Actively Recruiting
Treating Binge Eating and Obesity Digitally in Black Women: A Feasibility Study
Led by University of North Carolina, Chapel Hill · Updated on 2025-08-27
60
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of North Carolina, Chapel Hill
Lead Sponsor
N
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are investigating a digital health program designed for Black women with obesity who experience binge eating. This study aims to adapt a validated treatment to be culturally relevant and accessible in primary care settings, where Black women often receive care for eating and weight concerns. The research addresses the need for effective, tailored interventions as Black women with obesity face higher rates of binge eating and related health risks but have been underrepresented in treatment trials. The study involves a randomized trial comparing two remote interventions delivered via smartphone app, online lessons, and Zoom. One group receives the Centering Appetite program, which combines appetite awareness treatment and behavioral weight loss over six months to help participants recognize hunger signals and manage binge eating. The other group participates in an attention-control program with weekly emails on wellness, binge eating, diet, and activity. Both programs focus on preventing weight gain and improving eating behaviors. Participants will be monitored for recruitment success, retention rates, and session attendance over six months. Researchers will assess changes in binge eating episodes and weight regain at three and six months. The study includes digital engagement, psychoeducation, and behavioral support, with evaluations through questionnaires and app usage. Participants must have a Bluetooth-enabled smartphone and reside or work near the study location to participate.
CONDITIONS
Brief Title
Treating Binge Eating and Obesity Digitally in Black Women
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Over 18 years of age
- Body mass index (BMI) of 30 kg/m^2 or higher
- Have and regularly use a Bluetooth-enabled smartphone
- Report at least one binge eating episode weekly
- Work or live within 30 miles of Kannapolis, NC
- Complete the screening questionnaire
You will not qualify if you...
- Currently pregnant
- In substance abuse treatment
- Involved in another weight reduction program
- Have a history of anorexia
- Are purging
- Currently in treatment for eating difficulties
- Are concurrent intravenous drug users
- Consume more than 4 alcoholic beverages per day
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (remote)
Duration - 6 months
Participants undergo a digital behavioral treatment involving Appetite Awareness Treatment and behavioral weight loss delivered remotely over Zoom.
Weekly remote sessions via Zoom and weekly psychoeducation emails
Duration - Up to 6 months after treatment start
Participants are monitored for changes in binge eating episodes and weight regain after treatment completion.
Assessments at 3 and 6 months
Trial Site Locations
Total: 1 location
1
UNC-Chapel Hill
Chapel Hill, North Carolina, United States, 27599
Actively Recruiting
Research Team
T
Tyisha Harper, MBA
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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