search
Back to results

Testing the Effectiveness of Telephone Support for Dementia Caregivers (CONNECT)

Primary Purpose

Dementia, Alzheimer Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Telephone Support
Sponsored by
US Department of Veterans Affairs
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dementia focused on measuring Caregiver, Dementia, Alzheimer Disease, Telephone, Randomized Controlled Trials

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Caregiver Age: 21 years or older Family member of the care recipient Must live with care recipient or share cooking facilities Must have a telephone Must plan to remain in the area for the duration of the intervention and follow-up Caregiver role for more than 6 months Must provide an average of 4 hours of supervision or direct assistance per day for the care recipient Risk Screening Tool: must have a total score of at least 1 for question 36, and a total of at least 2 for questions 38-40 (on the Screening Form) Care Recipient NINCDS (MD diagnosis) or cognitive impairment (raw score on MMSE of 23 or less) Must be a Veteran with dementia or being cared for by a Veteran who receives services at the Memphis VAMC Exclusion Criteria: Caregiver Active treatment (chemotherapy; radiation therapy) for cancer Imminent placement of care recipient into a nursing home (within 6 months) SPMSQ: > 4 errors Care Recipient History of Parkinson's Disease or a stroke with no reported decline in memory over the past year Active treatment (chemotherapy or radiation therapy) for cancer More than three acute medical hospitalizations in the past year (other than psychiatric or Alzheimer's Disease related admissions) Schizophrenia (onset of delusions before age 45) or other severe mental illness Dementia secondary to head trauma (probable) Blindness or deafness if either disability prohibits them from data collection or participation in the interventions MMSE = 0 and Bedbound (routinely confined to bed or chair for at least 22 hours a day, for at least 4 of the last 7 days) Planned nursing home admission in 6 months

Sites / Locations

  • Memphis VA Medical Center, Memphis, TN

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Arm 1

Arm 2

Arm Description

Telephone support groups

Usual VA care

Outcomes

Primary Outcome Measures

General well-being (revised Rand General Well-Being Scale); and caregiver's level of distress with care recipient behaviors (Revised Memory and Behavior Problems Checklist). Data is collected at baseline, 6 and 12 months in a face to face interview.

Secondary Outcome Measures

Cost-Effectiveness
Time spent providing care

Full Information

First Posted
July 5, 2005
Last Updated
April 6, 2015
Sponsor
US Department of Veterans Affairs
search

1. Study Identification

Unique Protocol Identification Number
NCT00119561
Brief Title
Testing the Effectiveness of Telephone Support for Dementia Caregivers
Acronym
CONNECT
Official Title
Testing the Effectiveness of Telephone Support for Dementia Caregivers
Study Type
Interventional

2. Study Status

Record Verification Date
July 2014
Overall Recruitment Status
Completed
Study Start Date
February 2005 (undefined)
Primary Completion Date
June 2007 (Actual)
Study Completion Date
January 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
US Department of Veterans Affairs

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary goal of the study is documentation of effectiveness of telephone support groups to reduce caregiver burden and stress. Caregivers who participate in intervention (Telephone Support) should experience lower levels of stress, burden and health care utilization (lower use of psychotropic drugs, fewer scheduled/unscheduled medical visits, lower rates of institutionalization, more efficient use of time in managing care recipient problems) compared to those caregivers in Usual Care.
Detailed Description
Background: Caregiving can severely limit caregivers' lives. In order to keep their family member at home, dementia caregivers often experience physical and psychological strain, social isolation, loss of time for self, and inability to obtain and/or afford assistance with caregiving tasks. The amount of time spent in providing care for a family member with dementia contributes to these problems. Dementia caregivers report spending around 18 hours per day in caregiving tasks and 3 hours per day in supervision. The high levels of stress involved in caring for a dementia patient and the widespread lack of training in such care can lead to a vicious cycle of ever-increasing health care dependency, first for the patient and secondly for informal caregivers. Telephone Support Groups have the potential to address caregivers' stress, isolation and education about dementia and its management, leading to sustainable informal caregiving and lower healthcare use and overall VHA expenditures for the veteran patient with dementia. Objectives: Study objectives are to 1) examine Telephone Support Groups' effectiveness for caregivers, 2) determine whether Telephone Support results in decreases in VHA health care use and costs for the veteran, and decreased VHA and/or non-VHA use and costs for the caregiver, and 3) examine the intervention's effect on caregivers' time spent providing care. The long-term objective is to develop and disseminate the protocol and materials for effective Telephone Support Groups that can be used across the VHA system. Methods: This randomized clinical trial of 154 caregivers (Black/African American, White/Caucasian, rural, urban) compared dementia caregivers participating in Telephone Support Groups to caregivers whose family members with dementia were receiving usual care. Either the caregiver or the patient had to be a veteran receiving care at the VAMC Memphis. In the treatment condition, there were 15 year-long support groups of one trained group leader and 5 to 6 caregivers. Each support group met 14 times. The one hour calls were semi-structured conference calls with education, coping skills and cognitive restructuring, and support components. A Caregiver Notebook with information on each topic provided materials for the educational sessions. Topics included knowledge of dementia, safety, caregiver health and well being, communication, managing behavioral challenges, and caregiver stress and coping. A workshop focusing on the same behavior management and stress topics was offered to Usual Care caregivers at the end of their participation. Data were collected in caregivers' homes by trained Research Associates at baseline, six and twelve months. VHA health care use and data for the veteran were based on the Patient Treatment File (PTF) and the Outpatient Clinic File (OPC) and costs data used the Health Economics Resource Center (HERC) Average Cost Data Sets.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dementia, Alzheimer Disease
Keywords
Caregiver, Dementia, Alzheimer Disease, Telephone, Randomized Controlled Trials

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
154 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm 1
Arm Type
Experimental
Arm Description
Telephone support groups
Arm Title
Arm 2
Arm Type
No Intervention
Arm Description
Usual VA care
Intervention Type
Behavioral
Intervention Name(s)
Telephone Support
Intervention Description
Each telephone support group of 5 caregivers and a group leader met 14 times over a year. The hour calls were semi-structured with an educational component and a support component, led by a trained Group Leader. Topics included knowledge of dementia, safety, caregiver health and well being, communication, managing behavioral challenges and caregiver stress and coping.
Primary Outcome Measure Information:
Title
General well-being (revised Rand General Well-Being Scale); and caregiver's level of distress with care recipient behaviors (Revised Memory and Behavior Problems Checklist). Data is collected at baseline, 6 and 12 months in a face to face interview.
Time Frame
6 and 12 months
Secondary Outcome Measure Information:
Title
Cost-Effectiveness
Time Frame
6 and 12 months
Title
Time spent providing care
Time Frame
6 and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Caregiver Age: 21 years or older Family member of the care recipient Must live with care recipient or share cooking facilities Must have a telephone Must plan to remain in the area for the duration of the intervention and follow-up Caregiver role for more than 6 months Must provide an average of 4 hours of supervision or direct assistance per day for the care recipient Risk Screening Tool: must have a total score of at least 1 for question 36, and a total of at least 2 for questions 38-40 (on the Screening Form) Care Recipient NINCDS (MD diagnosis) or cognitive impairment (raw score on MMSE of 23 or less) Must be a Veteran with dementia or being cared for by a Veteran who receives services at the Memphis VAMC Exclusion Criteria: Caregiver Active treatment (chemotherapy; radiation therapy) for cancer Imminent placement of care recipient into a nursing home (within 6 months) SPMSQ: > 4 errors Care Recipient History of Parkinson's Disease or a stroke with no reported decline in memory over the past year Active treatment (chemotherapy or radiation therapy) for cancer More than three acute medical hospitalizations in the past year (other than psychiatric or Alzheimer's Disease related admissions) Schizophrenia (onset of delusions before age 45) or other severe mental illness Dementia secondary to head trauma (probable) Blindness or deafness if either disability prohibits them from data collection or participation in the interventions MMSE = 0 and Bedbound (routinely confined to bed or chair for at least 22 hours a day, for at least 4 of the last 7 days) Planned nursing home admission in 6 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Linda Olivia Nichols, PhD
Organizational Affiliation
Memphis VA Medical Center, Memphis, TN
Official's Role
Principal Investigator
Facility Information:
Facility Name
Memphis VA Medical Center, Memphis, TN
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38104
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
22917945
Citation
Nichols LO, Martindale-Adams JL, Burns R, Graney MJ, Zuber JK, Kennedy SE. Potential explanations for control group benefit. Clin Trials. 2012 Oct;9(5):588-95. doi: 10.1177/1740774512455876. Epub 2012 Aug 23.
Results Reference
result
PubMed Identifier
24617278
Citation
Martindale-Adams J, Nichols LO, Burns R, Graney MJ, Zuber J. A trial of dementia caregiver telephone support. Can J Nurs Res. 2013 Dec;45(4):30-48. doi: 10.1177/084456211304500404.
Results Reference
result

Learn more about this trial

Testing the Effectiveness of Telephone Support for Dementia Caregivers

We'll reach out to this number within 24 hrs