Self-Guided Personalized Treatment for Women

Status Not yet recruiting

Clinical Trial Summary

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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Disordered Eating

Clinical Trial Details

NCT number	NCT05920720
Study type	Interventional
Source	University of Louisville
Contact	Cheri A Levinson, PhD
Phone	502-852-7710
Email	cheri.levinson@louisville.edu
Status	Not yet recruiting
Phase	N/A
Start date	July 1, 2024
Completion date	March 15, 2025

View Details

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