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Binge EatingSHAPENCT07217847

Testing SHAPE: A Single-Session Intervention Targeting Binge Eating in Women Through Assessment and Values-Based Strategies

A study testing Assessment-only and values-based reflection and goal-setting/action-planning exercises in people with Binge Eating and Binge Eating Behaviour, run by Taylor Rezeppa at 1 site in United States.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The goal of this controlled trial is to learn whether a brief single-session intervention (SSI) can reduce binge eating symptoms by targeting overvaluation of weight/shape in women with recurrent binge eating. Read more about this study

Who is it for?
Ages 18 years and older, women only
What is being tested?
Assessment-only and values-based reflection and goal-setting/action-planning exercises
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
56 participants
Where
1 siteUnited States
Study dates
Oct 2025to May 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • ≥ 18 years old
  • Identify as cisgender female
  • self-reported BMI ≥ 18.5 kg/m²
  • Rate the extent to which their weight or shape influences how they feel about themselves as a "4" or higher on a 7-point Likert scale on screening measures
  • ≥1 binge eating episode every 2 weeks (i.e., ≥ six episodes over 3 months) at the time of screening

Who cannot join

  • < 18 years old
  • Assigned male at birth
  • Gender identity different from biological sex indicated on birth certificate
  • Purging behaviors (i.e., self-induced vomiting, laxative misuse, or diuretic misuse) ≥ 1x/week in the last 3 months at the time of screening.
  • Engaged in structured psychological therapy or counseling (defined as attending sessions > 1x/month in the past 3 months)
  • Prior participation in studies that include administration of the EDE interview at Ohio University (IRB-FY24-403, IRB-FY25-330, and IRB-21-F-14).

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Taylor L Rezeppa, Master of Science contact

301-957-5805

tr036720@ohio.edu

United States1 site
  • Ohio University

    Athens, Ohio, 45705

    Taylor L Rezeppa, M.S., 3019575805, tr036720@ohio.edu

    Katherine J. Forney, Ph.D., forney@ohio.edu

Other trials in United States

About this study

Official title: Testing a Single-session Consultation for Reducing Binge Eating

The goal of this controlled trial is to learn whether a brief single-session intervention (SSI) can reduce binge eating symptoms by targeting overvaluation of weight/shape in women with recurrent binge eating.

The main questions it aims to answer are:

Read more
  • Does assessment alone reduce binge eating severity and overvaluation of weight/shape compared to a control group undergoing minimal assessment?
  • Does adding a values-based reflection and goal-setting component (the full SHAPE intervention) add benefits beyond the assessment alone?

Researchers will compare three groups:

  1. assessment-only,
  2. full SHAPE intervention, and
  3. minimal assessment control to see if both active conditions outperform the control, and whether the full intervention adds any benefits beyond the assessment itself

Participants will:

  • Complete a semi-structured eating disorder assessment (Eating Disorder Examination)
  • Depending on assignment, also complete a values-based reflection and goal-setting exercise with psychoeducation
  • Complete follow-up assessments evaluating binge eating severity, overvaluation of weight/shape, clinical impairment, binge frequency, and related outcomes.
Being tested
Assessment-only, values-based reflection and goal-setting/action-planning exercises, Minimal-Assessment Control
Keywords
single session, single-session consultation, single-session intervention, binge eating, disordered eating, binge-spectrum disorder, body image, body image concerns, weight/shape concerns, overvaluation, loss of control eating
Medical subject headings
Bulimia, Binge-Eating Disorder, Body Weight

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Assessment-onlyBehavioural

    Diagnostic items of the Eating Disorder Examindation (EDE)

  • values-based reflection and goal-setting/action-planning exercisesBehavioural

    Also called SHAPE

    Assessment-only intervention + values-based reflection and goal-setting/action-planning exercises

  • Minimal-Assessment ControlBehavioural

    Invovles completing only the Intro/Eating Pattern + Bulimic Episodes/Overeating Sections of Eating Disorder Examination (EDE)

Study groups in NCT07217847
Study groupRoleWhat they receive
Assessment-onlyActive comparatorDiagnostic items of the Eating Disorder Examindation (EDE)
Receives: Behavioral: Assessment-only
Full Intervention (SHAPE)Active comparatorDiagnostic items of the Eating Disorder Examindation (EDE) + Values-based reflection and goal-setting exercises
Receives: Behavioral: Assessment-only; Behavioral: values-based reflection and goal-setting/action-planning exercises
Minimal-Assessment ControlPlacebo comparatorIntro/Eating Pattern + Bulimic Episodes/Overeating Sections of Eating Disorder Examindation (EDE)
Receives: Behavioral: Minimal-Assessment Control

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Changes in overvaluation of weight/shape

    Changes in Shape/weight overvaluation subscale score on 7-Item Eating Disorder Examination Questionnaire

    Measured: 1 month

  2. Change in binge eating severity

    Change in scores on Binge Eating Scale

    Measured: 1 month

Secondary outcomes (6)
  1. Change in Body Image Flexibility

    5-item Body Image Acceptance and Action Questionnaire

    Measured: 1 month

  2. Change in eating self-efficacy

    Score change on Eating Self-Efficacy Brief Scale

    Measured: 1 month

  3. Change in readiness to change eating disorder symptoms

    Change in Eating Disorder Readiness Ruler scores

    Measured: 1 month

  4. Change in eating disorder-related clinical impairment

    Score change on Clinical Impairment Assessment

    Measured: 1 month

  5. Change in depressive symtpoms

    Change in Patient Health Questionnaire-8 scores

    Measured: 1 month

  6. Change in binge eating frequency

    Change in binge episode count on Eating Disorder Examination Questionnaire

    Measured: 1 month

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Oct 2025
  2. Study startOct 2025 (estimated)
  3. Primary completionOct 2026 (estimated)
  4. Study completionMay 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Factorial
Masking
Single blind
Who is masked
Participant
Enrolment
56 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07217847
Sponsor's protocol ID
IRB-FY26-100
Acronym
SHAPE
Status last verified
Oct 2025
First submitted
14 Oct 2025
Last updated
20 Oct 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Assessment-only and values-based reflection and goal-setting/action-planning exercises in people with Binge Eating and Binge Eating Behaviour, run by Taylor Rezeppa at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 20 Oct 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Taylor L Rezeppa, Master of Science (301-957-5805, tr036720@ohio.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Changes in overvaluation of weight/shape (time frame: 1 month). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Oct 2025.

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