I C P S R

National Institute on Aging

Description & Citation--Study No. 4354

Bibliographic Description

ICPSR Study No.:4354
 
Persistent URL: http://dx.doi.org/10.3886/ICPSR04354
 
Title:Resources for Enhancing Alzheimer's Caregiver Health (REACH II), 2001-2004
 
Alternate Title:REACH II, 2001-2004
 
Principal Investigator(s):Richard Schulz, University of Pittsburgh. University Center for Social and Urban Research
 
  Louis Burgio, University of Alabama. Applied Gerontology Program
 
  Alan B. Stevens, Texas A&M University. Health Science Center. College of Medicine
 
  Robert Burns, Memphis Veterans Affairs Medical Center
 
  Sara Czaja, University of Miami. Miller School of Medicine. Center on Aging
 
  Dolores Gallagher Thompson, Stanford University. Stanford School of Medicine. Department of Psychiatry and Behavioral Sciences
 
  Laura N. Gitlin, Thomas Jefferson University. School of Health Professions. Center for Applied Research on Aging and Health
 
  Steven Belle, University of Pittsburgh. Graduate School of Public Health. Department of Epidemiology
 
  Linda Nichols, Memphis Veterans Affairs Medical Center
 
Funding Agency:United States Department of Health and Human Services. National Institutes of Health. National Institute on Aging
 
Grant Number:AG13265
 
Bibliographic Citation:Schulz, Richard, Louis Burgio, Alan B. Stevens, Robert Burns, Sara Czaja, Dolores Gallagher Thompson, Laura N. Gitlin, Steven Belle, and Linda Nichols. RESOURCES FOR ENHANCING ALZHEIMER'S CAREGIVER HEALTH (REACH II), 2001-2004 [Computer file]. ICPSR04354-v1. Pittsburgh, PA: Richard Schulz, Steven Belle, University of Pittsburgh/Tuscaloosa, AL: Louis Burgio, University of Alabama/College Station, TX: Alan B. Stevens, Texas A&M University/Memphis, TN: Robert Burns, Linda Nichols, Memphis Veterans Affairs Medical Center/Miami, FL: Sara Czaja, University of Miami/Stanford, CA: Dolores Gallagher Thompson, Stanford University/Philadelphia, PA: Laura N. Gitlin, Thomas Jefferson University [producers], 2004. Ann Arbor, MI: Inter-university Consortium for Political and Social Research [distributor], 2006-10-27. doi:10.3886/ICPSR04354
 

Scope of Study

Summary: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.
 
Subject Term(s):Alzheimers disease, caregiver burden, caregivers, dementia, emotional states, families, health status, health care utilization, home health care, intervention, mental disorders, mental health, minorities, older adults, outreach programs, psychological wellbeing, stress
 
Geographic Coverage:Alabama, Birmingham, California, Florida, Memphis, Miami, Palo Alto, Pennsylvania, Philadelphia, Tennessee, United States
 
Time Period:2001 - 2004
 
Date(s) of Collection:2001 - 2004
 
Unit of Observation:caregiver, care-recipient, caregiver/care-recipient dyad
 
Universe:Family caregivers of people with Alzheimer's disease or a related dementia who reside in noninstitutional settings.
 
Data Type:survey data
 
Data Collection Notes:All datasets can be linked using the variable: ID. Dataset 1 (AE: Caregiver/Care Recipient Acute Baseline Alerts/Adverse Events) can be linked to Dataset 2 (AF: Acute Baseline Alerts/Adverse Events Follow-Up Report) using variables: ID, EVENT, and EVEDAT.
 

Methodology

Sample:Convenience sample
 
Mode of Data Collection:personal interview
 

Access and Availability

Note:A list of the data formats available for this study can be found in the summary of holdings. Detailed file-level information (such as record length, case count, and variable count) is listed in the file manifest.
 
Original ICPSR Release:2006-10-27
 
Dataset(s):
  • DS1: AE: Caregiver/Care Recipient Acute Baseline Alerts/Adverse Events Forms Guidebook
  • DS2: AF: Acute Baseline Alerts/Adverse Events Follow-Up Report Guidebook
  • DS3: BA: Baseline Battery Guidebook
  • DS4: BR: Bereavement Battery Guidebook
  • DS5: DA: Intervention Delivery Assessment
  • DS6: DC: Discontinued Battery
  • DS7: FO: Follow-Up Battery
  • DS8: IC: Interventionist Characteristics
  • DS9: OP: Off Protocol Form
  • DS10: PL: Placement Battery
  • DS11: RF: Randomization Form
  • DS12: RT: Care Recipient Tracking Form
  • DS13: SC: Screening Form
  • DS14: SP: Short Portable Mental Status Questionnaire (SPMSQ)