ightMood Intervention to reduce depression symptoms in obese adults: A randomized-controlled online intervention study
Not Applicable
- Conditions
- Obese adults with depressive symptoms
- Registration Number
- DRKS00029219
- Lead Sponsor
- VR-Universitätsklinik Essen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 128
Inclusion Criteria
Patients with a BMI = 30
-Depressive symptoms (PHQ-8 = 10)
-Adequate digital literacy
-Internet-enabled device
-Informed consent
Exclusion Criteria
-Bariatric surgery within the past year or planned within the next 6 months
-Weekly individual psychotherapy
-No private Internet access
-Regulation of a new psychopharmacists within the last 2 weeks
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Depression symptoms (CESD-R) (T0, T1, T2, T3)
- Secondary Outcome Measures
Name Time Method -Improvement in self-efficacy (GSES), quality of life (WHOQOL) and mindfulness (FFA) <br>-Reduction of eating disorder-specific symptoms (EDE-2-B; EDI-2; EDE-Q8)<br>-Reduction of Body Mass Index (BMI)<br>-Progress/development of depressive symptoms and other sec. outcomes about the measurement time points (PHQ-4; Distress) (Measure: During Treatment)<br>- satisfaction with treatment; and usability of the LightMood intervention<br>-Usage behaviour <br>-Predictors of usage behaviour<br><br>The measuring times of the measuring instruments mentioned above take place at T0, T1, T2 and T3.