COVID-19. COVID-19, virus identified
Conditions
Interventions
Intervention 1: Intervention group: pulmonary telerehabilition with progressive muscle relaxation exercise. pulmonary rehabilitation includes breathing exercises, aerobic and resistance exercises. The
Sponsors
Iran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: COVID-19 confirmed with polymerase chain reaction test (PCR) Discharged from hospital (at least six days after the onset of symptoms) Patients who have to the ability to read and write in Persian Patients who access to the Internet and video call service
Exclusion criteria
Exclusion criteria: Severe heart condition such as uncontrolled arrhythmias Chronic pulmonary and kidney condition Severe neurological condition such as guillan-barre, stroke and multiple sclerosis Uncontrolled diabetes or hypertension Smoker Athlete Pregnant women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Exercise capacity. Timepoint: before intervention, up to two and six week after intervention. Method of measurement: Six minute walk test. | — |
Secondary
| Measure | Time frame |
|---|---|
| Dyspnea. Timepoint: Before intervention, up to two and six week after start of intervention. Method of measurement: 0-10 dyspnea Borg scale.;Axiety. Timepoint: Before intervention and six weeks after start of intervention. Method of measurement: Hospital anxiety and depression scale.;Sleep quality. Timepoint: Before intervention, six weeks after start of intervention. Method of measurement: Petersborg sleep quality questionaire.;Quality of life. Timepoint: Before intervention, six weeks after start of intervention. Method of measurement: SF36, santgeorg respiratory questionaire.;Fatigue severity. Timepoint: Before intervention, six weeks after start of intervention. Method of measurement: fatigue severity scale.;Exercise capacity. Timepoint: Before intervention, six weeks after start of intervention. Method of measurement: repeated chair rise test during 30 seconds.;Depression. Timepoint: Before intervention and six weeks after start of intervention. Method of measurement: Hospital anxiety and depression scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactJavad Sarrafzadeh
Iran University of Medical Sciences
Outcome results
None listed