TY - JOUR
T1 - Analysis of recurrent events in cluster randomised trials: The PLEASANT trial case study
AU - Grant, Kelly
AU - Julious, Steven A.
N1 - Data availability statement: Access to patient-level data is provided by the CPRD for health research purposes and is dependent on the approval of a study protocol by the MHRA Independent Expert Advisory Committee (ERC). More information on ERC and the protocol submission process can be found at: https://cprd.com/data-access [accessed 23/11/2022].
Funding: The author(s) received no financial support for the research, authorship, and/or publication of this article.
PY - 2025/6
Y1 - 2025/6
N2 - Recurrent events for many clinical conditions, such as asthma, can indicate poor health outcomes. Recurrent events data are often analysed using statistical methods such as Cox regression or negative binomial regression, suffering event or time information loss. This article re-analyses the preventing and lessening exacerbations of asthma in school-age children associated with a new term (PLEASANT) trial data as a case study, investigating the utility, extending recurrent events survival analysis methods to cluster randomised trials. A conditional frailty model is used, with the frailty term at the general practitioner practice level, accounting for clustering. A rare events bias adjustment is applied if few participants had recurrent events and truncation of small event risk sets is explored, to improve model accuracy. Global and event-specific estimates are presented, alongside a mean cumulative function plot to aid interpretation. The conditional frailty model global results are similar to PLEASANT results, but with greater precision (include time, recurrent events, within-participant dependence, and rare events adjustment). Event-specific results suggest an increasing risk reduction in medical appointments for the intervention group, in September–December 2013, as medical contacts increase over time. The conditional frailty model is recommended when recurrent events are a study outcome for clinical trials, including cluster randomised trials, to help explain changes in event risk over time, assisting clinical interpretation.
AB - Recurrent events for many clinical conditions, such as asthma, can indicate poor health outcomes. Recurrent events data are often analysed using statistical methods such as Cox regression or negative binomial regression, suffering event or time information loss. This article re-analyses the preventing and lessening exacerbations of asthma in school-age children associated with a new term (PLEASANT) trial data as a case study, investigating the utility, extending recurrent events survival analysis methods to cluster randomised trials. A conditional frailty model is used, with the frailty term at the general practitioner practice level, accounting for clustering. A rare events bias adjustment is applied if few participants had recurrent events and truncation of small event risk sets is explored, to improve model accuracy. Global and event-specific estimates are presented, alongside a mean cumulative function plot to aid interpretation. The conditional frailty model global results are similar to PLEASANT results, but with greater precision (include time, recurrent events, within-participant dependence, and rare events adjustment). Event-specific results suggest an increasing risk reduction in medical appointments for the intervention group, in September–December 2013, as medical contacts increase over time. The conditional frailty model is recommended when recurrent events are a study outcome for clinical trials, including cluster randomised trials, to help explain changes in event risk over time, assisting clinical interpretation.
KW - Cluster randomised
KW - conditional frailty
KW - recurrent events
UR - http://www.scopus.com/inward/record.url?scp=105006460731&partnerID=8YFLogxK
U2 - 10.1177/09622802251316972
DO - 10.1177/09622802251316972
M3 - Article
SN - 0962-2802
VL - 34
SP - 1079
EP - 1096
JO - Statistical Methods in Medical Research
JF - Statistical Methods in Medical Research
IS - 6
ER -