Efficacy of Pulmonary Telerehabilitation in Patients with Covid-19
Not Applicable
Recruiting
- Conditions
- Covid-19.Covid-19U07.1
- Registration Number
- IRCT20220103053609N1
- Lead Sponsor
- Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
1- Patients who were diagnosed with Covid-19 and discharged from the hospital. 2- Patients who are desired to participate in the study. 3- Patients aged between 18 to 80 years. 4- Having accessibility to the Internet.
Exclusion Criteria
1- Patients who are unwilling to continue their participation in the study. 2- Having chronic diseases, such as pulmonary disease, kidney diseases, neurologic disease, high blood pressure, uncontrolled heart disease, rheumatic diseases, cognitive disorders and psychological problems, and musculoskeletal disease. 3. Patients who have undergone any physiotherapy. 4. Patients who have participated in any rehabilitation programs during the study.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Quality of life based on SF-36 score. Timepoint: Just before rehabilitation and 3 weeks later. Method of measurement: SF-36 questionnaire, Clinical Assessment, finger O2 Saturation monitor.
- Secondary Outcome Measures
Name Time Method Heart rate checked by pulse oxymeter. Timepoint: Just before intervention and 3 weaks later. Method of measurement: by pulse oxymeter.;Severity of dyspnea based on borge scale. Timepoint: Just before rehabilitation and 3 weaks later. Method of measurement: Borge scale.;Blood oxygen saturation checked by pulse oxymeter. Timepoint: Just before rehabilitation and 3 weaks later. Method of measurement: Puls oxymeter.