covid 19. COVID-19, virus identified
Conditions
Interventions
Intervention 1: In the intervention group (mobile-based pulmonary rehabilitation software) after completing the questionnaires as a pre-test, a briefing session will be held by a specialist nurse on h
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Declare willingness to participate in the study by completing the informed consent form Age category 18-60 years Internet access and mobile phone to use mobile-based lung rehabilitation software Have a minimum literacy No vision or hearing problems Have the literacy to use a mobile phone to work with mobile-based lung rehabilitation software At least 21 days have elapsed since the onset of symptoms in patients with severe coronary artery disease.
Exclusion criteria
Exclusion criteria: Reluctance to participate in the study Participate in similar courses simultaneously Definitive evidence of venous and pulmonary thromboembolism Acute symptoms of Covid 19 (temperature over 38 degrees ....) Systolic blood pressure less than 90 mm Hg, diastolic blood pressure less than 60 mm Hg Systolic blood pressure above 140 mm Hg and diastole above 90 mm Hg History of heart disease class 4-2 Ischemic or hemorrhagic stroke or neurodegenerative diseases Major mental disorder according to psychiatrist (schizophrenia, paranoid disorders and major depression) Any disorder that restricts the patient's ability to move during pulmonary rehabilitation Patients with active cancer Patients receiving palliative care Absence of more than 2 sessions in pulmonary rehabilitation training programs or failure to answer the researcher's call more than 2 times a week
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality of Life. Timepoint: 6 months. Method of measurement: SF-12 Quality of Life Questionnaire, HADS Hospital Anxiety and Depression Scale, Bartel Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Stress and depression. Timepoint: 6 months. Method of measurement: Anxiety and Depression Clinical Scale Questionnaire(HADS).;Fasting days of life. Timepoint: 6 months. Method of measurement: Bartel Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactRamin Sami
Esfahan University of Medical Sciences
Outcome results
None listed