Treating Binge Eating and Obesity Digitally in Black Women
Binge Eating, Binge-Eating Disorder, Weight Gain Prevention
About this trial
This is an interventional screening trial for Binge Eating
Eligibility Criteria
Inclusion Criteria: Over 18 years of age, BMI ≥ 30 kg/m^2, 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 Exclusion Criteria: 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 >4 alcoholic beverages/day
Sites / Locations
- UNC-Chapel Hill
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Centering Appetite Intervention, Then Attention- Control Group
Attention- Control Group, Then Centering Appetite Intervention
Participants randomized to the attention-control group will participate remotely via a smartphone app and online lessons. The intervention will build participants' self-efficacy to reduce binge eating and to assist them in preventing weight gain.
Participants randomized to the centering appetite intervention group will receive weekly psychoeducation emails about general wellness topics, discussion of binge eating, diet, and physical activity.