Could your phone help rewire binge-eating habits?
NCT ID NCT05473013
First seen Aug 19, 2026 · Last updated Sep 11, 2026 · Updated 2 times
Summary
This study tests whether adding smartphone-based self-monitoring and micro-interventions to standard behavioral therapy helps people with bulimia nervosa or binge eating disorder. Participants will use an app to track their eating and practice therapeutic skills, with some receiving more complex monitoring and prompts. The goal is to see which combination works best for reducing binge eating and improving overall eating habits.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Behavioral therapy for eating disorders combined with smartphone-based self-monitoring and micro-interventions
- What this could lead to
- If successful, this could point toward more effective, personalized digital tools to help people with binge eating disorders learn and use coping skills, potentially improving treatment outcomes.
- What could go wrong
- This is an early-stage trial, and the added digital components may not improve outcomes beyond standard therapy. Results may also vary depending on individual self-regulation skills.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 264 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Jan 2023
- Expected to finish
-
Jan 2027
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Are 18 to 65 years old. 2. Have experienced 12 or more loss of control episodes within the previous 3 months. 3. Have a BMI above 18.5. 4. Are located in the US and willing/able to participate in remote treatment and assessments. 5. Have a smartphone. 6. Complete the three-day app trial after the baseline assessment (i.e., the participant shows that they can self-monitor their episodes of eating three times a day for three days). Exclusion Criteria: 1. Are unable to fluently speak, write and read English. 2. Have a BMI below 18.5. 3. Are already receiving treatment for an eating disorder (e.g., research participants cannot be receiving concurrent eating disorder treatment in the clinical trial and from another provider). Participants willing to pause their existing eating disorder treatment for the duration of the clinical trial are eligible to participate. 4. Are already receiving pharmacological or behavioral treatment for weight loss. 5. If they meet the criteria for PCP clearance (see "Primary care physician clearance" section above) and are not deemed safe for outpatient treatment by a primary care physician. 6. If they meet the criteria for PCP clearance and are unwilling to receive medical clearance and/or medical monitoring as requested by the study to ensure they are medically safe to participate. 7. Have a mental handicap or are experiencing other severe psychopathology that would limit the research participants' ability to comply with the demands of the current study (e.g., imminent suicide risk, active psychotic disorder). Imminent suicide risk is assessed through the C-SSRS and a full risk assessment (see "Plan for assessing and/or intervening on suicidal ideation" above). Active psychotic disorder is assessed during the phone screen and with the standardized assessment checklist. 8. Are using a substance wherein the substance use is creating significant functional impairment that it is unlikely they can safely and effectively participate in an outpatient treatment study for eating pathology (i.e., the substance use: is interfering with day-to-day responsibilities and/or has gotten them in trouble with the law in the past year and/or has prevented them from attending/completing work and/or school within the past year) and/or if they are experiencing medical symptoms related to their substance use that requires immediate treatment and/or are unwilling or refrain from using the substances when it may interfere with treatment sessions and assessments (i.e., unwilling to not use the substances starting 2 hours prior to assessments and treatment sessions). Substance use is assessed during the phone screen and with the standardized assessment checklist. 9. Are pregnant or planning to become pregnant within the next year and a half.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Binge eating are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Nemours Children's Health, Wilmington
RECRUITINGWilmington, Delaware, 19803, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- A digital coach for hunger: can an app retrain appetite to improve diabetes control?
- A new approach to curb binge eating may lower diabetes risk in young black women
- Can video therapy match In-Person care for bulimia?
- Digital coaching may curb binge eating in black women with obesity
- Do diaries differ? study tests paper vs. digital for binge eating tracking
- Which talk therapy works best for binge eating? a Head-to-Head trial aims to find out