Table 3.
N = 31 trials (%) | |
---|---|
Did sample size/power calculations account for the cluster design? | |
Not presented₳ | 11 (35%) |
Yes, used patient-level data and accounted for clustering (e.g., random effects model) | 11 (35%) |
Yes, used cluster-level summaries | 3 (10%) |
No, used patient-level data without accounting for clustering | 3 (10%) |
Unclear | 1 (3%) |
Other¥ | 2 (6%) |
Did the analysis for primary outcome account for clustering? | |
Yes, used patient-level data and accounted for clustering | 17 (55%) |
Yes, used cluster-level summaries | 5 (16%) |
No, used patient-level data without accounting for clustering ₱ | 7 (23%) |
Unclear/other¥ | 2 (6%) |
Justification for utilizing a cluster randomized design (categories were not mutually exclusive) | |
None provided | 16 (52%) |
Avoid contamination | 15 (48%) |
Logistical or administrative convenience | 2 (6%) |
₳One study presented power calculation, but it was a post hoc power analysis
¥This may have included using an inappropriate method for the proposed primary outcome, or the study accounted for clustering but not based on the primary outcome measure (e.g., they assumed a continuous outcome, but the primary endpoint was a proportion)
₱One study accounted for repeated events within patients but did not report accounting for within-cluster correlation; another study reported using a generalized linear mixed model but did not specify whether they accounted for the effect of the cluster as random effect