Telemedicine-supported Rehabilitation after COVID-19 infection (long-covid)
Not Applicable
- Conditions
- U09.9Post COVID-19 condition, unspecified
- Registration Number
- DRKS00026245
- Lead Sponsor
- Medizinische Hochschule Hannover
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 69
Inclusion Criteria
Women and men up to 6 months after Covid-19 disease (positive SARS-CoV-2 PCR or AK detection),
anamnestic existing limitation of benefits,
Fatigue Assessment Scale (FAS) (=22 points),
Age: = 18 years
Exclusion Criteria
- current participation in another intervention study
- other clinically relevant acute or chronic infections
- pregnancy
- Operations that were less than 8 weeks ago
- Illnesses or functional impairments which, based on the assessment of the examining doctor, exclude participation in a physical training intervention
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Maximum oxygen uptake (in ml/min), recorded at baseline, after 3 months intervention and after 6 months (follow up).
- Secondary Outcome Measures
Name Time Method 6 minute walk test,<br>Vascular examinations using retina analysis, pulse wave transit time,<br>Flow mediated Dilation / AngioDefender,<br>Pulmonary function measurement,<br>Hand gripping force measurement,<br>Sit to stand test, macular flow density, using optical coherence tomography,<br>Bio-impedance analysis of body composition,<br>Questionnaires: SF-36, HADS, FAS, cognition, WAI, MEDAS, 7-day nutrition protocol, WAI, self-efficacy expectation, D2 test, MOCA, BDI-2, ADNM20, residence, partnership, Brief Resilience Scale,<br>Standard laboratory values, via venous blood collection.<br>Parameters recorded at baseline, after 3, 6 and 12 months