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Online Caregiver Psychoeducation and Support for Alzheimer's

Primary Purpose

Alzheimer's Disease

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
caregiver website support
caregiver brief supportive phone calls
Sponsored by
US Department of Veterans Affairs
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alzheimer's Disease focused on measuring technology development and assessment, internet, randomized control trial

Eligibility Criteria

18 Years - 95 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient living in community and ambulatory
  • Patient has diagnosis of Alzheimer's disease
  • Patient age 50-95
  • Caregiver age 18-90
  • Patient currently under treatment for Alzheimer's disease
  • Patient and caregiver reside within 2 hours of Los Angeles
  • Caregiver has home internet access
  • Patient has close contact with caregiver

Exclusion Criteria:

  • Patient lives in residential setting
  • No family contact
  • Acute illness or chronic disease in patient or caregiver
  • Patient or caregiver plans to leave area within the year

Sites / Locations

  • VA Greater Los Angeles Healthcare System, West LA

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

caregiver website support

caregiver brief supportive phone calls

Arm Description

caregiver access to website support for 6 months embedded in one year of customary care

caregiver brief supportive telephone calls for 6 months embedded in one year of customary care

Outcomes

Primary Outcome Measures

Change in Caregiver Burden From Baseline
Total score on the Zarit Short Burden Scale, a 12 item instrument that utilizes a likert scale 1-5 rating of frequency. The range is 12 (never) to 60 (nearly always) wherein higher scores are more indicative of caregiver burden.
Change in Frequency of Patient Problematic Behavioral Patterns From Baseline
Total Score on the Frequency of Problematic Behaviors on the Revised Memory and Behavior Problem Checklist. The Revised Memory and Behavior Checklist is a 24 item instrument that measures the frequency of a behavior on a 0-4 likert scale wherein higher numbers indicate greater frequency. The range is 0-96.
Change in Caregiver Negative Reactions to Problematic Behavioral Patterns From Baseline
Total Score on the Negative Reactions Scale from the Revised Memory and Behavior Problem Checklist. The scale measures the caregiver's level of reaction to a series of potential problematic behaviors on a 0-4 likert scale; higher numbers indicate a greater degree of distress. The range is 0-96.
Change in Caregiver Depression From Baseline
Total score on the Beck Depression Inventory. The Beck Depression Inventory is a 21 item likert scale instrument with a total range of 0 to 63. Higher scores are indicative of increased endorsement of depressive symptoms. Additionally, it utilizes a cutoff score of13 to indicate probable depression

Secondary Outcome Measures

Change in Caregiver Report of Patient Medication Adherence From Baseline
Adherence to prescribed medication regimen rated by caregiver on a 1 (0%) to 5 (100%) scale. Higher scores indicate better adherence. Values in statistical table below are least square estimates, and thus may be slightly out-of-range of actual respondent choices on scale.

Full Information

First Posted
December 22, 2006
Last Updated
April 7, 2015
Sponsor
US Department of Veterans Affairs
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1. Study Identification

Unique Protocol Identification Number
NCT00416078
Brief Title
Online Caregiver Psychoeducation and Support for Alzheimer's
Official Title
Caregiver Psychoeducation and Support: Improving Outcomes in AD/ADRD
Study Type
Interventional

2. Study Status

Record Verification Date
April 2015
Overall Recruitment Status
Completed
Study Start Date
August 2007 (undefined)
Primary Completion Date
June 2012 (Actual)
Study Completion Date
December 2012 (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
This study is piloting an internet-based intervention to provide support for caregivers of VA patients with Alzheimer's disease or related memory difficulties (ADRD). Veterans with a clinical diagnosis of ADRD and their caregiver/relatives will be randomized to receive one of two interventions: (1) customary care (cc) and access to an intensive, interactive online education and support website intervention for 6 months, or (2) cc and monthly brief telephone calls with project staff for six month. It is hypothesized that participation in the intensive intervention will result in a reductions in patient problematic behavior and caregiver responses to it, reduced caregiver burden and depression, and improved medication adherence at the end of treatment, and more patients remaining at home through the 12 months post-randomization period..
Detailed Description
Alzheimer's disease (AD) is a progressive brain disease resulting in cognitive and functional decline. While some pharmacological agents and behavioral programs are now available to slow the rate of decline, there is no cure. Caregivers, who typically are the female spouses or daughters of afflicted individuals, must confront both the deterioration of a loved one, and that person's need for increasingly demanding care. Caregivers tend to experience high levels of depression, anxiety, and burden. Data suggest that providing education, social support, and ongoing professional consultation to families involved in the care of a relative with AD results in improvement in caregiver psychological status, and sometimes even slows the functional decline of the patient. Recent technological advancements in video conferencing, online communication, and streaming audio/video presentations, which are increasingly easy to use and gaining widespread acceptance among mental health professionals as well as the public, have given rise to a great deal of interest in telemedicine and telepsychiatry. This study tested an Internet-based family intervention for AD that relatives can access from their homes with ease, and at no cost. In addition to improving patient outcomes through instruction of effective behavioral management, we proposed that participation in an Internet program would also reduce caregiver depression and burden. Fifty-three veterans with a clinical diagnosis of AD and their caregiver/relatives were randomized to receive one of two interventions: (1) customary care (cc) and access to an intensive, interactive online education and support website intervention for 6 months, or (2) cc and monthly brief telephone calls with project staff for 6 months. We hypothesized that, at the end of the active intervention, participation in the intensive intervention would result reduced patient problematic behavior, caregiver burden, depression, and negative responses to problematic patient behaviors, as well as improved patient medication compliance. At 12 month follow-up, we hypothesized access to the online program would result in more patients remaining at home. The overriding longterm project objective was to develop an effective online education and support program for caregivers of patients with AD that can be manualized, replicated, and disseminated to other clinical and research centers, within both the VA health care system and the community, to enhance the efficiency and effectiveness of psychosocial treatment in AD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer's Disease
Keywords
technology development and assessment, internet, randomized control trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
53 (Actual)

8. Arms, Groups, and Interventions

Arm Title
caregiver website support
Arm Type
Experimental
Arm Description
caregiver access to website support for 6 months embedded in one year of customary care
Arm Title
caregiver brief supportive phone calls
Arm Type
Active Comparator
Arm Description
caregiver brief supportive telephone calls for 6 months embedded in one year of customary care
Intervention Type
Behavioral
Intervention Name(s)
caregiver website support
Intervention Description
caregiver access to website support for 6 months embedded in one year of customary care
Intervention Type
Behavioral
Intervention Name(s)
caregiver brief supportive phone calls
Intervention Description
caregiver brief supportive telephone calls for 6 months embedded in one year of customary care
Primary Outcome Measure Information:
Title
Change in Caregiver Burden From Baseline
Description
Total score on the Zarit Short Burden Scale, a 12 item instrument that utilizes a likert scale 1-5 rating of frequency. The range is 12 (never) to 60 (nearly always) wherein higher scores are more indicative of caregiver burden.
Time Frame
baseline to end-of-treatment (6 months)
Title
Change in Frequency of Patient Problematic Behavioral Patterns From Baseline
Description
Total Score on the Frequency of Problematic Behaviors on the Revised Memory and Behavior Problem Checklist. The Revised Memory and Behavior Checklist is a 24 item instrument that measures the frequency of a behavior on a 0-4 likert scale wherein higher numbers indicate greater frequency. The range is 0-96.
Time Frame
baseline to end of treatment (6 months)
Title
Change in Caregiver Negative Reactions to Problematic Behavioral Patterns From Baseline
Description
Total Score on the Negative Reactions Scale from the Revised Memory and Behavior Problem Checklist. The scale measures the caregiver's level of reaction to a series of potential problematic behaviors on a 0-4 likert scale; higher numbers indicate a greater degree of distress. The range is 0-96.
Time Frame
baseline to end of treatment (6 months)
Title
Change in Caregiver Depression From Baseline
Description
Total score on the Beck Depression Inventory. The Beck Depression Inventory is a 21 item likert scale instrument with a total range of 0 to 63. Higher scores are indicative of increased endorsement of depressive symptoms. Additionally, it utilizes a cutoff score of13 to indicate probable depression
Time Frame
baseline to end-of-treatment (6 months)
Secondary Outcome Measure Information:
Title
Change in Caregiver Report of Patient Medication Adherence From Baseline
Description
Adherence to prescribed medication regimen rated by caregiver on a 1 (0%) to 5 (100%) scale. Higher scores indicate better adherence. Values in statistical table below are least square estimates, and thus may be slightly out-of-range of actual respondent choices on scale.
Time Frame
baseline to end-of-treatment (6 months)
Other Pre-specified Outcome Measures:
Title
Number of Participants Placed in Assisted Living or Nursing Homes 12 Months From Baseline
Description
Frequency count of individuals placed in assisted living or nursing homes
Time Frame
baseline to end-of-follow-up (12 months from baseline)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
95 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient living in community and ambulatory Patient has diagnosis of Alzheimer's disease Patient age 50-95 Caregiver age 18-90 Patient currently under treatment for Alzheimer's disease Patient and caregiver reside within 2 hours of Los Angeles Caregiver has home internet access Patient has close contact with caregiver Exclusion Criteria: Patient lives in residential setting No family contact Acute illness or chronic disease in patient or caregiver Patient or caregiver plans to leave area within the year
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Theodore J. Hahn, MD
Organizational Affiliation
VA Greater Los Angeles Healthcare System, West LA
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Greater Los Angeles Healthcare System, West LA
City
West Los Angeles
State/Province
California
ZIP/Postal Code
90073
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
22662739
Citation
Hayden LJ, Glynn SM, Hahn TJ, Randall F, Randolph E. The use of Internet technology for psychoeducation and support with dementia caregivers. Psychol Serv. 2012 May;9(2):215-8. doi: 10.1037/a0027056.
Results Reference
result
PubMed Identifier
33417236
Citation
Gonzalez-Fraile E, Ballesteros J, Rueda JR, Santos-Zorrozua B, Sola I, McCleery J. Remotely delivered information, training and support for informal caregivers of people with dementia. Cochrane Database Syst Rev. 2021 Jan 4;1(1):CD006440. doi: 10.1002/14651858.CD006440.pub3.
Results Reference
derived

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Online Caregiver Psychoeducation and Support for Alzheimer's

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