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. 2022 Mar 9;2022(3):CD015125. doi: 10.1002/14651858.CD015125

Risk of bias for analysis 1.1 All‐cause mortality at up to day 30.

Study Bias
Randomisation process Deviations from intended interventions Missing outcome data Measurement of the outcome Selection of the reported results Overall
Authors' judgement Support for judgement Authors' judgement Support for judgement Authors' judgement Support for judgement Authors' judgement Support for judgement Authors' judgement Support for judgement Authors' judgement Support for judgement
Clemency 2021 Low risk of bias We judged this domain low as the randomisation process was adequate because it is done remotely and moreover consider concealment adequate. Slight baseline differences were most likely due to chance. Low risk of bias Deviations were balanced and most likely not due to the trial context in this double‐blinded trial. Low risk of bias Although there were around 5% of participants lost to follow‐up, it seems not probable that the outcome has been affected relevantly by those dropouts. Low risk of bias We judged low risk of bias, scheduled contact at day 30. Low risk of bias We judged this domain low due to pre‐specification of the outcome. Low risk of bias Overall, we judged low risk of bias.
Ramakrishnan 2021 Low risk of bias Stratified block randomisation, sequence held in secure network location at Oxford University, characteristics incl. SARS‐CoV‐2 status are well balanced. Low risk of bias We judged this domain low due to only a low number of participants withdrew consent. Low risk of bias We judged this domain low due to a small number of missing data. In the intervention group about 1% and in the control group about 4% of the participants withdrew consent due to the allocation. Low risk of bias We judged this domain low because the measurements were similar between groups. Some concerns We judged some concerns because the outcome was not pre‐specified. Some concerns Overall we judged some concerns due to missing pre‐specification of the outcome.
Yu 2021 Low risk of bias Participants were randomised via web‐based Sortition and the allocation sequence was intimated to GP and patient via email/letter. There are no baseline differences that would suggest a problem with randomisation Low risk of bias We judged risk of bias low because there were no reported deviations from intended interventions. Low risk of bias We judged this domain low because it is not likely that missingness in the outcome depended on its true value. There were about 5% of the participants without a diary entry. Low risk of bias We judged this domain low because the measurements were similar between groups. Low risk of bias The data were in accordance with the protocol, so that we assessed this domain low. Low risk of bias Overall judged low risk of bias.