Alzheimer's Caregivers |
Caregivers for Alzheimer's Disease |
Clinical Trial: Evaluating the Carter Institute Caregiver Education Program at the VA
This study is not yet open for patient recruitment.
Verified by Department of Veterans Affairs August 2005
|
Purpose
| Condition | Intervention |
|---|---|
| Caregivers | Behavior: Caregiver education program |
MedlinePlus consumer health information
Study Type: Interventional
Study Design: Educational/Counseling/Training, Non-Randomized, Single Blind, Active Control, Factorial Assignment, Efficacy Study
Secondary Outcomes: 1. To lay a foundation for widespread implementation of the program, including feasibility, cost, and health utility gains for informal caregivers; 2. To explore characteristics of veterans and their family caregivers that influence immediate and long-range outcomes of the intervention.
Expected Total Enrollment: 195
Study start: October 2005; Expected completion: September 2008
Last follow-up: November 2007; Data entry closure: February 2008
This project will implement and evaluate the Rosalyn Carter Institute’s (RCI’s) educational and support program for caregivers, “Caring for You, Caring for Me.” Specifically, it will examine effects of the program upon family caregivers to elderly veterans receiving outpatient primary care at the Atlanta Veterans Affairs Medical Center (VAMC).
Thus, this project has the potential not only to enhance the VA’s complement of services for older veterans and their families, but also to demonstrate clearly the strengths of the RCI program.
Primary objectives of the research are:
- to evaluate user satisfaction with and perceived utility of the “Caring for You, Caring for Me” caregiver educational program among formal (VHA staff) and informal (family) caregivers who undergo the program;
- to assess effects of the program upon psychosocial and physical well-being of informal caregivers over a 1-year period,
- to estimate effects of the program upon health status and service utilization of veterans whose family caregivers undergo the caregiver intervention, and
- to determine whether an augmentation of the program, using structured follow-up to help caregivers apply program principles and knowledge, enhances its effects upon outcomes to caregivers and veterans.
The project has two secondary objectives, designed to build a foundation for further research by elucidating selected processes and effects of the intervention upon caregivers’ and veterans’ well-being. They are:
- To lay a foundation for widespread implementation of the program, including feasibility, cost, and health utility gains for informal caregivers, and
- To explore characteristics of veterans and their family caregivers that influence immediate and long-range outcomes of the intervention.
Eligibility
Inclusion Criteria:
Family members of veterans Aged 65+ years and receiving care through the Atlanta VAMC’s Bronze (geriatric primary care) Clinic. Must be the primary Family Caregiver to the veteran Must have been assisting with at least one activity of daily living (ADL) for at least 6 months prior to beginning the intervention.
Exclusion Criteria:
Caregivers are automatically excluded if veteran has a terminal illness with six months or less to live. -
Location and Contact Information
Laura S Britan, MPH 404-321=6111 Ext. 6477 Laura.Britan@va.gov
Georgia
Atlanta VA Medical center, Decatur, Georgia, 30033, United States
Ronald Schuchard, PhD 404-728-5063 Ronald.Schuchard@va.gov
Patricia Parmelee, PhD, Principal Investigator, Atlanta VA Medical Center
More Information
Last Updated: December 29, 2005
Record first received: December 29, 2005
ClinicalTrials.gov Identifier: NCT00271375
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2006-01-10

Not Signed In -


