is organized similarly for consistency. A companion set of longitudinal surveys during the COVID-19 pandemic was fielded between 2020 and 2021 and is further described in four top-line reports, COVID-19 and the Experiences of Populations at Greater Risk (Carman et al., 2020-2021).
The questions in the 2023 survey uniquely capture aspects of American mindset about health, health equity, structural racism, and wellbeing in ways that are not present in other surveys. This version of the NSHA can be viewed in three main sections: (1) individual health experiences, perspectives, and knowledge (making health a shared value); (2) health equity perspectives; and (3) community wellbeing, including climate views and barriers to community engagement. Insights from the surveys referenced above, including this one, have established a baseline and set of cross-sectional pulse checks on where the American public is regarding their recognition of social determinants of health, their understanding of health inequities including structural racism, their willingness to address those inequities and their indication of who in society should be responsible for solving ,health inequities.
2024-12-05
32.
Policing the Rainbow: LGBTQ Experiences, Attitudes, and Perceptions of Law Enforcement, United States, 2022 (ICPSR 39125)
Vogler, Stefan; Jenness, Valerie
Vogler, Stefan; Jenness, Valerie
Policing the Rainbow is a mixed-methods study utilizing qualitative interviews and a survey conducted through the AmeriSpeak Panel at NORC at the University of Chicago. The aim of Policing the Rainbow was to better understand the relationship between law enforcement and the LGBTQ community.
2025-05-29
33.
Project STRIDE: Stress, Identity, and Mental Health, New York City, 2004-2005 (ICPSR 35525)
Meyer, Ilan H.; Dohrenwend, Bruce Philip; Schwartz, Sharon; Hunter, Joyce; Kertzner, Robert M.
Meyer, Ilan H.; Dohrenwend, Bruce Philip; Schwartz, Sharon; Hunter, Joyce; Kertzner, Robert M.
Project STRIDE is a three-year research project that examines the effect of stress and minority identity related to sexual orientation, race/ethnicity and gender on mental health. The research describes social stressors that affect minority populations, explores the coping and social support resources that they utilize as they confront these social stressors, and assesses the associations of stress and coping with mental health outcomes including mental disorders and wellbeing. The study also explores the impact of various identity characteristics, such as whether an identity is viewed positively or negatively, or whether it is prominent or not to the relationship of stress and mental health outcomes.
The study, using extensive quantitative and some qualitative measures, is a longitudinal survey of 525 men and women between the ages 18 and 59 who are residents of New York City. Socio-demographic information collected about respondents included age, education, race and Hispanic ethnicity, adopting the measures developed and used by the United States Census Bureau in the United States population survey of 2000. In addition to these items, racial/ethnic identity was also assessed with the question "What is the country of origin related to your or your family's ethnic or national background, if any?" Respondents were allowed to select up to two nations from a comprehensive listing. For the purposes of the study, the instrument also assessed whether or not participants were natives of New York City or migrated as adults. Additional demographic variables include employment status, religion, relationship status, and sexual orientation.
2018-11-28
34.
Puerto Rican Maternal and Infant Health Study (PRMIHS), 1994-1995 (ICPSR 36238)
Landale, Nancy; Oropesa, R. Salvador; Davila, Ana Luisa
Landale, Nancy; Oropesa, R. Salvador; Davila, Ana Luisa
The Puerto Rican Maternal and Infant Health Study (PRMIHS) is a cross-sectional study designed to provide information on the determinants of poor infant health among Puerto Ricans. The dataset features personal interview data from 2,763 mothers of Puerto Rican infants sampled from the 1994 and 1995 birth and infant death records of six United States vital statistics reporting areas (Connecticut, Florida, Massachusetts, New Jersey, New York City, Pennsylvania) and the Commonwealth of Puerto Rico. Mothers were contacted to participate in a Computer Assisted Personal Interview (CAPI) using the address information provided in the birth and infant death records. Respondent mothers were asked to recount their sexual history and use of contraception, age at conception, prenatal care and nutrition, substance abuse, and overall health before and during pregnancy. Details were also collected regarding migration history, family composition, partner involvement, social support structures, and receipt of any public financial assistance for food, housing, and/or medical care. Information regarding infant health and well-being was also gathered, and included respondents' reporting of recurrent health issues, required medical treatments, immunizations, and any accidents or sustained injuries. Mothers were also asked to confirm attainment of a number of infant developmental milestones, including sitting, crawling, standing, waving, and vocalization, as well as several other behaviors and abilities. Demographic information for mothers includes age, education, occupation, income, marital status, race and ethnic identity, language, and religious preference.
2015-11-16
35.
Racial and Ethnic Differences in Youth's Mental Health and Substance Needs and Services: Findings from the Survey of Youth in Residential Placement (SYRP), United States, 2003 (ICPSR 36788)
Heaton, Leanne
Heaton, Leanne
These data are part of NACJD's Fast Track Release and are distributed as they were received from the data depositor. The files have been zipped by NACJD for release, but not checked or processed except for the removal of direct identifiers. Users should refer to the accompanying readme file for a brief description of the files available with this collection and consult the investigator(s) if further information is needed.
This study examined differences in youth's mental health and substance abuse needs in seven different racial/ethnic groups of justice-involved youth. Using de-identified data from the Survey of Youth in Residential Placement (SYRP), it was assessed whether differences in mental health and substance abuse needs and services existed in a racially/ethnically diverse sample of youth in custody. Data came from a nationally representative sample of 7,073 youth in residential placements across 36 states, representing five program types. An examination of the extent to which there were racial/ethnic disparities in the delivery of services in relation to need was also conducted. This examination included assessing the differences in substance-related problems, availability of substance services, and receipt of substance-specific counseling.
One SAS data file (syrp2017.sas7bdat) is included as part of this collection and has 138 variables for 7073 cases, with demographic variables on youth age, sex, race and ethnicity. Also included as part of the data collection are two SAS Program (syntax) files for use in secondary analysis of youth mental health and substance use.
2018-11-29
36.
Reduction of Health Disparities in Appalachians with Multiple Cardiovascular Disease Risk Factors: A Randomized Controlled Trial, 2013-2016 (ICPSR 36985)
Moser, Debra K.
Moser, Debra K.
This study consists of a two-group, randomized, controlled comparative effectiveness trial with 300 individuals from Appalachian Kentucky who do not have a primary care provider (and thus are not able to receive the standard of care without intercession) and who are at risk for CVD (cardiovascular disease) by virtue of having two or more modifiable CVD risk factors. The researchers compared (1) the standard of care alone, referral to a primary care provider for management of CVD risk factors, with (2) standard of care supplemented by patient-centered, culturally appropriate, self-care CVD risk reduction intervention (HeartHealth) designed to improve multiple CVD risk factors while overcoming barriers to success.
The researchers compared the 4 month (short-term) and 1 year (long-term) impact of the interventions on: 1) CVD risk factors selected by patients (i.e., tobacco use, blood pressure, lipid profile, HgA1c for diabetics, body mass index, waist circumference, depressive symptoms, or physical activity level); 2) all CVD risk factors for each patient; 3) quality of life; 4) patient and healthcare provider satisfaction; 5) desirability and adoptability by assessing adherence to recommended CVD risk reduction protocols, and retention of recruited individuals.
Demographic variables include gender, age, ethnicity, marital status, employment status, and level of education.
2021-07-26
37.
Social Justice Sexuality Project: 2010 National Survey, including Puerto Rico (ICPSR 34363)
Battle, Juan; Pastrana, Antonio Jay; Daniels, Jessie
Battle, Juan; Pastrana, Antonio Jay; Daniels, Jessie
The Social Justice Sexuality Project (SJS) is one of the largest national surveys of Black, Latina/o, Asian and Pacific Islander, and multiracial lesbian, gay, bisexual, and transgender (LGBT) people. With over 5,000 respondents, the final sample includes respondents from all 50 states; Washington, DC, and Puerto Rico; in rural and suburban areas, in addition to large urban areas; and from a variety of ages, racial/ethnic identities, sexual orientations, and gender identities. The purpose of the SJS Project is to document and celebrate the experiences of lesbian, gay, bisexual and transgender (LGBT) people of color. All too often, when we think about LGBT people of color, it's from a perspective of pathology. In contrast, the SJS Project is designed and dedicated to describing a more dynamic experience. It's a knowledge-based study that investigates the sociopolitical experiences of this population around five themes: racial and sexual identity; spirituality and religion; mental and physical health; family formations and dynamics; civic and community engagement. Demographic variables include: race/ethnicity, sexual orientation, gender identity, age, education, religion, household, income, height, weight, location, birthplace, and political affiliation.
Additional information about the SJS Project can be found on the Social Justice Sexuality Project Web site.
2013-08-09
38.
Stereotype Threat and Women's Work Satisfaction: The Importance of Role Models, 72 Countries (ICPSR 37189)
Cortland, Clarissa
Cortland, Clarissa
This research examines the psychological benefits of different sources of workplace social support in a global sample of professional women leaders (N = 1,221). We explored whether and in what way(s) social support from different workplace sources (role models, formal and informal mentors/sponsors, supportive supervisors, and peer support) predicts women's experience of stereotype threat - or concerns about confirming gender stereotypes - and subsequently their work satisfaction. We did this using cross-sectional data from a survey of international graduate business school alumnae who represented 72 countries, were mostly from Generation X (63.4% aged 35-54), reported directly to General Management or had more senior roles (64.1%) and described their work responsibilities as regional or global (66.4%). Workplace role models emerge as the only statistically reliable predictor of work satisfaction indirectly through reduced stereotype threat concerns. However, role models, informal (but not formal) mentors/sponsors, supportive supervisors, and peer support all directly predict women's work satisfaction. Implications of the benefits of workplace social support for efforts to reduce work-related gender inequities are discussed.
2018-11-05
39.
Stroke Recovery in Underserved Populations 2005-2006 [United States] (ICPSR 36422)
Ostir, Glenn; Ottenbacher, Kenneth; Kuo, Yong Fang
Ostir, Glenn; Ottenbacher, Kenneth; Kuo, Yong Fang
The Stroke Recovery in Underserved Populations 2005-2006 study was created to address the National Institute on Aging (NIA) Request For Application entitled "Research on Mind-Body Interactions and Health" (RFA OD-03-008). It addressed the NIA interest in "the impact of optimism, happiness, or a positive attitude on well-being and health; and social functioning and health."
The study examined how positive emotion (e.g., joy, gratitude, love, contentment) and social networks independently and interactively contribute to recovery of functional status after stroke within two underserved groups. The specific study aims were to:
Examine recovery of functional status (motor and cognitive function), for White, African American and Hispanic persons with stroke discharged from rehabilitation facilities
Examine the contributions of positive emotion and social networks on recovery of functional status (motor and cognitive function), for White, African American, and Hispanic persons with stroke discharged from rehabilitation facilities; and
Examine the interaction between positive emotion and social networks on recovery of functional status (motor and cognitive function) for White, African American, and Hispanic persons with stroke discharged from rehabilitation facilities.
The data were collected by the IT Health Track at four time points: at admission and discharge from rehabilitation facility, and 80-180 days and 365-425 days after discharge. These data emphasize recovery of motor and cognitive functional status, positive emotion, and social networks
The dataset contains 226 variables and 1219 cases from 11 rehabilitation facilities across the United States.
2016-05-03
40.
Survey of Community, Crime, and Health, 1995, 1998 [United States] (ICPSR 4381)
Ross, Catherine E.; Britt, Chester L.
Ross, Catherine E.; Britt, Chester L.
The Survey of Community, Crime, and Health (CCH) was
conducted in 1995 and 1998 in Illinois to examine the relationship
between neighborhood disadvantage and physical and mental health,
(over and above individual socio-economic characteristics), in order
to develop a measure of perceived neighborhood disorder and to explore
its role in explaining that relationship. Interviews were conducted
with 2,482 respondents and covered topics such as physical health,
mental health, health behaviors, use of services, and sense of
control. Also examined were social support, perceived neighborhood
characteristics, neighborhood social support, and personal and
household demographics. In addition to individual-level variables,
Wave I of the CCH contains a number of community-level variables that
were created from the 1990 STF Census data. Variable names starting
with T are tract-level, variables starting with C are county-level,
and variables starting with P are city-level.
2010-09-21
41.
Survey of Midlife in Japan (MIDJA 2), May-October 2012 (ICPSR 36427)
Ryff, Carol D.; Kitayama, Shinobu; Karasawa, Mayumi; Markus, Hazel; Kawakami, Norito; Coe, Christopher
Ryff, Carol D.; Kitayama, Shinobu; Karasawa, Mayumi; Markus, Hazel; Kawakami, Norito; Coe, Christopher
In 2008, with funding from the National Institute on Aging (NIA), baseline survey data for the Survey of Midlife in Japan (MIDJA), April-September 2008 were collected from a probability sample of Japanese adults (N=1,027) aged 30 to 79 from the Tokyo metropolitan area (ICPSR 30822). In 2009-2010 biomarker data was obtained from a subset of these cases (ICPSR 34969).
The survey and biomarker measures obtained parallel those in a national longitudinal sample of Americans known as Midlife in the United States or MIDUS (ICPSR 2760: MIDUS 1 and ICPSR 4652: MIDUS 2). The central objective was to compare the Japanese sample (MIDJA) with the United States sample (MIDUS) to test hypotheses about the role of psychosocial factors in the health (broadly defined) of mid- and later-life adults in Japan and the United States.
In 2012, with additional support from NIA, a longitudinal follow-up of the MIDJA sample was completed. The data collection for this second wave (N=657) largely repeated the baseline assessments. The goal of the follow-up wave was to conduct comparisons of longitudinal data available from the Japanese sample (MIDJA) and the United States sample (MIDUS) to test the hypothesis about the role of psychosocial factors in predicting health changes (including biomarkers) in both cultural contexts. Cultural influences on age differences in health and well-being were also of interest.
Demographic and background information included gender, age, education, marital status, household composition, and income.
2018-02-19
42.
UC Berkeley Social Networks Study (UCNets), San Francisco Bay Area, 2015-2018 (ICPSR 36975)
Fischer, Claude S.
Fischer, Claude S.
Understanding How Personal Networks Change: Wave 1 (UCNets) is the University of California Berkeley Social Networks Study, a longitudinal study with the objective of understanding how network composition changes over time as a result of life course transitions - e.g., graduation, marriage, retirement or widowhood - and how these changes are related to health status and outcomes. Using mostly addressed-based sampling from six San Francisco Bay Area counties, the study recruited participants in two age groups (cohorts) - 21-30 year-olds and 50-70 year-olds -- to maximize the possibility of experiencing a life transition. There are 3 waves of interviewing. The first interview, Wave 1, was May 2015 through January 2016. The re-interview
for Wave 2 was conducted in Feb-June 2017, and Wave 3 was during Feb-May 2018. In Wave 1, the majority of respondents completed a face-to-face (FTF) survey, with the rest filling out a comparable web survey. In Wave 2 about half completed the FTF survey, and in Wave 3, about one-quarter. The survey contains items regarding households, personal networks, family milestones, employment, health status and behavior, personality and demographic characteristics.
2020-07-22
43.
The Victim-Offender Overlap: Examining Police and Service System Networks of Response Among Violent Street Conflicts, Philadelphia, Pennsylvania, 2018-2019 (ICPSR 37601)
Roman, Caterina Gouvis
Roman, Caterina Gouvis
The study examined the networks of service delivery around violent assaults involving street conflicts and disputes. The research was designed to expand understanding of the situational and contextual factors around street violence that impact how individuals who have past justice system involvement access (or do not access) victim services after being violently injured. The project used a mixed-method design that yielded both qualitative and quantitative data. Qualitative data were drawn from focus groups, semi-structured interview with victim services providers, and in-depth interviews with 103 victims of street crime. Quantitative data were drawn from surveys and social network data collection with those same 103 victims of violent street assaults.
2024-06-26