Self-Guided Personalized Treatment for Women
- Conditions
- Disordered Eating
- Interventions
- Behavioral: Self-guided Personalized Treatment
- Registration Number
- NCT05920720
- Lead Sponsor
- University of Louisville
- Brief 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 50
- 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
- Active mania
- Active suicidality
- Active psychosis
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Self-guided Personalized Treatment Self-guided Personalized Treatment Women 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.
- Primary Outcome Measures
Name Time Method Clinical Impairment Up to 8 weeks Changes in clinical impairment will be assessed with the Clinical Impairment Assessment (CIA)
Anxiety Up to 8 weeks Changes in anxiety will be assessed with the Penn State Worry Questionnaire (PSWQ)
Depression Up to 8 weeks Changes in depression will be assessed with the Beck Depression Inventory-2 (BDI-2)
Disordered eating symptoms Up to 8 weeks Changes in disordered eating symptoms will be assessed with the Eating Disorder Examination Questionnaire-6 (EDE-Q6)
Quality of life Up to 8 weeks Changes in quality of life will be assessed with the Quality of Life Scale (QOLS)
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Eating Anxiety Treatment Laboratory and Clinic
🇺🇸Louisville, Kentucky, United States