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Participant retention in paediatric randomised controlled trials published in six major journals 2015-2019:
Daisy M Gaunt1, Cat Papastavrou Brooks2, Hugo Pedder2
1Population Health Sciences, Bristol Medical School, University of Bristol, Canynge Hall, 39 Whatley Road, Bristol, BS8 2PS, UK. daisy.gaunt@bristol.ac.uk.
Insights
Participant retention in paediatric randomized controlled trials (RCTs) is crucial. Factors like frequent follow-ups, shorter trial durations, and engagement methods significantly improve retention in pediatric research.
Area of Science:
- Clinical Trials
- Pediatric Research
- Health Services Research
Background:
- Participant retention in pediatric randomized controlled trials (RCTs) is under-researched.
- Challenges include child development, multiple participants, and proxy reporting.
- This review explores factors influencing retention in pediatric trials.
Approach:
- Systematic review and meta-analysis of pediatric RCTs published 2015-2019.
- Data extracted on context and design factors influencing retention.
- Univariate random-effects meta-regression analysis used to determine associations.
Key Points:
- Higher retention observed with ≥5 follow-ups, <6 months between randomization and outcome, and inactive data collection.
- Trials with older children (≥11 years) and without additional participants showed better retention.
- Active/placebo controls and engagement methods positively impacted retention.
Conclusions:
- Paediatric RCTs rarely report modifiable factors that enhance retention.
- Multiple, regular pre-outcome follow-ups and outcomes within 6 months may reduce attrition.
- Qualitative research and engagement strategies are recommended for improving retention in pediatric trials.
Background:
The factors which influence participant retention in paediatric randomised controlled trials are under-researched. Retention may be more challenging due to child developmental stages, involving additional participants, and proxy-reporting of outcomes. This systematic review and meta-analysis explores the factors which may influence retention in paediatric trials.
Methods:
Using the MEDLINE database, paediatric randomised controlled trials published between 2015 and 2019 were identified from six general and specialist high-impact factor medical journals. The review outcome was participant retention for each reviewed trial's primary outcome. Context (e.g. population, disease) and design (e.g. length of trial) factors were extracted. Retention was examined for each context and design factor in turn, with evidence for an association being determined by a univariate random-effects meta-regression analysis.
Results:
Ninety-four trials were included, and the median total retention was 0.92 (inter-quartile range 0.83 to 0.98). Higher estimates of retention were seen for trials with five or more follow-up assessments before the primary outcome, those less than 6 months between randomisation and primary outcome, and those that used an inactive data collection method. Trials involving children aged 11 and over had the higher estimated retention compared with those involving younger children. Those trials which did not involve other participants also had higher retention, than those where they were involved. There was also evidence that a trial which used an active or placebo control treatment had higher estimated retention, than treatment-as-usual. Retention increased if at least one engagement method was used. Unlike reviews of trials including all ages of participants, we did not find any association between retention and the number of treatment groups, size of trial, or type of treatment.
Conclusions:
Published paediatric RCTs rarely report the use of specific modifiable factors that improve retention. Including multiple, regular follow-ups with participants before the primary outcome may reduce attrition. Retention may be highest when the primary outcome is collected up to 6 months after a participant is recruited. Our findings suggest that qualitative research into improving retention when trials involve multiple participants such as young people, and their caregivers or teachers would be worthwhile. Those designing paediatric trials also need to consider the use of appropriate engagement methods. RESEARCH ON RESEARCH (ROR) REGISTRY: https://ror-hub.org/study/2561.
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