Online Caregiver Psychoeducation and Support for Alzheimer's

NCT ID: NCT00416078

Last Updated: 2015-04-29

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2/PHASE3

Total Enrollment

53 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-08-31

Study Completion Date

2012-12-31

Brief Summary

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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

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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.

Conditions

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Alzheimer's Disease

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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caregiver website support

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

Group Type EXPERIMENTAL

caregiver website support

Intervention Type BEHAVIORAL

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

caregiver brief supportive phone calls

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

Group Type ACTIVE_COMPARATOR

caregiver brief supportive phone calls

Intervention Type BEHAVIORAL

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

Interventions

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caregiver website support

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

Intervention Type BEHAVIORAL

caregiver brief supportive phone calls

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

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

95 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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US Department of Veterans Affairs

FED

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Theodore J. Hahn, MD

Role: PRINCIPAL_INVESTIGATOR

VA Greater Los Angeles Healthcare System, West LA

Locations

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VA Greater Los Angeles Healthcare System, West LA

West Los Angeles, California, United States

Site Status

Countries

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United States

References

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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.

Reference Type RESULT
PMID: 22662739 (View on PubMed)

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.

Reference Type DERIVED
PMID: 33417236 (View on PubMed)

Other Identifiers

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IIR 05-107

Identifier Type: -

Identifier Source: org_study_id

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