The effect of pulmonary rehabilitation Mobile base applicatio

Not Applicable

Recruiting

Conditions: covid 19.
COVID-19, virus identified
U07.1

Registration Number: IRCT20200411047029N2

Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: All

Target Recruitment: 38

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

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

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Quality of Life. Timepoint: 6 months. Method of measurement: SF-12 Quality of Life Questionnaire, HADS Hospital Anxiety and Depression Scale, Bartel Scale.

Secondary Outcome Measures

Name	Time	Method
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.