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Not yet recruitingNCT06326099Updated Mar 10, 2025

Brief Binge Eating and Drinking Online Intervention

An interventional study of Brief Online Binge Eating and Drinking Intervention in Binge Eating and Binge Drinking, sponsored by University of Southern California. Not yet recruiting. Open to participants aged 18 Years to 24 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-03-10.

Sponsored by University of Southern California · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Apr 2026, 6 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
300
Allocation
Randomized
Ages
18 Years to 24 Years
Sex
All
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Study summary

This pilot project targets both binge drinking and binge eating behavior in college students through a mobile-based online program that provides students with evidence-based intervention material designed to reduce the incidence of both behaviors and encourage students to seek more formal in-person counseling.

Read the detailed description

Despite the prevalence of binge drinking and binge eating behaviors among college students, few students seek care for either. Intervening with college students early is essential as untreated symptoms of binge drinking and binge eating behaviors can become more severe and persistent over time, often leading to diagnosed disorders and lasting consequences on students' social functioning, physical health, and educational attainment. Thus, the major goal of this research study is to target both binge drinking and binge eating behavior in college students through a mobile-based online program that provides students with evidence-based intervention material designed to reduce the incidence of both behaviors, as well as encourage students to seek more formal in-person counseling. The intervention combines two innovations to facilitate behavior change: (1) personalized drinking and binge eating intervention content with harm reduction and cognitive behavioral skills proven to be efficacious in reducing these problematic behaviors among college students delivered via (2) a mobile-based program that increases accessibility, is easy and engaging to use, and broadens the accessibility of the intervention content to an often non-treatment seeking group. The intervention is informed by evidence-based practices, with student and expert feedback, to help limit alcohol consumption, engage in healthier eating behaviors, and practice alternate strategies to manage negative affect.

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Conditions studied

  • Binge Eating
  • Binge Drinking
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In context

Bulimia

173 studies on the registry are indexed under Bulimia; 33 are open to participants now.

This study's planned enrollment of 300 is above the median of 60 across 143 interventional studies indexed under Bulimia.

Browse Bulimia studies →

Lead sponsor

University of Southern California is the lead sponsor of 791 studies on the registry; 136 are open to participants now.

Of its 70 completed or terminated interventional studies of FDA-regulated products, 32 (46%) have results posted.

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

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Who can participate

Ages eligible
18 Years to 24 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • full time undergraduate student at the study site
  • between the ages of 18 and 24
  • ability to speak and read English
  • at least two occasions of binge drinking (5 or more drinks in a row for males, 4 (i.e., an objectively large amount of food with a self-reported loss of control) in the past 28 days
  • at least two occasions of binge eating (i.e., an objectively large amount of food with a self-reported loss of control)151 in the past 28 days
  • no receipt of mental health or substance use care in the past month.

Exclusion criteria

Exclusion Criteria:

  • not meeting eligibility criteria
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
300 participants (estimated)

Study arms

  • Experimental
    Brief Online Binge Eating and Drinking Intervention

    The intervention is a 30 minute mobile phone program designed to address binge eating and drinking. The program addresses underlying loss of control, impulsivity, and emotion regulation common to both binge drinking and binge eating through videos, interactive activities, and psychoeducation.

    Behavioral: Brief Online Binge Eating and Drinking Intervention

  • No intervention
    Resources Only

    Campus-specific resources for how to access the university's counseling office (i.e., student mental health services), information about the Eating Disorders program at the university, and information on accessing the university's alcohol and drug awareness offices.

Interventions

  • BehavioralBrief Online Binge Eating and Drinking Intervention

    The intervention is an online mobile phone program developed by our research team. It builds upon efficacious brief alcohol interventions with college students by addressing underlying loss of control, impulsivity, and emotion regulation through the use of videos, interactive activities, and psychoeducation.

    Also known as: Sip n' Savor

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What researchers measure

Primary outcomes

  1. Frequency of past 28-day binge drinking

    Number of binge drinking episodes in the past 28 days

    Time frame: Baseline, one-month follow-up, and three-month follow-up

  2. Frequency of past 28-day binge eating

    Number of binge eating episodes in the past 28 days

    Time frame: Baseline, one-month follow-up, and three-month follow-up

  3. Brief Young Adult Alcohol Consequences Questionnaire (B-YAACQ)

    21 alcohol-related consequences experienced in the past month. Sum positive responses to get a score from 0 to 24 (higher score indicates greater number of consequences)

    Time frame: Baseline, one-month follow-up, and three-month follow-up

Secondary outcomes

  1. Mental Health/Substance Use Disorder Treatment History Inventory

    Utilization of mental health and/or substance use care

    Time frame: Baseline, one-month follow-up, and three-month follow-up

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: Yes — Following the NIH Data Sharing Policy and Implementation Guidelines, we plan to make the datasets available for sharing at the time that the main project findings are accepted for publication during the final year of the project.

Supporting information: Study protocol

Time frame: Within one year of the main effects paper being submitted for publication

Access criteria: Individual researchers can contact the PIs for data and through filling out a data request and use form that we will create for the purposes of data sharing.

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 Mar 10, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06326099
Responsible party
Eric Pedersen (Associate Professor, University of Southern California) — Principal investigator
First posted
Mar 22, 2024
Start date
May 1, 2025 (estimated)
Primary completion
Apr 30, 2026 (estimated)
Completion
Apr 30, 2026 (estimated)
Last update
Mar 10, 2025

Study contacts

Eric Pedersen, Ph.D.
Contact
Eric.Pedersen@med.usc.edu
323-442-4046

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

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