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Binge Eating Study

A randomized controlled trial of motivational interviewing for binge eating

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN86543360
Enrollment
50
Registered
2013-08-14
Start date
2011-09-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Binge eating disorder

Interventions

Participants in one group participated in a 60-minute therapy session of motivational interviewing (MI) for binge eating, a client-centered therapy designed to increase internal motivation to change b

Sponsors

York University (Canada)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Must meet full or subthreshold (defined as a minimum of 1 binge/week for the past 3 months) DSM-IV diagnostic criteria for Binge Eating Disorder or Bulimia Nervosa, Non-Purging Subtype. 2. Age 18 - 47 years, male and female

Exclusion criteria

Exclusion criteria: 1. Under 18 years of age 2. Substance abuse criteria met 3. Not proficient in English 4. Inconsistent dose of psychiatric medication or have been using psychiatric medication for less than 3 months 5. Active suicidal ideation

Design outcomes

Primary

MeasureTime frame
Changes in binge eating and eating disorder symptoms measured using self-report questionnaires presented in Likert or multiple choice format (Eating Disorder Examination Questionnaire, Binge Eating Scale) at baseline, 1 month, 4 months

Secondary

MeasureTime frame
1. Readiness to change binge eating measured using a self-report Likert questionnaire (University of Rhode Island Stages of Change Assessment) at baseline and immediately following the intervention session 2. Confidence in ability to control binge eating measured using a self-report Likert questionnaire (Weight Efficacy Lifestyle Questionnaire) at baseline and immediately following the intervention session 3. Therapeutic relationship measured using a self-report Likert questionnaire (Working Alliance Inventory), measured immediately following the intervention session Self-Esteem measured using a self-report Likert questionnaire (Rosenberg Self-Esteem Scale) at baseline, 1 month, 4 months 4. Depression measured using a self-report Likert scale questionnaire (Beck Depression Inventory) at baseline, 1 month, 4 months 5. Self-help manual usage measured using a multiple choice questionnaire created for this study at 1 and 4 months

Countries

Canada

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026