Combining Digital Cognitive-behavior Therapy With Mindfulness Training for Binge Eating Disorder
Recruiting · NCT07212673 · Interventional (participants receive a specific treatment) · Lead sponsor: Yeshiva University
View the official record on ClinicalTrials.gov →Interventions studied
CBT-based Mindful CourageCoached Self-Monitoring
What this trial is about
The investigators will evaluate the acceptability and feasibility of a 16-session digital mindfulness-based and cognitive behavioral therapy (CBT) intervention for binge eating disorder (BED) + coached self-monitoring vs. a coached self-monitoring intervention. This study is a pilot randomized controlled trial.
Who can take part
Age range
18 Years to 70 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- age 18 years or older
- ability to speak English fluently
- meeting DSM-5 criteria for current BED (i.e., in the past three months)
- willing and able to commit to the entire study protocol
Exclusion criteria
- a BMI below 18.5
- requiring immediate treatment for medical complications
- having current anorexia or bulimia nervosa or purging behaviors within the past year
- being pregnant or breast-feeding
- experiencing other severe psychopathology or medical illness that would limit the participants' ability to comply with the demands of the current study (e.g. active suicidal risk, active psychotic disorder, unmedicated bipolar disorder, severe substance use disorder, cancer)
- currently receiving BED or weight loss treatment (treatment for other conditions will be allowed, as long as the treatment is not mindfulness-based)
- currently taking medications for weight loss, or beginning medications that affect eating/weight within the last six months.
Where it is running
1 location listed across 1 US state.
- Yeshiva University - The Bronx, New York, United States