- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07521072
Testing an Intervention for College Students With Food Insecurity and Binge Eating
April 2, 2026 updated by: Heather Davis, Virginia Polytechnic Institute and State University
Building an Intervention for College Students With Food Insecurity and Binge Eating
This study is being conducted to test a new intervention.
We are interested in whether it is easy to use and complete and whether you find it helpful in reducing concerns about your eating.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
10
Phase
- Early Phase 1
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- college student status, ages 18-30 years, current food insecurity, current binge eating, and interest in changing binge eating behaviors. Food security status will be determined by 2-item the Hunger Vital Sign screening, which demonstrates high sensitivity and specificity in identifying individuals with food insecurity; scores must report mild or greater food insecurity to participate. Binge eating and related impairment will be evaluated by the Eating Disorder Diagnostic Scale and the Clinical Impairment Assessment, and the binge eating items from the Eating Disorder Examination interview. Eating behaviors must be consistent with a DSM-5-TR binge spectrum eating disorder diagnosis, whereby an individual reports binge eating episodes at minimum one time per week for the current month and at least two times per month for the prior two months, to participate. Participants will be permitted to report other mild level symptoms of psychopathology due to the high comorbidity between anxiety, depression, and binge eating among individuals with food insecurity.
Exclusion Criteria:
- Severe levels of anxiety and depression symptoms.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Binge eating intervention
This arm will test a novel binge eating intervention for college students experiencing food insecurity.
|
this intervention uses aspects of cognitive behavorial therapy for eating disorders combined with compassion-focused therapy techniques.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-Compassion Scale (SCS)
Time Frame: 3 weeks
|
SCS is a 26-item survey that measures how an individual perceives themselves, and whether they respond with self-criticism or self-compassion in times of suffering, failure, and perceived inadequacy.
|
3 weeks
|
|
Experiences of Shame Scale (ESS)
Time Frame: 3 weeks
|
The ESS is a 25-item survey that assesses an individual's perceived feelings of shame about themselves, their behaviors, and their body weight and shape; higher scores indicate greater feelings of shame.
|
3 weeks
|
|
Systems Usability Scale (SUS)
Time Frame: 3 weeks
|
Measures usability of an intervention
|
3 weeks
|
|
Digital Behavioral Change Interventions (DBCI) Engagement Scale
Time Frame: 3 weeks
|
Measures intervention engagement
|
3 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
December 1, 2026
Primary Completion (Estimated)
December 1, 2027
Study Completion (Estimated)
May 1, 2028
Study Registration Dates
First Submitted
April 2, 2026
First Submitted That Met QC Criteria
April 2, 2026
First Posted (Actual)
April 9, 2026
Study Record Updates
Last Update Posted (Actual)
April 9, 2026
Last Update Submitted That Met QC Criteria
April 2, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PK2RNLRK
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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