Evaluation of an Internet-based intervention for patients with Long/Post-COVID following acute COVID-19 infection: A randomized controlled trial
Not Applicable
Recruiting
- Conditions
- U09.9Post COVID-19 condition, unspecified
- Registration Number
- DRKS00032199
- Lead Sponsor
- TU Dresden
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 134
Inclusion Criteria
fluency in German
- Long/Post-COVID diagnosis OR ongoing COVID-19 symptoms, new symptoms as a consequence of COVID-19, deterioration of a pre-existing illnes after COVID-19
- confirmation of COVID-19 diagnosis by a positive COVID-19 PCR test (self-report)
Exclusion Criteria
- current psychotic illness
- current addiction
- missing confirmation of a COVID-19 infection by a positive COVID-19 PCR test
- Functional status after Long/Post-COVID: exclusion with level 0 and 1
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Differences in quality of life between intervention- and control group at post-test. Quality of life is assessed by EQ-5D-5L.
- Secondary Outcome Measures
Name Time Method 1. Minimal Clinically Important Difference in quality of life of at least 15% of the range of the EQ-5D-5L in the intervention group. <br>2. Differences in psychological symptoms between intervention- and control group at post-test. Psychological symptoms are assessed by PHQ-D. <br>3. Acceptance, assessed by self-generated questionnaires to evaluate the single chapters and the intervention. <br>4. Target group/ range of influence, assessed by a self-generated questionnaire about sociodemographic variables. <br>5. Adherence, assessed by the number of finished chapters of the intervention.