What this study is
The goal of this study is to evaluate the efficacy of group-based ACT intervention in improving the levels of psychological distress in caregivers of stroke survivors. The main questions it aims to answer are:
1. Does group-based ACT intervention improve the levels of psychological distress and QoL in family caregivers of stroke survivors? 2. Do the levels of psychological flexibility and experiential avoidance in family caregivers of stroke survivors mediate the outcome of the ACT Group?
The researcher will compare the experimental group (i.e., participants who received group-based ACT intervention) with the control group (i.e., participants who did not receive group-based ACT intervention) to assess whether the group-based ACT intervention is effective in mitigating caregiver stress and improving caregivers' QoL.
Participants in the experimental group will:
1. Receive a 5-weekly, 1.5-hour group intervention based on the ACT Model; 2. Complete study measures at pre-treatment, immediate post-treatment, and 2-month follow-up.
Participants in the control group will not receive the group intervention but will complete the same study measures.
What's being tested
- Group-based ACT Intervention
Intervention · BEHAVIORAL
5-weekly, 1.5-hour group intervention based on the ACT Model
Study details
- Official title
- Effects of Acceptance and Commitment Therapy (ACT) Group for Family Caregivers of Stroke Survivors
- Sponsor
- The Wright Institute
- Conditions
- Caregiver Stress · Caregiver Stress Syndrome · Caregiver Burnout · Caregiver Distress · Caregiver Exhaustion · Caregiver Health Related QOL · Caregiver Burden for Those Who Care for Adults With Impaired Functional Status · Caregiver Quality of Life · Caregiver Burden · Caregiver Mental Health · Caregiver Resilience and Stress · Caregiver Sense of Control Over Life · Caregiver Awareness · Caregiver Stress in Chronic Mental Illness
- Enrolling
- 30 people
- Starts
- 2025-09-01
- Est. completion
- 2028-05-31
- Design
- Single-blind, non-randomized, parallel groups
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 40 Years and overSex ALLHealthy volunteers AcceptedYou may qualify if
- Age 40 or above.
- Taking the primary responsibility for the care of a family member suffering from stroke (i.e. spending at least 70% of the time on performing caregiving tasks).
- The stroke patient has been discharged from hospital and is currently living with the caregiver.
- Having cared for the stroke patient for at least six months, including at least two months after discharge.
- CSAQ score (as determied during pre-group screening meeting) indicates a high level of distress, as evidenced by one of the following: a) participant answered "Yes" to either or both questions 4 and 11; b) total "Yes" scores = 10 or more; c) score on question 17 is 6 or higher; d) score on question 18 is 6 or higher.
- Able to use a computer and has internet access.
- Able to provide informed consent to participate.
You can't join if
- Is below 40 years old.
- Has any comorbid mental disorder or disability that may impede group participation (e.g., personality disorder, learning disability).
- Does not understand English (read, write, listen, and speak).
- Has current active suicidal/homicidal ideation.
- Is currently receiving psychological intervention (individual or group).
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openThe Wright Institute
Alameda, California, United States
- CHI WAI YIU, PsyD Candidate · Contact5109743626jyiu@wi.edu
- CHI WAI YIU, PsyD Candidate · Principal investigator
Recruiting
Study team
Sponsor
The Wright Institute
Study ID WIJYACTSTROKECG
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.