Combining Digital Cognitive-behavior Therapy With Mindfulness Training for Binge Eating Disorder

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorYeshiva University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

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

Trial design

Design model

Parallel

Treatments tested in this trial

  • CBT-based Mindful Courage

    Behavioral

    Self-guided online intervention

  • Coached Self-Monitoring

    Behavioral

    Participants will log meals in recovery record

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: CBT-based Mindful Courage + Coached Self-MonitoringExperimental treatment 2 interventions
Group B: Coached Self-MonitoringActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Feasibility / Completion (questionnaire developed by our lab)

Number of participants completing intervention

Time frame
From baseline to 2-month follow-up visit
2

Acceptability

Dimensions of usability from the System Usability Scale; single-items measuring dimensions of acceptability, including overall satisfaction, engagement, visual appeal of content, understandability of program content, desire to continue the program, perceived skill acquisition, perceived confidence in implementing skills, and perceived helpfulness. Scores for each item range from 1 to 5, with higher scores indicating better acceptability. Scores will be averaged to obtain acceptability ratings.

Time frame
After completing intervention, an average of 18-weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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Yeshiva University

Lead sponsor

National Center for Complementary and Integrative Health (NCCIH)

Collaborator