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Clinical Trials/NCT03348475
NCT03348475
Completed
Not Applicable

Binge Focused Therapy: Examining an Accessible, Cost-effective, Guided, Self-help, Group-based Approach for the Treatment of Binge Eating Disorder

Nova Scotia Health Authority1 site in 1 country38 target enrollmentFebruary 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Binge-Eating Disorder
Sponsor
Nova Scotia Health Authority
Enrollment
38
Locations
1
Primary Endpoint
Change in Binge Eating Frequency
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The "Brain Over Binge Recovery Guide" (Hansen, 2016), is a self-help approach that incorporates fundamental aspects of Acceptance and Commitment Therapy, Dialectical Behavioural Therapy, Motivational Enhancement Therapy and addictions treatment. This approach has been streamlined into a guided self-help protocol (Binge Focused Therapy, or BFT) that can be delivered by undergraduate students with minimal mental health experience in 3 group sessions spread over 8 weeks (i.e., Week 1, Week 2, Week 8). The aim of this proof-of-concept study is to provide preliminary data to examine whether this approach is feasible and has clinical potential for patients with binge eating disorder.

Registry
clinicaltrials.gov
Start Date
February 1, 2018
End Date
October 3, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Aaron Keshen

Psychiatrist

Nova Scotia Health Authority

Eligibility Criteria

Inclusion Criteria

  • Age 18 years or older;
  • Meets DSM-5 criteria for moderate to severe Binge Eating Disorder (BED) as determined through screening interview by an eating disorder psychiatrist and validated with the Eating Disorder Diagnostic Scale (a self-report screening tool);
  • Provides written informed consent.

Exclusion Criteria

  • Currently receiving treatment for BED;
  • Is taking a psychotropic medication (e.g., antidepressant, stimulant, etc.) AND the dose has been changed 2 weeks prior to baseline;
  • Insufficient knowledge of English.

Outcomes

Primary Outcomes

Change in Binge Eating Frequency

Time Frame: Baseline, Week 8, 1-year follow-up

Self-reported binge eating frequency will be assessed with the Eating Disorder Examination Questionnaire 6.0 (EDE-Q). Binge eating frequency is measured on item 15 of the EDE-Q.

Secondary Outcomes

  • Change in Binge Eating Severity(Baseline, Week 2, Week 8, 1-year follow-up)
  • Change in General Eating Disorder Symptomatology(Baseline, Week 8, 1-year follow-up)
  • Motivation/Confidence/Readiness for Behaviour Change(Baseline and Week 2)
  • Participant Satisfaction with Intervention(Week 8)
  • Remission Rate(Week 8, 1-year follow up)
  • Response Rate(Week 8, 1-year follow up)
  • Change in Locus of Control of Behaviour(Baseline, Week 2, Week 8, 1-year follow-up)
  • Change in Coping Self-Efficacy(Baseline, Week 2, Week 8, 1-year follow-up)
  • Depression, Anxiety and Tension/Stress(Baseline)
  • Week 3 - 7 Adherence(Week 8)

Study Sites (1)

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