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Clinical Trials/NCT02584101
NCT02584101CompletedNot Applicable

The Use of Acceptance and Commitment Therapy to Promote WellBeing and Psychological Flexibility in Carers: A Randomized Controlled Feasibility Trial

University of Glasgow1 site in 1 country18 target enrollmentStarted: January 1, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
18
Locations
1
Primary Endpoint
Well-being

Study Overview

Brief Summary

Background: Research has extensively documented the adverse impact that caring for an individual with an acquired brain injury can have including financial difficulties, social isolation, family tension and conflict, relationship difficulties, role adjustment and psychological distress (Foster et al., 2012). Research has indicated that Acceptance and Commitment Therapy (ACT) shows promise for increasing wellbeing and psychological flexibility in caregivers and could be a useful intervention for use with this population.

Aims: The primary aim of this study is to investigate the feasibility of using an ACT intervention to enhance the wellbeing and the psychological flexibility of carers using the Population, Intervention, Control, and Outcomes (PICO) framework. Methods: The current study is a randomised control design, exploring the feasibility of comparing the efficacy of an ACT intervention to Enhanced Treatment As Usual (ETAU), to improve the wellbeing of the carers of adults with an acquired brain injury (ABI). Participants will be recruited from the Brain Injury Rehabilitation Trust (BIRT) in Glasgow, Scotland and randomly assigned to either an ACT intervention group or TAU control group. Both will be assessed in parallel to one another completing a range of baseline and post-baseline measures. Applications: This feasibility study will provide information for further research on the utilisation of an ACT intervention to improve the wellbeing of carers and whether this is an acceptable intervention for this population.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •full time or part time carer for an adult with an acquired brain injury

Exclusion Criteria

  • •learning disability
  • •not proficient in English

Arms & Interventions

ACT

Experimental

ACT therapy

Intervention: ACT (Behavioral)

Enhanced Treatment as Usual

Active Comparator

Group support

Intervention: Enhanced Treatment as Usual (Behavioral)

Outcomes

Primary Outcomes

Well-being

Time Frame: 4 weeks

Change in General Health Questionnaire (GHQ-12) score

Secondary Outcomes

  • Psychological Flexibility(4 weeks)
  • Values(4 weeks)
  • Experiential Avoidance(4 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ross White

Senior Lecturer

University of Glasgow

Study Sites (1)

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