An experience sampling method (ESM) app for the treatment of binge eating disorder:A proof-of-concept study
- Conditions
- binge eating disorder10014067binge eating
- Registration Number
- NL-OMON52344
- Lead Sponsor
- Erasmus Universiteit Rotterdam
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 20
In order to be eligible to participate in this study, a subject must meet be an
adult aged 18 to 65 years old, known to have binge eating disorder according to
the DSM 5 classification and who are indicated to be treated with group
therapy.
A potential subject who meets any of the following criteria will be excluded
from participation in this study:
1. Inability to understand Dutch, inability to read or write Dutch
2. No internet access or no email or no cell phone.
3. Patients who do not fill out their baseline questionnaires
4. People who use medication that is known to trigger binges, such as
corticosteroids, antipsychotics and some antidepressants (e.g. mirtazapine) or
antihistamines (e.g. promethazine).
5. People who are suspected to have a monogenetic pathology as the cause of
their obesity and binges.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p> Aim 1: Qualitative evaluations of the practical use and added value of the app<br /><br>for treatment. Aim 2: Within-person mean-level changes in emotions and<br /><br>situations and its bi-directional associations with binge eating episodes and<br /><br>cravings will be examined with the data collected with the ESM application. </p><br>
- Secondary Outcome Measures
Name Time Method <p>Not applicable. </p><br>