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Showing 1 – 9 of 9 results.
Curated

CDC WONDER (ICPSR 128)

Released/updated on: 2006-03-08
Geographic coverage: United States
CDC WONDER is the online public information health system created by the Centers for Disease Control and Prevention (CDC). It provides a single point of access to a wide variety of CDC reports, guidelines, and numeric public health data. With it, one can search for and retrieve MMWR (Morbidity and Mortality Weekly Report) articles and Prevention Guidelines published by the CDC, as well as query dozens of numeric datasets on CDC's mainframe and other computers via "fill-in-the blank" request screens. Public-use datasets about mortality, cancer incidence, hospital discharges, AIDS, behavioral risk factors, diabetes, and many other topics are available for query, and the requested data can be readily summarized and analyzed.
Curated

Criminal Justice Drug Abuse Treatment Studies (CJ-DATS): HIV/HEPATITIS Prevention for Re-Entering Drug Offenders (ICPSR 29061)

Released/updated on: 2011-01-24
Geographic coverage: United States, Delaware
The development of the CJ-DATS Targeted Intervention program, targeting a policy change to incorporate public health concerns into the parole and release process, has prompted this study to analyze the effectiveness of the intervention and to determine how it might best be integrated into the current corrections administration. Primarily, the study seeks to consider the effectiveness of one-on-one peer intervention against group intervention moderated by a peer. The study is set up to interview former inmates as they re-enter society through parole or work release. The first phase of the study is to determine their history of drug use, before incarceration and during their time in a corrections facility. These respondents were chosen because of the particular danger faced by those re-entering to engage in "make up for lost time" behavior as access to illicit activity becomes more readily available. Additionally, this portion tests the respondents' knowledge of HIV/AIDS and their utilization of resources designed to improve their health. Following this survey, as well as a blood examination to determine whether they have the illnesses associated with the study, the subjects engaged in counseling based on the subgroup to which they had been randomly assigned. The control group received a standard one-hour, non-interactive CDC intervention, while the experimental group received the CJ-DATS Targeted Intervention. The intention was to determine if individual intervention is more effective, given the need for brief, effective interventions as a result of the large volume of the relevant population. Following the interventions, followup interviews were issued at 30 and 90 days. The intention was to determine not merely if there was an aggregate change in behavior as a result of the intervention, but furthermore, if the intervention led to a negative trend. Of particular concern to the outcome of the study and its analysis was the relative effectiveness of the peer interventions, as well as how officers and administration within the corrections and parole process might incorporate an attitude of public health into the process.
Curated

Health Information National Trends Survey (HINTS), 2003 (ICPSR 24382)

Released/updated on: 2009-03-27
Geographic coverage: United States
The Health Information National Trends Survey (HINTS) collects nationally representative data about the American public's access to and use of cancer-related information. This data collection consists of the 2003 survey which focused on the changing patterns, needs, and behavior in seeking and supplying cancer information, and explored how cancer risks are perceived. A series of questions specifically addressed colon and breast cancer and respondents' familiarity with cancer screening procedures such as mammogram, colonoscopy, and the PSA test. Information was also gathered on physical and mental health status, smoking history, how often respondents ate fruits and vegetables, and whether they had health insurance. Demographic variables include sex, age, race, education level, employment status, marital status, household income, type of residential area (e.g., urban or rural), and whether respondents had children under the age of 18.
Curated

Health Information National Trends Survey (HINTS), 2005 (ICPSR 24383)

Released/updated on: 2009-04-13
Geographic coverage: United States
The Health Information National Trends Survey (HINTS) collects nationally representative data about the American public's access to and use of cancer-related information. The 2005 HINTS survey is the second in an ongoing biannual series and provided information on the changing patterns, needs, and behavior in seeking and supplying cancer information, and explored how cancer risks are perceived. A series of questions addressed colon, lung, cervical, and breast cancer, the Human Papillomavirus (HPV), and respondents' familiarity with cancer screening procedures such as mammogram, colonoscopy, and the PSA test. Specific questions were also posed about the relationship between cancer, diet, and exercise. Information was also gathered on physical and mental health status, participation in community organizations, smoking history, how often respondents ate fruits and vegetables, and whether they had health insurance. Demographic variables include sex, age, race, education level, employment status, marital status, household income, frequency of religious attendance, number of people in the household, ownership of residence, type of residential area (e.g., urban or rural), and whether respondents were born in the United States.
Curated

Health Information National Trends Survey (HINTS), 2007 (ICPSR 25262)

Released/updated on: 2009-06-23
Geographic coverage: United States
The Health Information National Trends Survey (HINTS) collects nationally representative data about the American public's access to and use of cancer-related information. The 2007 HINTS survey is the third in an ongoing biannual series and provides information on the changing patterns, needs, and behavior in seeking and supplying cancer information and explores how cancer risks are perceived. Respondents were asked about the ways in which they obtained health information, their use of health care services, their views about medical information and research, and their beliefs about cancer. A series of questions specifically addressed cervical cancer, colon cancer, and the Human Papillomavirus (HPV). Information was also collected on physical and mental health status, diet, physical activity, sun exposure, history of cancer, tobacco use, and whether respondents had health insurance. Demographic variables include sex, age, race, education level, employment status, marital status, household income, number of people living in the household, ownership of residence, and whether respondents were born in the United States.
Curated
Partially restricted
Simple Crosstabs

Latino MSM Community Involvement: HIV Protective Effects (ICPSR 34385)

Released/updated on: 2014-04-02
Geographic coverage: San Francisco, United States, Chicago, Illinois, California
The purpose of this study was to contribute to the conceptual understanding and practical application of social integration theory to health behaviors. The research aimed to investigate the protective effects of community involvement in HIV/AIDS and gay-related organizations for HIV/AIDS sexual risk behavior among Latino gay or bisexual men and transgender individuals in Chicago and San Francisco. As part of this, the study examined HIV prevalence and the socioeconomic correlates of HIV infection, sexual risk behaviors, and substance use. Further, the study tested whether community involvement in AIDS and LGBT organizations moderated the relationship of racial and homosexual stigma to sexual risk behavior. Data were collected from a sample of 643 individuals (Chicago: n=320; San Francisco: n=323) through respondent-driven sampling and computer-assisted self-administered interviews. Demographic variables included ethnic identification, sexual identification, ZIP code (only available in restricted use data), country of birth, years in the United States, employment status, income, family religion, age, and health/STD status.
Curated
Simple Crosstabs

Midlife in the United States (MIDUS 2): Biomarker Project, 2004-2009 (ICPSR 29282)

Released/updated on: 2025-06-18
Geographic coverage: United States
Time period: 2004-07-30--2009-05-31

The Biomarker study is Project 4 of the Midlife in the United States (MIDUS) longitudinal study, a national survey of more than 7,000 Americans (aged 25 to 74) begun in 1994. The purpose of the larger study was to investigate the role of behavioral, psychological, and social factors in understanding age-related differences in physical and mental health. With support from the National Institute on Aging (NIA), a longitudinal follow-up of the original MIDUS samples [core sample (N = 3,487), metropolitan over-samples (N = 757), twins (N = 957 pairs), and siblings (N = 950)] was conducted in 2004-2006. Guiding hypotheses, at the most general level, were that behavioral and psychosocial factors are consequential for health (physical and mental). A description of the study and findings from it are available on the MIDUS website.

The Biomarker Project (Project 4) of MIDUS 2 contains data from 1,255 respondents. These respondents include two distinct subsamples, all of whom completed the Project 1 Survey: (1) longitudinal survey sample (n = 1,054) and (2) Milwaukee sample (n = 201). The Milwaukee group contained individuals who participated in the baseline MIDUS Milwaukee study, initiated in 2005. The purpose of the Biomarker Project (Project 4) was to add comprehensive biological assessments on a subsample of MIDUS respondents, thus facilitating analyses that integrate behavioral and psychosocial factors with biology. The broad aim is to identify biopsychosocial pathways that contribute to diverse health outcomes. A further theme is to investigate protective roles that behavioral and psychosocial factors have in delaying morbidity and mortality, or in fostering resilience and recovery from health challenges once they occur. The research was not disease-specific, given that psychosocial factors have relevance across multiple health endpoints.

Biomarker data collection was carried out at three General Clinical Research Centers (at UCLA, University of Wisconsin, and Georgetown University). The biomarkers reflect functioning of the hypothalamic-pituitary-adrenal axis, the autonomic nervous system, the immune system, cardiovascular system, musculoskeletal system, antioxidants, and metabolic processes. Our specimens (fasting blood draw, 12-hour urine, saliva) allow for assessment of multiple indicators within these major systems. The protocol also included assessments by clinicians or trained staff, including vital signs, morphology, functional capacities, bone densitometry, medication usage, and a physical exam. Project staff obtained indicators of heart-rate variability, beat to beat blood pressure, respiration, and salivary cortisol assessments during an experimental protocol that included both a cognitive and orthostatic challenge. Finally, to augment the self-reported data collected in Project 1, participants completed a medical history, self-administered questionnaire, and self-reported sleep assessments. For respondents at one site (UW-Madison), objective sleep assessments were also obtained with an Actiwatch(R) activity monitor.

Curated
Simple Crosstabs

Midlife in the United States (MIDUS Refresher 1): Biomarker Project, 2012-2016 (ICPSR 36901)

Released/updated on: 2019-11-18
Geographic coverage: United States
Time period: 2012-10-01--2016-08-01

The MIDUS Refresher study Survey (2011-2014 ICPSR 36532) recruited a national probability sample of 3,577 adults, aged 25 to 74, designed to replenish the original MIDUS 1 baseline cohort and paralleling the five decadal age groups of the MIDUS 1 baseline survey (ICPSR 2760). The MIDUS Refresher survey employed the same comprehensive assessments as those assembled on the core longitudinal MIDUS sample, but with additional questions about impacts of the economic recession of 2008-09. The MIDUS Refresher Biomarker study (2012-2016) obtained data from 863 respondents (n=746 Main sample, n=117 African Americans from Milwaukee) who completed the MIDUS Refresher Survey.

The purpose of the Refresher Biomarker Project (Project 4) parallels that of the MIDUS 2 Biomarker project (ICPSR 29282), which collected comprehensive biological assessments on a subsample of MIDUS respondents, thus facilitating analyses that integrate behavioral and psychosocial factors with biological regulation/dysregulation, broadly defined. The aim was to use such data to explicate biopsychosocial pathways that contributed to diverse health outcomes. A further theme was to examine period effects on health (mental and physical) related to the economic recession by comparing the pre-recession MIDUS sample with the post-recession MIDUS Refresher sample. A further objective of the MIDUS Refresher sample was to strengthen cross-project analyses by increasing the sample sizes available for testing hypotheses regarding the interplay of key factors (e.g., socioeconomic status, gender, psychosocial factors, biological factors) in mid- and later-life health.

Biomarker data collection was carried out at hypothalamic-pituitary-adrenal axis, the autonomic nervous system, the immune system, cardiovascular system, musculoskeletal system, antioxidants, and three General Clinical Research Centers (at UCLA, University of Wisconsin, and Georgetown University). The biomarkers reflect functioning of the metabolic processes. Our specimens (fasting blood draw, 12-hour urine, saliva) allowed for assessment of multiple indicators within these major systems. The protocol also included assessments by clinicians or trained staff, including vital signs, morphology, functional capacities including 3 dimensional gait analysis, bone densitometry, body composition, ankle brachial index, medication usage, and a physical exam. Project staff obtained indicators of heart-rate variability, beat to beat blood pressure, respiration, and salivary cortisol assessments during an experimental protocol that included both a cognitive and orthostatic challenge. Finally, to augment the self-reported data collected in Survey (Project 1), participants completed a medical history, self-administered questionnaire, and self-reported sleep assessments. For respondents at one site (UW-Madison), objective sleep assessments were also obtained with an Actiwatch(R) activity monitor.

Curated

National Health Interview Survey, 1987: AIDS Supplement (ICPSR 9271)

Released/updated on: 1992-02-17
Geographic coverage: United States
The basic purpose of the Health Interview Survey (HIS) is to obtain information about the amount and distribution of illness, its effects in terms of disability and chronic impairments, and the kinds of health services people receive. Person variables include sex, age, race, marital status, veteran status, education, income, industry and occupation codes, and limits on activity. This AIDS Supplement also features information on knowledge of and attitudes towards the disease. Variables include questions on the effects of the disease, how AIDS is spread, where to obtain information on AIDS, blood tests for AIDS, how to avoid getting the disease, and personal knowledge of anyone who had the test for AIDS or had the virus or AIDS disease.