Evaluation of an Internet-based intervention for patients with Long/Post-COVID following acute COVID-19 infection: A Cohort Study
Not Applicable
Recruiting
- Conditions
- U09.9Post COVID-19 condition, unspecified
- Registration Number
- DRKS00032668
- Lead Sponsor
- TU Dresden
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
legal age
- fluent in german
- written confirmation of the Long/Post-COVID diagnosis by a doctor
- informed consent to take part in our first epidemiological study about Long/Post-COVID (SR+BO-67022023)
Exclusion Criteria
- underage
- current psychotic disorder
- current addiction disorder
- functional status after Long/Post-COVID below 2
- missing confirmation of the Long/Post-COVID diagnosis by a doctor
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Differences in quality of life (EQ-5D-5L) between pre- and post-test.
- Secondary Outcome Measures
Name Time Method 1. Differences in psychological symptoms (PHQ-D) between pre- and post-test.<br>2. Minimally Clinically Important Difference in quality of life of at least 15% of the range of the EQ-5D-5L. <br>3. Minimally Clinically Important Difference in psychological symptoms of at least 15% of the subscales of the PHQ-D. <br>4. Acceptance, assessed by self-generated questionnaires to evaluate the single chapters and the intervention. <br>5. Target group/ range of influence, assessed by a self-generated questionnaire about sociodemographic variables. <br>6. Adherence, assessed by the number of finished chapters of the intervention.