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Can a phone app tame disordered eating? small study tests personalized Self-Help

NCT ID NCT05920720

Symptom relief Sponsor: University of Louisville Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested a self-guided smartphone program for women with disordered eating. Twenty women used their phones to track eating habits for two weeks, then received two personalized treatment modules. Researchers checked if the program was easy to use and if it helped reduce symptoms like anxiety and depression over two months.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
self-guided personalized mobile treatment modules
What this could lead to
If it works, this could offer a convenient, low-cost way for women to manage disordered eating symptoms on their own.
What could go wrong
This is a very small, early study with only 20 participants and no control group. Results may not apply to everyone, and the app may not be effective for all users.

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

20 people

The number who actually took part.

Started

Feb 2025

Finished

Mar 2026

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

Accepted

You do not need to have the condition being studied to take part.

Show 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: * Endorse disordered eating (score of 2.3 or above on EDE-Q6) * Age 18-65 * Ability to read and write English * Own a smartphone or tablet Exclusion Criteria: * Active mania * Active suicidality * Active psychosis

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Conditions

The condition(s) this trial relates to.

anorexia nervosa Binge-Eating Disorder bulimia nervosa eating disorder Feeding and Eating Disorders

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Disordered eating

Contacts and locations

Locations

  • Eating Anxiety Treatment Laboratory and Clinic

    Louisville, Kentucky, 40205-1016, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.