51. Acupressure therapy and Liu Zi Jue Qigong for pulmonary function and quality of life in patients with severe novel coronavirus pneumonia (COVID-19): a study protocol for a randomized controlled trial
- Author
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Fang Min, Zhu Qingguang, Xiao Mingfang, Wei Cheng, Lei Fang, Shuaipan Zhang, and Chao Zhan
- Subjects
Complementary Therapies ,medicine.medical_specialty ,medicine.medical_treatment ,Pneumonia, Viral ,Medicine (miscellaneous) ,Acupressure ,Traditional Chinese medicine ,Patient Health Questionnaire ,law.invention ,03 medical and health sciences ,Study Protocol ,Betacoronavirus ,0302 clinical medicine ,Quality of life ,Randomized controlled trial ,law ,Acupressure therapy ,Activities of Daily Living ,medicine ,Acupressure Therapy ,Humans ,Pharmacology (medical) ,030212 general & internal medicine ,Medicine, Chinese Traditional ,Pandemics ,lcsh:R5-920 ,Rehabilitation ,business.industry ,SARS-CoV-2 ,Qigong ,COVID-19 ,Guideline ,Clinical trial ,Dyspnea ,Physical therapy ,Quality of Life ,Liu Zi Jue Qigong ,Traditional Chinese medicine rehabilitation ,business ,lcsh:Medicine (General) ,Coronavirus Infections ,030217 neurology & neurosurgery - Abstract
Background In December 2019, pneumonia associated with the 2019 novel coronavirus (COVID-19) emerged in Wuhan, China. The number of cases has increased rapidly. Patients with severe disease have a poor prognosis, and there are no effective therapies for COVID-19. Only rapid advice guidelines for symptomatic supportive care have been used. A traditional Chinese medicine rehabilitation (TCMR) program consisting of acupressure therapy and Liu Zi Jue Qigong can be used as a complementary therapy for COVID-19. Hence, we designed a randomized trial to evaluate the efficacy and advantages of TCMR for treating patients with severe COVID-19. Methods/design This is a parallel-design, two-arm, analyst assessor-blinded, randomized controlled trial. A total of 128 patients with COVID-19 aged from 20 to 80 years will be recruited and assigned randomly into a guideline therapy group and a guideline therapy plus TCMR group at a 1:1 ratio. Patients in both groups will receive guideline therapy. The patients in the intervention group will perform acupressure therapy and Liu Zi Jue Qigong exercises in addition to conventional treatments twice a day and will be persistent from admission to discharge. The primary outcome will be measured with the Modified Medical Research Council Dyspnea Scale, and the secondary outcomes will include the Activities of Daily Living Barthel Index Scale, Patient Health Questionnaire-9 Scale, and the Respiratory Symptoms Scale. The assessments of the clinical scales will be performed at three points (before treatment, the 7th day during hospitalization, and the discharge day). Adverse events will be noted and recorded for the safety evaluation. Discussion This trial will provide high-quality evidence of the value of TCMR, which consists of acupressure therapy and Liu Zi Jue Qigong exercises, for treating patients with severe COVID-19. Trial registration Chinese Clinical Trial Registry ChiCTR2000029994. Registered on 18 February 2020
- Published
- 2020