New app aims to ease anorexia recovery after hospital discharge
NCT ID NCT05499676
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study developed and tested a mobile app with coaching and a social network for adults with anorexia nervosa who recently left intensive treatment. The goal was to see if the app could help reduce eating disorder symptoms compared to usual care. 90 women participated, and the app was designed to support them during the challenging post-acute period.
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
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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
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90 people
The number who actually took part.
- Started
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Dec 2022
- Finished
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Mar 2025
- Lead sponsor
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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
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Cisgender women who are 18 years old and older, who own a mobile phone, speak English, are U.S. residents, have a BMI greater than or equal to 17, who are connected with a physician (such as a primary care provider), who are not using a feeding tube, and who have been discharged from intensive treatment (i.e., inpatient, residential, partial hospitalization, intensive outpatient) for DSM-5 anorexia nervosa within the past 2 months. Exclusion Criteria: * Individuals who are not cisgender women. * Individuals under 18 years old. * Individuals who do not own a mobile phone. * Individuals who have not been discharged from intensive treatment (i.e., inpatient, residential, partial hospitalization, intensive outpatient) for DSM-5 anorexia nervosa within the past 2 months). * Individuals who are not connected with a physician (such as a primary care provider) * Individuals who have a BMI below 17.0 * Individuals who are currently using a feeding tube
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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.
Contacts and locations
Locations
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Columbia University
New York, New York, 10032, United States
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Palo Alto University
Palo Alto, California, 94304, United States
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Washington University School of Medicine
St Louis, Missouri, 63110, United States
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Other studies related to the condition(s) this trial covers.
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