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RecruitingNCT06861608Updated Aug 5, 2026

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

An interventional study of Screening Questionnaire and Pre-Intervention Questionnaires (~10 minutes) in Eating Disorder Not Otherwise Specified, sponsored by Virginia Commonwealth University. Recruiting at 1 site in United States. Open to participants aged 18 Years to 22 Years. Per ClinicalTrials.gov, last updated 2026-08-05.

Sponsored by Virginia Commonwealth University · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Started Jan 2025; still recruiting 1 year 8 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
160
Allocation
Randomized
Ages
18 Years to 22 Years
Sex
All
01

Study summary

The purpose of this proposal is to launch the first trial of a single-session intervention (SSI) specifically for the prevention of eating disorders (EDs).

Read the detailed description

The emergence of EDs is bimodal such that there is a period of risk in early adolescence and a period of risk in late adolescence/early adulthood. EDs can lead to significant mental and physical health consequences and have one of the highest mortality rates of any mental illness. Prevention and treatment programs for EDs are fraught with barriers to access, particularly related to seeking care in-person. SSIs have been identified as a pathway to address the gap in care for EDs after showing promise for other psychiatric problems, including depression, anxiety, and suicidality .

02

Conditions studied

  • Eating Disorder Not Otherwise Specified

Keywords

  • prevention of eating disorders
03

In context

Lead sponsor

Virginia Commonwealth University is the lead sponsor of 641 studies on the registry; 82 are open to participants now.

Of its 88 completed or terminated interventional studies of FDA-regulated products, 62 (70%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 22 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • EAT-26 score ≥ 20 ( EAT-26, participants will meet the "referral criteria" which includes a score of 20 or more or meeting frequency criteria on bingeing, purging, laxative/diuretic use, and/or exercise.)
  • English-language fluency, self-reported3
  • Access to a phone, tablet, or computer

Exclusion criteria

Exclusion Criteria:

  • Failure to correctly complete one of the attention checks in the survey prior to the intervention
  • Failure to correctly complete both anagram tasks in the survey prior to the intervention
  • Completion of the screening survey or pre-intervention surveys in an improbably fast time
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
160 participants (estimated)

Study arms

  • Experimental
    Experimental: psychoeducation experience single-session intervention (SSI)

    This online randomized controlled trial of a habit training intervention includes one 30-minute session for young adults endorsing high levels of eating pathology. The intervention will occur at one timepoint.

    Behavioral: Screening Questionnaire · Behavioral: Pre-Intervention Questionnaires (~10 minutes) · Behavioral: SSI (Single-session intervention (~30 minutes) Active arm · Behavioral: End-of-Intervention Questionnaires (~5 minutes)

  • Placebo comparator
    Control: will be matched to the SSI by including both reading and writing exercises.

    The control intervention will consist of supportive therapy focusing on sharing emotions and include an introduction to emotions, writing about emotions, testimonials from other adolescents about the power of sharing emotions, and an exercise asking adolescents how different situations might make them feel.

    Behavioral: Screening Questionnaire · Behavioral: Pre-Intervention Questionnaires (~10 minutes) · Behavioral: SSI (Single-session intervention (~30 minutes) control arm · Behavioral: End-of-Intervention Questionnaires (~5 minutes)

Interventions

  • BehavioralScreening Questionnaire

    Individuals will complete an online screening survey through an online study advertisement to determine initial eligibility. The screening survey will ask participants to report their gender and age and complete the Eating Attitudes Test - 26-item (EAT-26). EAT-26 scores equal to or greater than 20 indicate risk for an eating disorder. EAT-26, participants will meet the "referral criteria" which includes a score of 20 or more or meeting frequency criteria on bingeing, purging, laxative/diuretic use, and/or exercise. If an interested individual is not eligible, they will be notified that they are not currently eligible for the study and provided with resources.

  • BehavioralPre-Intervention Questionnaires (~10 minutes)

    Eligible participants will complete pre-intervention questionnaires including demographics and symptom measures.

  • BehavioralSSI (Single-session intervention (~30 minutes) Active arm

    The SSI will consist of four components: 1)psychoeducation, 2) real-life examples, 3) common questions and misconceptions, and 4) providing advice to other young adults. Psychoeducation will focus on the brain bases of habit formation and EDs, as per REACH+ treatment manual. Participants will then be asked to think of a real-life example of an eating habit in which they have been engaged, such as limiting their intake of dessert foods. Participants will then be provided with REACH+ developed psychoeducation regarding changing habits, including information on competing responses, stimulus control, and exposure. Participants will have the opportunity to write out how they could use one of these strategies to tackle the habit that they previously wrote about. They will be provided with a worksheet to help them move through each aspect of changing their habit based on what they learned.

  • BehavioralSSI (Single-session intervention (~30 minutes) control arm

    The control condition will be matched to the SSI by including both reading and writing exercises. The control intervention will consist of supportive therapy focusing on sharing emotions and include an introduction to emotions, writing about emotions, testimonials from other adolescents about the power of sharing emotions, and an exercise asking adolescents how different situations might make them feel.

  • BehavioralEnd-of-Intervention Questionnaires (~5 minutes)

    Participants will complete additional questionnaires at the end of the intervention, including acceptability ratings and program feedback. Participants will provide an email address at the end of the questionnaires for receipt of four-week follow-up questionnaires.

06

What researchers measure

Primary outcomes

  1. Eating Attitudes Test - 26-item

    This 26-item measure will be used to assess eating disorder, including bingeing, purging, and exercise behaviors. According to this methodology, individuals who score 20 or more on the test should be interviewed by a qualified professional to determine if they meet the diagnostic criteria for an eating disorder. If you have a low score on the EAT-26 (below 20), you still could have a serious eating problem, so do not let the results deter you from seeking help. For example, some individuals with Binge Eating Disorder (BED) score low on the EAT-26 but may have a serious eating disorder.

    Time frame: Baseline though study completion and up to one month follow-up

  2. The Brief (Seven-item) Eating Disorder Examination Questionnaire

    This measure will be used to assess eating behaviors over the past month. The seven-item version consists of seven items derived from the original Eating Disorder Examination Questionnaire and assesses for dietary restraint, shape/weight overvaluation, and body dissatisfaction. It consists of three subscales: dietary restraint (items 1, 3 and 4), shape/weight overvaluation (items 22 and 23) and body dissatisfaction (items 25 and 26).

    Time frame: Baseline though study completion and up to one month follow-up

  3. Self-report Habit Index

    The self-report habit index measures habit strength, which is the underlying mechanism being targeted in the current intervention. 7-point Likert scale from "strongly disagree" to "strongly agree." Higher scores indicate a stronger habit, suggesting the behavior is more automatic and less consciously controlled.

    Time frame: Baseline though study completion and up to one month follow-up

  4. State Hope Scale - Agency Subscale

    The 3-item agency subscale of the State Hope Scale measures belief in one's capacity to initiate and sustain actions. Research has shown that high agency is predictive of goal-related activities and utilization of coping skills. Higher scores on the agency subscale generally indicate a stronger sense of personal agency and belief in one's ability to take control and actively pursue goals.

    Time frame: Baseline though study completion and up to one month follow-up

  5. Beck Hopelessness Scale - 4-item Version

    This 4-item measure assesses hopelessness about the future with excellent psychometric properties and good internal consistency. typically calculated by summing up the responses to the four selected items, with a potential range from 0 to 4, where higher scores indicate greater levels of hopelessness.

    Time frame: Baseline though study completion and up to one month follow-up

  6. Barriers to Seeking Treatment.

    Help-seeking barriers will be assessed using this 26-item measure that was created in alignment with results of a systematic review of barriers and facilitators to help-seeking in eating disorders. A high score on a barrier-to-treatment scale suggests that the individual perceives that particular factor as a significant obstacle to seeking professional help.

    Time frame: Baseline though study completion and up to one month follow-up

  7. SSI

    The SSI will consist of four components: 1)psychoeducation, 2) real-life examples, 3) common questions and misconceptions, and 4) providing advice to other young adults based on what participants learned throughout the intervention. Psychoeducation will focus on the brain bases of habit formation and EDs, as per REACH+ treatment manual. Participants will then be asked to think of a real-life example of an eating habit in which they have been engaged, such as limiting their intake of dessert foods. Participants will then be provided with REACH+ developed psychoeducation regarding changing habits, including information on competing responses, stimulus control, and exposure. Participants will have the opportunity to write out how they could use one of these strategies to tackle the habit that they previously wrote about. They will be provided with a worksheet to help them move through through each aspect of changing their habit based on what they learned.

    Time frame: Baseline though study completion and up to one month follow-up

07

Study locations

1 of 1 sites recruiting
  • Virginia Commonwealth University
    Richmond, Virginia 23298, United States
    • Courtney Breiner · Contact · breinerc@vcu.edu · 518-376-2543
    • Courtney Breiner · Principal investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 5, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06861608
Lead sponsor
Virginia Commonwealth University
Collaborators
National Eating Disorders Association
Responsible party
Sponsor
First posted
Mar 6, 2025
Start date
Jan 15, 2025
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Aug 5, 2026

Study contacts

Courtney Breiner
Contact
breinerc@vcu.edu
518-376-2543
Courtney Breiner
principal investigator · Virginia Commonwealth University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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