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National Congregations Study: Cumulative File, 1998, 2006-2007, 2012, 2018-2019, [United States] (ICPSR 3471)

Released/updated on: 2025-06-03
Geographic coverage: United States
Time period: 1998-01-01--1998-12-31, 2006-01-01--2006-12-31, 2012-01-01--2012-12-31, 2018-01-01--2019-12-31

The National Congregations Study (NCS) is a national survey effort to gather information about America's congregations. The first wave of the NCS took place in 1998, and the study was repeated in 2006-07, 2012, and 2018-19. The NCS tracks continuity and change among American congregations, and each NCS wave also explores new subjects.

With information from 5,333 congregations collected over a span of more than 20 years, the NCS helps us better understand many aspects of congregational life in the United States, and how congregations are changing in the 21st century. The NCS contributes to knowledge about American religion by collecting information about a wide range of congregations' characteristics and activities at different points in time.

In all four waves, the NCS was conducted in conjunction with the General Social Survey (GSS). The 1998, 2006, 2012, and 2018 waves of the GSS asked respondents who attend religious services to name their congregation, thus generating a nationally representative sample of religious congregations. Researchers then located these congregations. In 2006, the sample included re-interviews of a subset of congregations that participated in 1998, and in 2018-19, the sample included re-interviews of a subset of congregations that participated in 2012.

A key informant at each congregation - a minister, priest, rabbi, or other staff person or leader - provided each congregation's information via a one-hour interview conducted either over the phone or in-person. The survey gathered information on many topics, including the congregation's leadership, social composition, structure, activities, and programming. The NCS gathers information about worship, programs, staffing, community activities, demographics, funding, and many other characteristics of American congregations. Respondents of the NCS survey were asked to describe the worship service and programs sponsored by the congregation other than the main worship services, including religious education classes, musical groups, and recreational programs. Informants described the type of building in which the congregation met, whether it belonged to the congregation, and whether visitors came just to view the building's architecture or artwork. Congregations were geocoded, and selected census variables are included in this study.

Curated

Costing Study of the Clients of the Mobile Community Treatment Program [1987-1988: Madison, Wisconsin] (ICPSR 9843)

Released/updated on: 2024-02-14
Geographic coverage: Madison, United States, Wisconsin
Time period: 1987-01-01--1988-12-31
The University of Wisconsin's Department of Preventive Medicine, in cooperation with the Department of Psychiatry and the Mental Health Center of Dane County, Wisconsin, conducted a comprehensive costing study of the clients of a community-based program for treating the mentally ill, the Mobile Community Treatment program (MCT), in Madison, Wisconsin. MCT provided assertive outreach and case management for individuals with major psychiatric disorders. The aim of this study was to determine the costs for clients of MCT to live in the community, including the costs of their medical, residential, employment, law enforcement, and maintenance needs. Clients of MCT were queried about their use of services provided by medical, human service, and law enforcement agencies, as well as their receipt of in-kind and cash benefits from public and private agencies. Service and cost data on survey respondents were also obtained from the records of local agencies, such as the Dane County Sheriff's Department, Dane County Circuit Court, Dane County Department of Public Health, homeless shelters, Adult Protective Services, and vocational training programs.
Self-published

2010 Survey of U.S. Publicly Funded Family Planning Clinics (ICPSR 163961)

Released/updated on: 2022-03-31
Geographic coverage: United States
Time period: 2010-01-01--2011-12-31
The Guttmacher Institute has a long history of studying U.S. publicly funded family planning clinics and conducting sample surveys to better understand and document the clinic network’s range of service delivery practices and the challenges it faces. These data are from a survey of a nationally representative sample of publicly funded family planning clinics conducted in 2010–2011 and are both an extension of earlier surveys and an investigation of new topic areas relevant to the provision of clinic services today. A total of 664 publicly funded family planning clinics in the U.S. provided information about the types of contraceptive methods and related services offered onsite and through referral; service delivery practices and protocols, particularly those that have the potential to affect service accessibility, method initiation and continuation, and care for patients with special needs; the types of outreach and special programs offered; protocols and technology used for screening and testing (including for cervical cancer and HIV); services for male partners and clients; service costs and financial challenges; and a variety of other aspects related to clinical practices and management.
Curated
Restricted

Evaluation of CeaseFire, a Chicago-based Violence Prevention Program, 1991-2007 (ICPSR 23880)

Released/updated on: 2015-02-25
Geographic coverage: United States, Chicago, Illinois
Time period: 1991-01-01--2006-12-31, 1998-02-01--2006-04-30, 2006-05-01--2007-08-31, 2006-09-01--2007-02-28, 2007-04-05--2007-07-19

This study evaluated CeaseFire, a program of the Chicago Project for Violence Prevention. The evaluation had both outcome and process components.

The outcome evaluation assessed the program's impact on shootings and killings in selected CeaseFire sites. Two types of crime data were compiled by the research team: Time Series Data (Dataset 1) and Shooting Incident Data (Dataset 2). Dataset 1 is comprised of aggregate month/year data on all shooting, gun murder, and persons shot incidents reported to Chicago police for CeaseFire's target beats and matched sets of comparison beats between January 1991 and December 2006, resulting in 1,332 observations. Dataset 2 consists of data on 4,828 shootings that were reported in CeaseFire's targeted police beats and in a matched set of comparison beats for two-year periods before and after the implementation of the program (February 1998 to April 2006).

The process evaluation involved assessing the program's operations and effectiveness. Researchers surveyed three groups of CeaseFire program stakeholders: employees, representatives of collaborating organizations, and clients.

The three sets of employee survey data examine such topics as their level of involvement with clients and CeaseFire activities, their assessments of their clients' problems, and their satisfaction with training and management practices. A total of 154 employees were surveyed: 23 outreach supervisors (Dataset 3), 78 outreach workers (Dataset 4), and 53 violence interrupters (Dataset 5).

The six sets of collaborating organization representatives data examine such topics as their level of familiarity and contact with the CeaseFire program, their opinions of CeaseFire clients, and their assessments of the costs and benefits of being involved with CeaseFire. A total of 230 representatives were surveyed: 20 business representatives (Dataset 6), 45 clergy representatives (Dataset 7), 26 community representatives (Dataset 8), 35 police representatives (Dataset 9), 36 school representatives (Dataset 10), and 68 service organization representatives (Dataset 11).

The Client Survey Data (Dataset 12) examine such topics as clients' involvement in the CeaseFire program, their satisfaction with aspects of life, and their opinions regarding the role of guns in neighborhood life. A total of 297 clients were interviewed.

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The Effectiveness of Coordinated Outreach in Intimate Partner Violence Cases in Denver, Colorado 2007 to 2009 (ICPSR 30961)

Released/updated on: 2014-11-07
Geographic coverage: United States, Colorado, Denver
Time period: 2007-01-01--2009-12-31

In collaboration with community- and system-based partners, the current study used an experimental design to test the impact of phone outreach from community-based agencies to women exposed to Intimate Partner Violence (IPV) compared to phone referrals provided by system-based unit (i.e., the Victim Assistance Unit of the DPD or the City Attorney's Office) in a racially and ethnically diverse sample of women whose cases have come to the attention of the criminal justice system. The phone outreach was informed by an interdisciplinary team involving both system- and community-based team members. Participants, who were randomly selected to receive outreach or treatment-as-usual, were interviewed at three time points: after an incident of IPV was reported to the police (T1), 6 months after T1, and 12 months after T1. The study addressed three primary roles. First, investigators evaluated the effectiveness of a coordinated, community-based outreach program in improving criminal justice and victim safety and empowerment outcomes for IPV victims using a longitudinal, randomized control design. Second, victim and case characteristics that moderated outcomes were identified. Third, the influence of spatial characteristics on criminal justice outcomes was evaluated.

Curated
Restricted

Strategic Prevention Framework State Incentive Grant (SPF SIG) National Cross-Site Evaluation [Restricted Use] (ICPSR 28921)

Released/updated on: 2014-03-24
Geographic coverage: North Carolina, Vermont, Indiana, United States, Wyoming, Tennessee, Maine, Arkansas, Washington, West Virginia, Colorado, Missouri, Guam, Arizona, Nevada, Rhode Island, Montana, Kentucky, Florida, Michigan, New Mexico, Illinois, Texas, Connecticut, New Hampshire, Louisiana, Palau
Time period: 2005-08-01--2007-09-30, 2006-12-14--2007-08-14, 2008-09-15--2009-06-30, 2008-10-15--2009-06-15, 2006-07-01--2006-09-30, 2005-12-01--2007-12-31, 2008-01-01--2008-06-30, 2008-07-01--2008-12-31, 2009-01-01--2009-06-30, 2009-07-01--2009-12-31, 2010-01-01--2010-06-30, 2005-12-01--2007-12-31, 2008-01-01--2008-06-30, 2008-07-01--2008-12-31, 2009-01-01--2009-06-30, 2009-07-01--2009-12-31, 2010-01-01--2010-06-30, 2005-12-01--2007-12-31, 2008-01-01--2008-06-30, 2008-07-01--2008-12-31, 2009-01-01--2009-06-30, 2009-07-01--2009-12-31, 2010-01-01--2010-06-30
The Strategic Prevention Framework State Incentive Grant (SPF SIG) National Cross-Site Evaluation was conducted to evaluate the Center for Substance Abuse Prevention (CSAP)'s SPF SIG initiative, which sought to: (1) prevent the onset and reduce the progression of substance abuse, including childhood and underage drinking; (2) reduce substance abuse-related problems in communities; and (3) build prevention capacity and infrastructure at the state and community levels. This cross-site evaluation included the 21 states and territories CSAP funded in FY2004 (Cohort 1) and an additional 5 States funded in Cohort 2 in FY2005 that were funded for up to 5 years to implement the SPF. The SPF is a five-step prevention planning model that requires states to: (1) conduct a statewide needs assessment, including the establishment of a State Epidemiological and Outcomes Workgroup (SEOW); (2) mobilize and build state and community capacity to address needs; (3) develop a statewide strategic plan for prevention; (4) implement evidence-based prevention, policies, and practices (EBPPP) to meet state and community needs; and (5) monitor and evaluate the implementation of their SPF SIG project. Under contract to the Substance Abuse and Mental Health Services Administration (SAMHSA) with funding provided by the National Institute on Drug Abuse (NIDA), Westat, in collaboration with the Pacific Institute for Research and Evaluation (PIRE) and The MayaTech Corporation, implemented a multilevel, multi-method quasi-experimental design to evaluate SPF SIG's impact. The scope of the evaluation encompassed national, state, and community levels. The design included comparison conditions at both the state and community levels. These data represent Phase I of the restricted use data release and contains extensive data on state-level implementation, community-level implementation, and state-level infrastructure, as well as other reference elements. A subsequent release (Phase II) will include state- and community-level outcomes, as well as data on community-level implementation, community-level implementation fidelity, state-level sustainability, and mediating variables.
Curated
Restricted

Chicago Male Drug Use and Health Survey (MSM Supplement), 2002-2003 (ICPSR 34303)

Released/updated on: 2012-08-01
Geographic coverage: United States, Chicago, Illinois
Time period: 2002-09-01--2003-01-31
In recent years, club drugs such as MDMA, Ketamine, GHB, and Rohypnol have emerged as major drugs of abuse. The national and local Chicago news media have publicized law enforcement actions and adverse health outcomes, including fatalities, related to the abuse of these substances. Media accounts and a limited body of research have identified use of these substances as prevalent in the gay male community. This prevalence coincides with recent increases in HIV seropositive incidence. There is a clear need for a more comprehensive understanding of the prevalence of club drug use in the general population, and particularly in the subgroup of sexually active gay men. Noting these research gaps and their considerable adverse public health implications, this supplemental study was designed to apply an expanded protocol developed from an earlier study conducted (Feasibility and Use of Biological Measurement in Drug Surveys; R01DA12425, SRL Study #860) to a sample of gay men in the city of Chicago (Michael Fendrich, Principal Investigator). This study evaluated whether findings regarding the feasibility and use of drug testing in drug surveys derived from general population samples are generalizable to a probability sample of 216 gay men in the city of Chicago. For this project, a supplemental module was added to the main study survey that asked detailed questions about involvement in the gay community, risky sexual activity and HIV seropositivity. The scope of biological measurement was also expanded to incorporate testing for Rohypnol and Ketamine in hair (MDMA was already being tested as part of the general sample hair screen). The dataset contains 676 variables.
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Restricted

Evaluation of the Healthy Families New York Home Visiting Program, Age Seven Follow Up, 2007-2009 (ICPSR 30441)

Released/updated on: 2012-04-27
Geographic coverage: United States, New York (state)
Time period: 2000-01-01--2009-12-31

Healthy Families New York (HFNY), which was based on the Healthy Families America (HFA) model, was established as a strengths-based, intensive home visitation program with the explicit goals of promoting positive parenting skills and parent-child interaction; preventing child abuse and neglect; supporting optimal prenatal care, and child health and development; and improving parent's self-sufficiency.

In 2000, a randomized controlled trial was initiated at three sites with the HFNY home visiting program. Families eligible for HFNY at each site were randomly assigned to either an intervention group that was offered HFNY services or to a control group that was given information on and referral to appropriate services other than home visiting. Baseline interviews were conducted with 1,173 of the eligible women (intervention, n=579; control, n=594), and follow up interviews at Years 1, 2, and 3. In addition to data gathered during the follow up interviews, information regarding study participants' involvement in reports of child maltreatment was also extracted and coded from Child Protection Services records.

For the current study, mothers in both the intervention and control groups were re-interviewed at the time of the target child's seventh birthday. Interviews (Dataset 1: Mother Interview Data, n=942) included information about parenting, the child, earnings, and household composition. Interviewers also completed face-to-face assessments (Dataset 2: Target Child Interview Data) with 800 of the children who were born and reached the age of 7 at the time of interview. The target child interviews assessed children's receptive vocabulary skills, emotional health, self-regulatory abilities, and problem behaviors. The research team also extracted or obtained administrative data pertaining to Child Protective Service reports, foster care placements, federal and state supported benefits, and programs services and costs (Datasets 3-8).

Curated

Cooperative Agreement for AIDS Community-Based Outreach/Intervention Research Program, 1992-1998: [United States] (ICPSR 3023)

Released/updated on: 2008-10-23
Geographic coverage: United States
Time period: 1992-01-01--1998-12-31
The purpose of the Cooperative Agreement (CA) Research Program was to monitor risk factors, risk behaviors, and rates of HIV seroprevalence and seroincidence among out-of-treatment, multi-ethnic/racial injection drug users and crack cocaine users. The program evaluated the efficacy of experimental interventions designed to prevent, eliminate, or reduce HIV risk behaviors and developed new treatment interventions. All participants received the standard intervention, which consisted of street-based outreach and HIV prevention counseling. Those assigned to enhanced interventions received more counseling sessions, educational videos, social gatherings, and support group activities. The public-use data file contains 31,088 respondent records, collected from 21 CA program facilities in the United States and one facility each in Puerto Rico and Brazil. Hence, the process data file contains 23 records of facility information that can be linked to individual respondents. Respondent interviews include a baseline Risk Behavior Assessment (completed prior to first intervention) and a Follow-Up Assessment, conducted either three months or six months after the baseline survey. Respondent data were augmented with eligibility information, biological markers of drug use, HIV test results, and intervention assignment. At baseline and post-intervention, the surveys measured drug use and drug treatment, sexual activity and sex for money/drugs, arrests, work/income, HIV/STD/pregnancy status, perceptions of risk, and risk reduction behaviors. The process questionnaires were completed by staff or principal investigators at the 23 site locations. Process data describe the program structure and process, other intervention projects in the community, needle exchange programs and pharmacy syringe sales, and local HIV infection rates. Drugs reported on include alcohol, marijuana/hashish, crack/cocaine, heroin (including speedball), non-prescription methadone, other opiates, and amphetamines.
Curated

Resources for Enhancing Alzheimer's Caregiver Health (REACH II), 2001-2004 (ICPSR 4354)

Released/updated on: 2006-10-27
Geographic coverage: Palo Alto, United States, Tennessee, Memphis, California, Alabama, Florida, Birmingham, Philadelphia, Pennsylvania, Miami
Time period: 2001-01-01--2004-12-31
Built upon the findings of RESOURCES FOR ENHANCING ALZHEIMER'S CAREGIVER HEALTH, 1996-2001, BASELINE AND FOLLOW-UP DATA [ICPSR 3678], REACH II designed and tested a single multi-component intervention among family caregivers of persons with Alzheimer's disease or related disorders. The overall objectives were (1) to identify and reduce modifiable risk factors among diverse family caregivers of patients with Alzheimer's Disease or a related disorder, (2) to enhance the quality of care provided to the care recipients, and (3) to enhance the well-being of the caregivers. REACH II is the first project to simultaneously test a comprehensive caregiver intervention in three distinct racial/ethnic groups: Hispanic/Latino, Black/African-American, and White/Caucasian. The intervention was based on a risk-appraisal approach in which five areas of risk--depression, burden, self-care, social support, and patient problem behaviors--that are central to caregiver well-being and quality of life were matched to corresponding intervention components. These components included education, skills to manage troublesome care-recipient behaviors, social support, cognitive strategies for reframing negative emotional responses, and strategies for enhancing healthy behaviors and managing stress. Consistent with this approach, the primary outcome was a multivariate quality of life indicator that assessed caregiver depression, burden, self-care, social support, and patient problem behaviors. Two hallmarks of caregiver intervention studies--caregiver clinical depression and patient institutionalization--were assessed as secondary outcomes. The dataset names listed in this collection include the shortened name of the form administered.
Curated

Resources for Enhancing Alzheimer's Caregiver Health, 1996-2001, Baseline and Follow-Up Data (ICPSR 3678)

Released/updated on: 2006-09-26
Geographic coverage: United States, Tennessee, California, Alabama, Florida, Birmingham, Pennsylvania, Miami, Palo Alto, Massachusetts, Memphis, Philadelphia, Boston
Time period: 1996-09-01--2001-02-28
Resources for Enhancing Alzheimer's Caregiver Health (REACH) was established in 1995 to conduct social and behavioral research on interventions designed to enhance family caregiving, particularly in minority families, for persons with Alzheimer's Disease and related disorders. Baseline data (ICPSR 3253) were collected through randomized clinical trials at six sites: University of Alabama-Birmingham, The Research and Training Institute of the Hebrew Rehabilitation Center for Aged in Boston, University of Tennessee-Memphis, University of Miami, Veterans Affairs Palo Alto Health Care System and Stanford University, and Thomas Jefferson University in Philadelphia. Interventions such as psychoeducational support groups, behavioral skills training programs, family-based systems interventions, environmental modifications, and technological computer-based information and communication services varied by site. This collection contains baseline data along with follow-up data at 6-, 12-, and 18-month intervals from each site with focus on the impact of the various intervention strategies on psychological distress, health status, health practices, and health care utilization. Also included are follow-up batteries, transition batteries (placement, bereavement, discontinued), and data reporting missed visits. Parts 1 through 5 contain screening data and responses to a short mental status questionnaire. Parts 6 through 34 contain baseline data along with follow-up data at 6, 12, and 18-month intervals and cover activities of daily living, anxiety, and caregiver health and health behaviors along with sociodemographic information. Also included are care recipient medications and sociodemographic information. Parts 35 through 40 contain tracking data and also include an examination of interventions.
Curated

Resources for Enhancing Alzheimer's Caregiver Health, 1996-2001 (ICPSR 3253)

Released/updated on: 2006-03-30
Geographic coverage: United States, Tennessee, California, Alabama, Florida, Birmingham, Pennsylvania, Miami, Palo Alto, Massachusetts, Memphis, Philadelphia, Boston
Time period: 1996-09-01--2001-02-28
Resources for Enhancing Alzheimer's Caregiver Health (REACH) was established in 1995 to conduct social and behavioral research on interventions designed to enhance family caregiving, particularly in minority families, for persons with Alzheimer's Disease and related disorders. Data were collected through randomized clinical trials at six sites: University of Alabama--Birmingham, the Research and Training Institute of the Hebrew Rehabilitation Center for Aged in Boston, University of Tennessee--Memphis, University of Miami, Veterans Affairs Palo Alto Health Care System and Stanford University, and Thomas Jefferson University in Philadelphia. Interventions studied included psychoeducational support groups, behavioral skills training programs, family-based systems interventions, environmental modifications, and technological computer-based information and communication services. Although interventions varied by site, all sites collected the same data at the same time intervals. The impact of the various intervention strategies on psychological distress, health status, health practices, and health care utilization was assessed. Parts 1 through 5 contain screening data and a short mental status questionnaire. Parts 6 through 24 contain baseline data and cover activities of daily living, anxiety, and caregiver health and behaviors along with sociodemographic information. Also included are care recipient medications and sociodemographic information. Parts 25 and 26 contain tracking data and also include an examination of interventions.
Curated

Law-Related Education Evaluation Project [United States], 1979-1984 (ICPSR 8406)

Released/updated on: 2006-01-18
Geographic coverage: United States
Time period: 1979-01-01--1984-12-31
This data collection contains information gathered to evaluate certain activities of a number of organizations dedicated to the advancement of law-related education (LRE) in elementary, junior high, and senior high schools. The organizations whose activities were evaluated were (1) the Constitution Rights Foundation, (2) Law in a Free Society, (3) the National Street Law Institute, (4) the American Bar Association's Special Committee on Youth Education for Citizenship, (5) the Children's Legal Rights Information and Training Program, and (6) the Phi Alpha Delta Committee for Juvenile Justice. The evaluation research dealt primarily with two types of issues: (1) the degree of increase in awareness of and receptivity toward LRE among the nation's educators, juvenile justice, and other related professionals, as well as the degree of institutionalization of LRE in certain targeted states (i.e., California, Michigan, and North Carolina), and (2) the degree to which LRE could produce changes in students' knowledge of and attitudes about the law, and reduce juvenile delinquency (measured both by self-reported delinquency rates and by attitudes previously shown to be correlated with delinquent behavior). In 1981 (Part 1) and again in 1982 (Part 2), questionnaires were mailed to a sample of professionals in state educational organizations as well as to elementary and secondary school principals, juvenile justice specialists, juvenile and family court judges, police chiefs, and law school deans. Respondents were asked whether they had heard of the various projects, what they thought of LRE in terms of its impact on students and usefulness in the curriculum, whether LRE should be required, what type of publicity had contributed to their awareness of LRE, and the degree of involvement they would be willing to have in promoting or developing LRE programs. In a second component of the study, primary and secondary school students were selected for an impact evaluation of the LRE activities run by the six organizations under evaluation. Questionnaires were administered to students during academic years 1982-1983 (Part 3) and 1983-1984 (Part 4), before and after participating in LRE courses offered by the programs under evaluation. Control students (not taking LRE courses) were also used for the comparisons. The questionnaires tested the knowledge, attitudes (measuring such factors as isolation from school, delinquent peer influence, negative labeling, and attitudes toward violence), and self-reported delinquency of school children. Demographic information collected about the student respondents includes sex, age, race, grade in school, and grade-point average.
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