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Clinical Trials/NCT03552159
NCT03552159
Completed
Not Applicable

Behavioral Activation for Dementia Caregivers: Scheduling Pleasant Events and Enhancing Communications

The Hong Kong Polytechnic University0 sites96 target enrollmentDecember 1, 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dementia Caregivers
Sponsor
The Hong Kong Polytechnic University
Enrollment
96
Primary Endpoint
Depressive Symptoms
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This project was designed to test a model targeted intervention for dementia caregivers telephone program consisting of both psychoeducation and behavioral activation components to reduce the burden of caregivers. The program is delivered by telephone to increase accessibility and sustainability for caregivers.

Detailed Description

The study compared two telephone interventions using a four-month longitudinal randomized controlled trial. For the first four weeks, all participants received the same psychoeducation program via telephone. Then for the following four months, eight biweekly telephone follow-up calls were carried out. For these eight follow-up calls, participants were randomized into either one of the two following groups with different conditions. For the Psychoeducation with BA (PsyED-BA) group, participants would receive eight biweekly sessions of BA practice focused on pleasant event scheduling and improving communications. For the Psychoeducation only (PsyED Only) group, there would be eight biweekly sessions of general discussion of psychoeducation and related information

Registry
clinicaltrials.gov
Start Date
December 1, 2012
End Date
June 30, 2016
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • They were caregivers aged 25 or above and must have be caring for a care recipient diagnosed with Alzheimer's disease for at least 3 months. They should be the primary caregiver and a spouse, kin (e.g. daughter/son or daughter/son-in-law) or sibling of the care recipient.

Exclusion Criteria

  • To ensure intervention fidelity, participants who showed signs of severe intellectual deficits, demonstrate suicidal ideation, exhibit evidence of psychotic disorders, or cannot read or speak fluent Chinese / Cantonese were excluded.

Outcomes

Primary Outcomes

Depressive Symptoms

Time Frame: Change from baseline through study completion, an average of about 5 months

Measured by CES-D

Secondary Outcomes

  • Sense of Burden(Change from baseline through study completion, an average of about 5 months)

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