Addressing psycho-social needs in patients with Long-Covid - a pilot study
Not Applicable
- Conditions
- ong-Covid, Post-CovidU09.9!
- Registration Number
- DRKS00030866
- Lead Sponsor
- Klinikum rechts der Isar der TU München
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 123
Inclusion Criteria
• Previous COVID-19-infection (at least 4 weeks ago)
• At least one symptom of Long-COVID
• Written consent
• Suitable place of residence to attend the appointments at one of the locations
• Availability during intervention period
Exclusion Criteria
• Severe psychiatric illness according to ICD-10 (F0, F1, F2, F31)
• Suicidality
• Currently receiving psychotherapeutic treatment or having received psychotherapeutic treatment for Long-COVID
• Insufficient German language skills
• Lack of capacity to give consent
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improvement of (health-related) quality of life as measured by self-reported questionnaires (SF-12)<br>The SF-12 will be completed before starting with the therapeutic intervention (t1), after completing the last therapy session (t2) and 3 months after ending the intervention (t3)
- Secondary Outcome Measures
Name Time Method Via self-reported questionnaired:<br>• Improvement/changes of somatic symptoms as well as other Long-COVID-related symptoms like fatigue, stress, symptoms of depression or anxiety (at t1, t2 and t3)<br>• Improvement/changes of ability to work or fulfill daily demands; beliefs and feelings about the illness (at t1, t2 and t3)<br>• Satisfaction with the intervention (at t2 and t3)<br>Via blood collection<br>• Cytokine profiling and possible changes