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Trial to Optimize Just-in-Time Adaptive Intervention for Binge Eating & Weight-related Behaviors

A Micro-Randomized Trial to Optimize Just-in-Time Adaptive Intervention for Binge Eating & Weight-related Behaviors

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06349460
Enrollment
300
Registered
2024-04-05
Start date
2024-03-21
Completion date
2026-06-16
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Binge Eating, Obesity

Brief summary

The purpose of this study is to conduct a micro-randomized trial to learn which evidence-based targets within a mobile intervention for binge eating and weight-related behaviors are most impactful for which people and in what sequence.

Interventions

BEHAVIORALFoodSteps behavioral intervention

Behavioral intervention that targets binge eating and weight-related behaviors. Each week, users are recommended or assigned one of five targets, set a relevant goal, and track their progress. If a target is recommended, the user can choose to select that target or a different target.

Sponsors

Northwestern University
Lead SponsorOTHER
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

In this micro-randomized trial, participants will have 2 consecutive, independent micro-randomizations at the time of target selection each week for 16 weeks: namely, 1 of 5 treatment targets will be randomly delivered, either as a recommended or assigned target, to each user, of equal probability per randomization.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults age 18 years or older * Obesity (BMI ≥30) * Recurrent binge eating (≥12 episodes in the past 3 months) * Interested in losing weight and reducing binge eating * Willing to use a mobile application * Has a smartphone with Internet access and capacity for calls and text messaging * Has a valid email address * Has access to a scale * Not pregnant * English-speaking

Exclusion criteria

* Diagnosis for which the study/intervention is not clinically indicated * Not currently receiving clinical services for weight management or binge eating

Design outcomes

Primary

MeasureTime frameDescription
Weekly change in binge eating1 weekChange in number of binge eating episodes

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 30, 2026