Abstract

BackgroundExploring factors associated with retention in randomised trials provides insight into potential threats to internal and external study validity, and may inform the development of interventions to increase retention in future trials. Given a paucity of existing research in the field, a study was conducted to explore factors associated with retention in a smoking intervention trial involving persons with a mental illness, considering demographic and smoking characteristics, treatment condition and engagement in prior follow-up assessments.MethodA descriptive study was undertaken using data derived from a RCT of a smoking cessation intervention initiated in four adult psychiatric inpatient units in New South Wales (NSW), Australia. Retention assessment was undertaken at 1, 6 and 12-months post-discharge. A Generalised Linear Mixed Model was adopted to explore associations between retention at any follow up time point and demographic and smoking characteristics. Chi square analyses explored the association between retention at all follow up time points and treatment condition, and binary logistic regression analyses assessed for relationships between retention at 12-month follow up and engagement in prior follow up assessments.ResultsRetention rates were 63, 56 and 60% at the 1, 6 and 12-month assessments, respectively. No association was found between retention at any follow-up time point and 13 of 15 demographic and smoking characteristics. Younger participants and those who identified to be Aboriginal and/or Torres Strait Islander were more likely to be retained (both ps > 0.05). Retention rates did not vary according to treatment condition at any follow-up time point. Participants who completed a prior assessment were more likely to complete the 12 month assessment (both prior assessments: OR 10.7, p < 0.001; 6 month assessment: OR 6.01, p < 0.001; and 1 month assessment: OR 1.8, p = 0.002).ConclusionThe underrepresentation of younger participants and those identifying to be Aboriginal and/or Torres Strait Islander may limit the generalisability of findings. Findings suggest that inclusion of multiple contacts during a trial follow up period may increase retention at the final assessment. Interventions to improve retention, overall and for those sub-groups less likely to be retained, in smoking trials involving persons with a mental illness are needed. Further assessment of sample characteristics, and also trial design factors, associated with retention in this field is warranted.

Highlights

  • Exploring factors associated with retention in randomised trials provides insight into potential threats to internal and external study validity, and may inform the development of interventions to increase retention in future trials

  • Design and setting A descriptive study was undertaken using data derived from a two-arm, parallel group randomised controlled trial (RCT) of a smoking cessation intervention initiated in four adult psychiatric inpatient units in New South Wales (NSW), Australia and continued for 4 months post-discharge

  • Sample Three thousand six hundred and twenty-six patients were admitted to the psychiatric inpatient facilities during the recruitment period; 2078 were assessed for eligibility, and 61% (N = 754) of eligible smokers were recruited into the smoking cessation intervention trial (Fig. 1)

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Summary

Introduction

Exploring factors associated with retention in randomised trials provides insight into potential threats to internal and external study validity, and may inform the development of interventions to increase retention in future trials. Given a paucity of existing research in the field, a study was conducted to explore factors associated with retention in a smoking intervention trial involving persons with a mental illness, considering demographic and smoking characteristics, treatment condition and engagement in prior follow-up assessments. Low rates of participant retention at trial end-points or differential retention rates between treatment conditions can compromise the internal (inference that the intervention alone caused changes to outcome, through minimisation of potential confounding variables) and external (generalisability) validity and reduce the statistical power of controlled trials [14, 15]. Given the risk of bias in trial results due to inadequate or differential participant retention, the development of novel approaches to increase retention rates has been identified as a priority for trial methods research [17]

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