Trial N/A
Publication Liu K, Complement Ther Clin Pract, 2020
Funding: * ()
Methods | |
RCT | |
Location :
Multicenter / China Follow-up duration (days): 42 | |
Inclusion criteria | (1) with a definite diagnosis of COVID-19; (2)aged 65 years or above; (3) at least 6 months after the onset of other acutediseases; (4) mini-mental state examination (MMSE) score > 21; (6) noCOPD or any other respiratory disease; and (7) forced expiratory volumein 1 s (FEV1) at least 70%. |
Exclusion criteria | (1) moderate or severe heartdisease (Grade III or IV, New York Heart Association); (2) with severeischemic or hemorrhagic stroke or neurodegenerative diseases. |
Interventions | |
Treatment
Respiratory rehabilitation (Once a day for 10 minutes (home ) Duration : 6 weeks |
|
Control
No respiratory rehabilitation | |
Participants | |
Randomized 76 participants (n1=38 / n2= 38) | |
Characteristics of participants N=76 Mean age : 69,2 49 males | |
Primary outcome | |
In the register NR | |
In the report | |
Documents available |
Protocol NR Statistical plan NR Data-sharing stated NR |
Risk of bias Overall The overall risk of bias reported in the table corresponds to the highest risk of bias for the outcomes assessed for the systematic review |
High |
General comment | The study registry, protocol and statistical analysis plan were not available. Whether randomization occured or not, and other information relevant to randomization (i.e., whether random allocation was concealed), is unclear. |