N/A
N=109
Weight Loss Treatment for Veterans With Binge Eating
Binge Eating Disorder
Bottom Line
View on ClinicalTrials.gov: NCT03234881 ↗Enrolled (actual)
109
Serious AEs
0.0%
Results posted
Jun 2024
Primary outcome: Primary: Change in Eating Disorder Examination-Self-report Questionnaire (EDE-Q) — 3.18; 2.89; 2.81; 2.13 score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- MOVE! (Behavioral); MOVE!+CBT (Behavioral)
- Age
- Adult, Older Adult · 21+ yrs
- Sex
- All
- Sponsor
- VA Office of Research and Development
- Primary completion
- May 2023
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change in Eating Disorder Examination-Self-report Questionnaire (EDE-Q) |
3.18; 2.89; 2.81; 2.13; 2.57; 2.00 | — |
| PRIMARY Change in Binge Episodes From Eating Disorder Examination Interview |
21.23; 21.75; 7.02; 3.64; 6.02; 5.38 | — |
| SECONDARY Change in Patient Health Questionnaire-9 (PHQ-9) |
9.44; 8.41; 7.89; 5.38; 7.95; 6.92 | — |
| SECONDARY Change in PTSD Checklist (PCL-5) |
37.48; 31.27; 27.67; 22.62; 29.29; 28.46 | — |
| SECONDARY Weight and Eating Quality of Life (WE-QoL) |
1.58; 1.50; 1.29; 1.12; 1.33; 1.05 | — |
| SECONDARY Change in European Quality of Life (EuroQoL-5D) |
56.8; 52.8; 63; 69.05; 66.35; 68.07 | — |
| SECONDARY Night Eating Questionnaire (NEQ) |
21.06; 21.25; 18.89; 15.70; 17.89; 16.98 | — |
| SECONDARY CBT Session Attendance (Treatment Dose) |
7.75 | — |
Summary
This study aims to adapt and test a cognitive behavioral therapy (CBT) treatment that can be administered concurrently with the Veteran's Health Administration (VHA) MOVE! weight management program for Veterans with DSM-5 Binge Eating Disorder (BED) and high weight.
Eligibility Criteria
Inclusion Criteria
- BMI>=25
- Presence of recurrent binge eating on the MOVE! Survey
Exclusion Criteria
- More than 4 MOVE! sessions in the prior year
- Active psychosis or suicidal ideation
- Medical or psychiatric illness, or cognitive deficits that interfere with providing consent or completing assessments
- Pregnancy or lactation
Data sourced from ClinicalTrials.gov (NCT03234881). 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.