Combining Digital Cognitive-behavior Therapy With Mindfulness Training for Binge Eating Disorder
Combining Digital Cognitive-behavior Therapy With Mindfulness Training for Binge Eating Disorder: a Feasibility Randomized Controlled Trial
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 18 Years to 70 Years
- Sex
- All sexes
- Healthy volunteers
- Not accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
Not stated in the study description — ask the study team about visits and procedures.
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
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.
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Official eligibility criteria
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.
Study sites (1)
NY
- Yeshiva University · The Bronx, NY 10461Margaret Sala · Study contact · 972-369-4267 · margarita.sala@yu.eduMore trials in The Bronx