Actively Recruiting

Phase Not Applicable
Age: 18Years - 22Years
All Genders
ID06861608

A Single-session Intervention Adaptation of the Habit Framework for the Prevention of Eating Disorders

Led by Virginia Commonwealth University · Updated on 2025-08-06

160

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

V

Virginia Commonwealth University

Lead Sponsor

N

National Eating Disorders Association

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating a single-session intervention (SSI) adapted from the Habit Framework to prevent eating disorders (EDs) in young adults aged 18 to 22 years who show high levels of eating pathology. Eating disorders often emerge in early to late adolescence and can cause serious mental and physical health problems, with a high mortality rate. This trial aims to address barriers to accessing prevention and treatment programs by using an online SSI, which has shown promise in other mental health conditions. The trial is a randomized controlled study comparing a 30-minute online habit training intervention to a control supportive therapy session, also lasting 30 minutes. The habit training SSI includes psychoeducation on habit formation and eating disorders, real-life examples, common questions, and advice sharing. The control group engages in supportive therapy focused on sharing emotions through reading and writing exercises. Both interventions occur at a single timepoint. Participants will complete an online screening questionnaire including the Eating Attitudes Test (EAT-26) to assess risk. Eligible individuals then complete pre-intervention questionnaires, participate in the assigned intervention, and finish end-of-intervention questionnaires including feedback forms. Follow-up questionnaires are completed after one month. Researchers will measure eating disorder symptoms, habit strength, hope, hopelessness, and barriers to seeking treatment throughout the study and follow-up. The entire process is conducted remotely via online surveys and interventions.

CONDITIONS

Brief Title

A Single-session Intervention Adaptation of the Habit Framework for the Prevention of Eating Disorders

Who Can Participate

Age: 18Years - 22Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • EAT-26 score of 20 or higher indicating risk for an eating disorder
  • Ability to speak and understand English
  • Access to a phone, tablet, or computer
  • Age between 18 and 22 years
Not Eligible

You will not qualify if you...

  • Incorrectly completing attention checks in the survey prior to intervention
  • Incorrectly completing both anagram tasks in the survey prior to intervention
  • Completing the screening or pre-intervention surveys in an improbably fast time

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Pre-Intervention Questionnaires

Duration - Approximately 10 minutes

Participants complete pre-intervention questionnaires including demographics and symptom measures.

1 visit (online)

Single-session Intervention (SSI) or Control Activity

Duration - Approximately 30 minutes

Participants undergo a single 30-minute online session either of the habit training intervention or a matched supportive therapy control activity.

1 intervention visit (online)

End-of-Intervention Questionnaires

Duration - Approximately 5 minutes

Participants complete questionnaires including acceptability ratings and program feedback immediately after the intervention.

1 visit (online)

Follow-up Monitoring

Duration - Up to 1 month

Participants complete follow-up assessments up to one month after the intervention to monitor outcomes.

Follow-up questionnaires delivered by email

Trial Site Locations

Total: 1 location

1

Virginia Commonwealth University

Richmond, Virginia, United States, 23298

Actively Recruiting

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Research Team

C

Courtney Breiner

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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