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HELP! Problems in executing a pragmatic, randomized, stepped wedge trial on the Hospital Elder Life Program to prevent delirium in older patients

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HELP! Problems in executing a pragmatic, randomized, stepped wedge trial on the Hospital Elder Life Program to prevent delirium in older patients

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Samenvatting

Background: A pragmatic, stepped wedge trial design can be an appealing design to evaluate complex interventions
in real-life settings. However, there are certain pitfalls that need to be considered. This paper reports on the experiences
and lessons learned from the conduct of a cluster randomized, stepped wedge trial evaluating the effect of the Hospital
Elder Life Program (HELP) in a Dutch hospital setting to prevent older patients from developing delirium.
Methods: We evaluated our trial which was conducted in eight departments in two hospitals in hospitalized patients
aged 70 years or older who were at risk for delirium by reflecting on the assumptions that we had and on what we
intended to accomplish when we started, as compared to what we actually realized in the different phases of our study.
Lessons learned on the design, the timeline, the enrollment of eligible patients and the use of routinely collected data
are provided accompanied by recommendations to address challenges.
Results: The start of the trial was delayed which caused subsequent time schedule problems. The requirement for
individual informed consent for a quality improvement project made the inclusion more prone to selection bias. Most
units experienced major difficulties in including patients, leading to excluding two of the eight units from participation.
This resulted in failing to include a similar number of patients in the control condition versus the intervention condition.
Data on outcomes routinely collected in the electronic patient records were not accessible during the study, and
appeared to be often missing during analyses.
Conclusions: The stepped wedge, cluster randomized trial poses specific risks in the design and execution of research in
real-life settings of which researchers should be aware to prevent negative consequences impacting the validity of their
results. Valid conclusions on the effectiveness of the HELP in the Dutch hospital setting are hampered by the limited
quantity and quality of routine clinical data in our pragmatic trial. Executing a stepped wedge design in a daily practice
setting using routinely collected data requires specific attention to ethical review, flexibility, a spacious time schedule, the
availability of substantial capacity in the research team and early checks on the data availability and quality.

Toon meer
OrganisatieHogeschool Utrecht
AfdelingKenniscentrum Gezond en Duurzaam Leven
LectoraatChronisch Zieken
Gepubliceerd inTrials BioMed Central, Uitgave: 18, Pagina: 220
Jaar2017
TypeArtikel
TaalEngels

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