Binge Eating Syndrome Treatment for Older Women (BESTOW)
- Conditions
- Binge Eating
- Interventions
- Behavioral: Binge Eating Syndrome Treatment (BESTOW)
- Registration Number
- NCT05806788
- Brief Summary
Twenty women, ages 60 or older, will be consented and enrolled in a single-arm, pilot implementation trial of the age-tailored cognitive-behavioral based BE intervention. Participants will complete assessments at baseline, post-intervention, and at two follow-up timepoints; weekly BE frequency will be collected to monitor progress during the intervention period.
- Detailed Description
The intervention being studied will be an age-tailored, cognitive-behavioral therapy (CBT) based behavioral intervention for binge eating (BE), delivered by the PI, a licensed clinical psychologist, in small group format (4-6 participants per group) over 12-16 weeks. The intervention will utilize behavioral-based strategies to reduce BE and improve health behaviors, with content including strategies to improve body image, regulation of eating behaviors, and integration of physical activity with an emphasis on body function, health, and longevity. The final session number, frequency, content, and timeline will be determined during intervention-tailoring process not a part of this clinical trial.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 20
- Women
- Age 60 years and over
- Binge eating (BE) ≥1/week during the past ≥3 months
- Community-dwelling
- Able to provide informed consent
- Consistent medication regimen for 3 months
- Significant cognitive impairment
- Nursing home, long-term care facility
- Psychosis or imminent suicide risk
- Current BE treatment
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description BESTOW behavioral intervention Binge Eating Syndrome Treatment (BESTOW) The intervention will utilize behavioral-based strategies to reduce BE and improve health behaviors, with content including strategies to improve body image, regulation of eating behaviors, and integration of physical activity with an emphasis on body function, health, and longevity.
- Primary Outcome Measures
Name Time Method Feasibility - Usage Rating Profile - Intervention 6 weeks (post), and 2 month follow-up Score on the Feasibility Usage Rating Profile. This scale gathers patient reported feasibility of the intervention (e.g., time needed, quality of materials, simplicity of the intervention) to be completed after doing the intervention. This scale has six items; total scores range from 1-6 and a higher scores indicate greater feasibility.
Acceptability - Usage Rating Profile - Intervention 6 weeks (post), and 2 month follow-up Score on the Acceptability Usage Rating Profile scale which gathers participant ratings of how acceptable the treatment is for targeting binge eating (e.g., how helpful the intervention was, how much they liked it, willingness to do the intervention) to be completed after doing the intervention. This scale has eight items; total scores range from 1-6, a higher score indicates greater acceptability.
- Secondary Outcome Measures
Name Time Method Binge Eating Score (BES) Baseline, 6 weeks, 1 month, and 2 month follow-up Change in score on the BES survey. The BES is a 16-item, self-report survey that assess binge eating. Total scores range from 0 to 46, with higher scores meaning more severe binge eating symptoms (Gormally et al., 1982).
Geriatric Depression Scale Score (Center for Epidemiologic Studies-Depression Scale; CES-D) Baseline, 6 weeks (post), 1 month, and 2 month follow-up The CES-D is a 10-item, self-report survey that assess depressive symptoms. Mean scores range from 0 to 3, with higher scores indicating more depressive symptoms (Lewinsohn et al., 1997).
Trial Locations
- Locations (1)
The University of Texas Health Science Center at San Antonio
🇺🇸San Antonio, Texas, United States