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A Coach-Guided Online Acceptance and Commitment Therapy (ACT) Intervention for Stroke Survivors

The University of Alabama at Birmingham logo

The University of Alabama at Birmingham

Status

Withdrawn

Conditions

Stroke
Depression
Anxiety
Stress

Treatments

Behavioral: acceptance and commitment therapy (ACT)

Study type

Interventional

Funder types

Other

Identifiers

NCT05097040
IRB-300008160

Details and patient eligibility

About

The pilot randomized controlled trial aims to assess effects of a guided online acceptance and commitment therapy (ACT) intervention on distressed stroke survivors compared to the care-as-usual control group. A total of 24 stroke survivors who meet the inclusion criteria will be recruited and randomized to either the intervention group or the control group. Exploratory hypotheses are that the ACT group will show improvements in mental health outcomes (e.g., depressive symptoms, anxiety, and stress), and ACT processes (e.g., psychological flexibility/acceptance) at posttest and 2-month follow-up, compared to the care-as-usual control group. Also, the project will evaluate the feasibility of recruitment, adherence, and retention of participants and explore participants' experiences in the ACT intervention through semi-structured interviews at posttest.

Full description

This pilot randomized controlled trial aims to assess effects of a coach-guided individual online acceptance and commitment therapy (ACT) intervention on distressed stroke survivors compared to the care-as-usual control group. A total of 24 stroke survivors who meet the inclusion criteria will be recruited and randomized to either the intervention group or the control group. The intervention group will receive individual ACT sessions guided by a trained coach for one hour per week over 6 weeks through Zoom videoconferencing. Also, a one-time 1-hour booster session will be provided at 1-month follow-up to facilitate the maintenance of treatment effects. All ACT sessions will be delivered by our ACT coach, a licensed professional counselor (LPC) with substantial clinical experiences and expertise in ACT. Participants assigned to the control group will receive care as usual during the study period. Outcomes regarding mental health and ACT processes will be collected at three time points (i.e., pretest, posttest, and 2-month follow-up) and compared between groups over time. Mental health outcomes and ACT processes will be measured using self-reported questionnaires. A 30-minute individual interview also will be conducted for participants in the intervention group through Zoom videoconferencing to explore participants' experiences in the ACT intervention. The participant demographic information form will be asked to complete at pretest only, asking participants' information such as age, gender, ethnicity/race, level of education, marital status, employment status, and time since stroke.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • community-dwelling adults (aged 18 or above) with a confirmed diagnosis of stroke
  • having at least mild symptoms of psychological distress measured by the Depression, Anxiety and Stress Scale
  • having a computer or a smartphone with internet access at home
  • being able to provide informed consent by understanding the nature of study participation

Exclusion criteria

  • living in a nursing home at time of consent
  • a diagnosis of severe cognitive impairment (e.g., dementia)
  • inability to understand spoken and/or written English
  • having severe communication difficulties (e.g., aphasia and dysarthria) that can impede study participation
  • having a life-threatening illness (e.g. advanced cancer or advanced heart failure) that would make survival for 6 months unlikely
  • having a diagnosis of other central nervous system disorders other than stroke or a severe mental illness (e.g., psychosis)
  • currently receiving a psychological therapy or participating in another study that may affect mental health
  • having a prior experience in ACT
  • having psychiatric hospitalizations or diagnoses of mental illness in the previous two years
  • taking antipsychotic medication at the time of recruitment.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

0 participants in 2 patient groups

Acceptance and commitment therapy (ACT) group
Experimental group
Description:
A total of 7 ACT sessions individually guided by a trained coach through Zoom videoconferencing
Treatment:
Behavioral: acceptance and commitment therapy (ACT)
Control group
No Intervention group
Description:
Care as usual

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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