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Binge Eating Disorder Treatment Study

Not Applicable
Completed
Conditions
Binge Eating Disorder
Interventions
Behavioral: Group Psychodynamic Interpersonal Psychotherapy
Registration Number
NCT00848367
Lead Sponsor
Ottawa Hospital Research Institute
Brief Summary

The main objective of the proposed study is to determine whether the effectiveness of a group therapy treatment for Binge Eating Disorder (BED) is improved and attrition reduced by optimally matching women with BED who have high attachment anxiety to Group Psychodynamic Interpersonal Psychotherapy (GPIP). This study represents the next phase in a program of research stemming from a previously conducted randomized controlled trial (RCT).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
102
Inclusion Criteria

•Overweight Women 18 years of age or older who binge eat at least twice per week for the past month.

Exclusion Criteria
  • unable speak English
  • history of an eating disorder other than Binge Eating Disorder
  • concurrent Diagnostic and Statistical Manual-IV (DSM-IV) diagnosis of bipolar disorder, psychosis, drug or alcohol problem
  • pregnant or planning on becoming pregnant within the next year
  • are currently or plan to become enrolled in a weight loss program within the next year

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
High attachment anxiety conditionGroup Psychodynamic Interpersonal Psychotherapy16 weeks of Group Psychodynamic Interpersonal Psychotherapy for patients with Binge Eating Disorder, matching them by attachment anxiety dimensions in order to enhance the impact of the therapy. It is hypothesized that by optimally matching patients to groups, they will have better clinical and health outcomes.
Low attachment anxiety conditionGroup Psychodynamic Interpersonal Psychotherapy16 weeks of Group Psychodynamic Interpersonal Psychotherapy for patients with Binge Eating Disorder, matching them by attachment anxiety dimensions in order to enhance the impact of the therapy. It is hypothesized that by optimally matching patients to groups, they will have better clinical and health outcomes.
Primary Outcome Measures
NameTimeMethod
Frequency of Binge Eating in the Past 28 DaysPre and Post treatment, 6 months and 1 year
Secondary Outcome Measures
NameTimeMethod
Depression SymptomsPre and Post treatment, 6 months and 1 year

Early response to treatment is indicated by a reduction in depression symptoms measured by The Beck Depression Inventory II (BDI-II; Beck, Steer, \& Brown, 1996). The BDI-II is scored by summing the ratings for the 21 items. Each item is rated on a 4-point scale ranging from 0 to 3. The range for this scale is 0-63. Higher scores represent more depressive symptoms. We included cases that were missing up to 8 missing items and calculated scores for participants with missing items by taking the weighted mean and multiplying by 21.

Trial Locations

Locations (1)

Regional Centre for the Treatment of Eating Disorders

🇨🇦

Ottawa, Ontario, Canada

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