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Completed

NCT Number: NCT06107387

Binge Eating Self-help for Teens ONLINE Pilot and Feasibility Study

This study is a pilot clinical trial of a new guided self-help CBT for binge eating. Participants will complete an intake assessment; following determination of eligibility, participants will then complete four months of treatment (weekly guided self-help sessions). At the end of treatment, participants will complete an interview with a research clinician to assess outcomes.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

To be included, adolescents must:

  • Be in the age range ≥12 years old and ≤17 years old;
  • Have a BMI that places them above the 85th percentile based on their age and sex;
  • Report 2 episodes of binge/LOC eating (feeling a loss of control while eating) per month for the past 3 months;
  • Be otherwise-healthy youth (i.e., no uncontrolled or serious medical conditions);
  • Read, comprehend, and write English at a sufficient level to complete study-related materials;
  • Provide a signed and dated written assent prior to study participation;
  • Provide a signed and dated written consent from one parent prior to study participant; and
  • Be available for participation in the study for 4 months.

Exclusion criteria

Prospective participants will be excluded if the adolescent:

  • Has a medical or psychiatric condition that would require hospitalization or intensive care (e.g., neurological disorder, psychotic disorders, suicidality);
  • Has a medical or psychiatric condition that would prohibit them from engaging in behavioral treatment or moderate physical activity (e.g., cardiovascular problems);
  • Has uncontrolled medical condition(s) (e.g., uncontrolled diabetes or hypertension);
  • Is pregnant or breastfeeding;
  • Is taking medication(s) or participating in treatment(s) that could influence weight or appetite;
  • Began taking hormonal contraceptives less than 3 months prior;
  • Has a developmental or cognitive disorder (e.g., autism spectrum disorder);
  • Has a concurrent feeding/eating disorder (e.g., bulimia nervosa); or
  • Is participating in another clinical research study.

Treatment and study plan

Binge Eating Self-help for Teens

Behavioral

Guided self-help intervention

Other names: BEST

Primary outcomes

  1. Attendance

    Time frame: 4 months

    Number of participants attending >75% of sessions

  2. Retention

    Time frame: 4 months

    Number of participants who attend through the end of treatment

Secondary outcomes

  1. Treatment Credibility

    Time frame: 1 week

    Adolescent/parent treatment credibility (moderate or higher, study-specific face-valid treatment credibility form)

  2. Treatment Satisfaction

    Time frame: 4 months

    Adolescent/parent/clinician treatment satisfaction (acceptable or higher, Client Satisfaction Questionnaire)

Sponsors and collaborators

Lead sponsor

Yale University

Other

Registry information

Official study title

Binge Eating Self-help for Teens (BEST): A Pilot and Feasibility Test of an Online Behavioral Intervention for Adolescents With Binge Eating and Elevated Weight

Acronym: BEST

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Oct 30, 2023
Registry last updated
Dec 4, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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