N/A
N=126
Improving Weight Loss Outcomes for Binge Eating Disorder.
Eating Disorder · Binge-Eating Disorder · Weight Loss · Binge Eating
Bottom Line
View on ClinicalTrials.gov: NCT03712462 ↗Enrolled (actual)
126
Serious AEs
0.0%
Results posted
Apr 2024
Primary outcome: Primary: Weight Loss — 0; 0; -2.13; -2.15 percentage of weight loss
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Acceptance-Based Behavioral Weight Loss Therapy for BED (Behavioral); Standard Behavior Therapy (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Drexel University
- Primary completion
- Feb 2023
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Weight Loss |
0; 0; -2.13; -2.15; -5.46; -5.25 | — |
| SECONDARY Eating Disorder Examination Questionnaire |
2.29; 1.72; 2.49; 1.49; 1.50; 1.60 | — |
Summary
This study aims to develop and evaluate the efficacy of a behavioral weight loss treatment approach for individuals with binge eating disorder to both reduce their binge eating behaviors and lose weight.
Eligibility Criteria
Inclusion Criteria
- Meet the DSM-5 criteria for Binge Eating Disorder
- Have a BMI range of 27-50kg/m2
Exclusion Criteria
- are unable to fluently speak, write, and read English
- are currently experiencing severe psychopathology that would limit their ability to engage in study (e.g., suicidality, substance use disorder, psychotic disorder)
- are unable to engage in moderate physical activity (i.e., walk 2 blocks without rest)
- have a medical condition (e.g., acute coronary syndrome, type I diabetes) that would pose a risk to the participant during intervention, cause a change in weight, or limit ability to comply with the recommendations of the program
- Pregnant or planning to become pregnant in the next 2 years
- Recently began a course of or changed the dosage of medication that can cause significant change in weight
- Have a history of bariatric surgery
- Have had weight loss of > 5% in the past 6 months
Data sourced from ClinicalTrials.gov (NCT03712462). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.