Clinical Effects of Internet Assisted Pulmonary Rehabilitation of COVID-2019 Pneumonia Patients After Discharge
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|ClinicalTrials.gov Identifier: NCT04368793|
Recruitment Status : Recruiting
First Posted : April 30, 2020
Last Update Posted : July 17, 2020
|Condition or disease||Intervention/treatment|
|COVID-2019 Pneumonia Pulmonary Rehabilitation||Behavioral: Remote pulmonary rehabilitation|
|Study Type :||Observational|
|Estimated Enrollment :||200 participants|
|Official Title:||Intelligence-based Remote Pulmonary Rehabilitation and Efficacy Among Discharged COVID-19 Patients|
|Actual Study Start Date :||April 6, 2020|
|Estimated Primary Completion Date :||December 31, 2020|
|Estimated Study Completion Date :||December 31, 2021|
Discharged COVID-19 patient cohort
All enrolled participants will be given 8 weeks (online 2 weeks + offline 6 weeks) pulmonary rehabilitation intervention, and will be followed up for at least one year, to assess their adherence and efficacy of the rehabilitation program.
Behavioral: Remote pulmonary rehabilitation
The pulmonary rehabilitation intervention includes respiratory exercise, barehanded aerobic training, exercise prescription of elastic band impedance training, respiratory muscle strength training, etc.
- Six-minute walking distance (6MWD) [ Time Frame: One year ]Walking distance within six minutes
- Pulmonary function [ Time Frame: One year ]Forced expiratory volume in one second (FEV1), forced vital capacity (FVC), etc.
- Respiratory muscle strength [ Time Frame: One year ]Maximal inspiratory pressure, maximal expiratory pressure, etc.
- Physical fitness assessment [ Time Frame: One year ]Two-minute walking test, short physical performance battery, grip strength of both upper limbs, knee extension strength of both lower limbs, etc.
- Symptom [ Time Frame: One year ]Modified British Medical Research Council (mMRC) dyspnea scale, etc.
- Psychological evaluation [ Time Frame: One year ]Self-training depression scale (SDS) and self-rating anxiety scale (SAS)
- Quality of life [ Time Frame: One year ]36-item short-form health survey (SF-36), etc.
- Physical activity [ Time Frame: One year ]International physical activity questionnaire (IPAQ)
- Proportion of returning to society [ Time Frame: One year ]Proportions of returning to routine work and normal life
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04368793
|Contact: Geyi Wen, Resident||+86 email@example.com|
|Contact: Lulu Yang, Resident||+86 firstname.lastname@example.org|
|Wuhan Lung Hospital||Recruiting|
|Wuhan, Hubei, China, 100191|
|Contact: Guangyun Guo, Doctor +86 13886806423|
|Wuhan Central Hospital||Recruiting|
|Wuhan, Hubei, China, 430014|
|Contact: Yi Hu, Doctor +86 13995618974|
|Zhongnan Hospital of Wuhan University||Recruiting|
|Wuhan, Hubei, China, 430071|
|Contact: Zhenshun Cheng, Doctor +86 13627288300|
|Principal Investigator:||Ting Yang, Prof.||China-Japan Friendship Hospital|