| dc.contributor.author | Hooper, R | |
| dc.contributor.author | Copas, A | |
| dc.date.accessioned | 2020-11-30T15:01:58Z | |
| dc.date.available | 2020-09-18 | |
| dc.date.available | 2020-11-30T15:01:58Z | |
| dc.identifier.issn | 1740-7745 | |
| dc.identifier.uri | https://qmro.qmul.ac.uk/xmlui/handle/123456789/68807 | |
| dc.description.abstract | Cluster randomised trials, like individually randomised trials, may benefit from a baseline period of data collection. We consider trials in which clusters prospectively recruit or identify participants as a continuous process over a given calendar period, and ask whether and for how long investigators should collect baseline data as part of the trial, in order to maximise precision. | |
| dc.publisher | SAGE Publications | en_US |
| dc.relation.ispartof | Clinical Trials | |
| dc.rights | This is a pre-copyedited, author-produced version accepted for publication in Clinical Trials following peer review. The version of record is available https://journals.sagepub.com/doi/10.1177/1740774520976564 | |
| dc.title | Optimal design of cluster randomised trials with continuous recruitment and prospective baseline period | en_US |
| dc.type | Article | en_US |
| dc.rights.holder | © 2022 by The Society for Clinical Trials | |
| pubs.notes | Not known | en_US |
| pubs.publication-status | Accepted | en_US |
| dcterms.dateAccepted | 2020-09-18 | |
