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Evaluating an Online Acceptance and Commitment Training Program for Individuals with Chronic Health Conditions

U

Utah State University

Status

Completed

Conditions

Depression
Stress, Psychological
Well-Being, Psychological

Treatments

Behavioral: ACT Guide for Chronic Health Conditions

Study type

Interventional

Funder types

Other

Identifiers

NCT06179264
IRB: #13890

Details and patient eligibility

About

Chronic health conditions (CHC) commonly share the challenge of impaired health-related quality of life, negatively impacting the lives of millions of people in the United States. Long term effects for living with a chronic health condition are likely to include poor self-management behaviors, which are related to avoidance of disease related thoughts and feelings (e.g., health anxiety) and can be addressed directly with psychosocial interventions. With the focus on fostering values driven and meaningful behavior while accepting thoughts and feelings, ACT may prove to be a particularly effective approach for individuals coping with the challenging symptoms and effects of having a chronic health condition. Previous web-based ACT interventions for CHCs have focused on building ACT skills for a narrow subset of CHCs (e.g., breast cancer, diabetes, tinnitus). While there is added benefit for a self-help program for populations with specific stressors or conditions, there is also a high prevalence of comorbidity in CHCs, shared challenges in illness management and coping, and clear evidence that ACT works effectively across CHCs to improve quality of life. Thus, our goal of this research project is to evaluate a new 6 session, online, self-guided ACT program for adults with chronic health conditions broadly to improve their quality of life and wellbeing through a randomized controlled trial. The specific aims are:

  1. To evaluate the feasibility of an initial prototype of ACT program for adults with CHC's as indicated by recruitment, retention, and adherence rates.
  2. To evaluate the acceptability as indicated by self-reported program satisfaction and qualitative feedback following the course completion.
  3. To identify ways to further refine the program based on participant self-reported satisfaction with sessions and open-ended text-based feedback.
  4. To test the efficacy of the program on improving quality of life among adults with CHC's.

Enrollment

101 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • ≥ 18 years old
  • Currently living in the U.S.
  • Self-report having at least 1 chronic health condition (e.g., cardiovascular disease, cancer, diabetes, chronic pain, rheumatoid arthritis, HIV, Parkinson's disease, irritable bowel syndrome, Crohn's disease, chronic obstructive pulmonary disease, multiple sclerosis)
  • Self-report having had the chronic health condition for ≥ 3 months
  • Can access the internet via computer, mobile phone, or tablet
  • Have an interest in using an online mental health intervention

Exclusion criteria

• Not fluent in reading English (at this point the online program can only be feasibly and competently delivered in English)

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

101 participants in 2 patient groups

Treatment
Experimental group
Description:
Following random assignment to the condition after completing baseline assessment, participants will be instructed to complete the ACT Guide for Chronic Health Conditions program over the next 6 weeks.
Treatment:
Behavioral: ACT Guide for Chronic Health Conditions
Waitlist Control
No Intervention group
Description:
Following random assignment to the condition after completing baseline assessment, participants will be instructed to wait to receive the intervention after a period of 10 weeks (this accounts for the 6 weeks that treatment condition participants are given to complete the program, plus the 4 interim between post-assessment and follow-up.

Trial contacts and locations

1

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Central trial contact

Michael E Levin, PhD; Ty B Aller, PhD

Data sourced from clinicaltrials.gov

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