Self-Guided Personalized Treatment for Women

Completed · Not applicable

Conditions studied: Disordered Eating

In brief

The investigators plan to collect preliminary data on the feasibility, acceptability, and user uptake of a personalized self-guided mobile intervention for disordered eating (DE) and test the initial clinical efficacy of this intervention. Women (N=50) who endorse significant DE will complete two weeks of smart-phone self-monitoring to identify target problems and will be sent two self-guided modules of personalized treatment directly to their smart-phones. The investigators will assess engagement with the modules throughout two months and administer baseline, week 5, and week 8 assessments for acceptability, uptake, and initial clinical efficacy (e.g., DE symptoms, anxiety, quality of life). The investigators will also complete a focus group (n=10) with a subset of users to receive input on the mobile-application assessment and ease of self-guided intervention modules.

Key facts

Study ID

NCT05920720

Run by

University of Louisville

People needed

20

Starts

2025-02-28

Expected to finish

2026-03-06

Last updated by the study team

2026-05-04

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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

You may not qualify if…

• Active mania
• Active suicidality
• Active psychosis

Where it is running

• Eating Anxiety Treatment Laboratory and Clinic — Louisville, Kentucky, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.