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Randomized Controlled Trial
. 2022 May 26;17(1):34.
doi: 10.1186/s13012-022-01208-5.

A randomised fractional factorial screening experiment to predict effective features of audit and feedback

Affiliations
Randomized Controlled Trial

A randomised fractional factorial screening experiment to predict effective features of audit and feedback

Alexandra Wright-Hughes et al. Implement Sci. .

Abstract

Background: Audit and feedback aims to improve patient care by comparing healthcare performance against explicit standards. It is used to monitor and improve patient care, including through National Clinical Audit (NCA) programmes in the UK. Variability in effectiveness of audit and feedback is attributed to intervention design; separate randomised trials to address multiple questions about how to optimise effectiveness would be inefficient. We evaluated different feedback modifications to identify leading candidates for further "real-world" evaluation.

Methods: Using an online fractional factorial screening experiment, we randomised recipients of feedback from five UK NCAs to different combinations of six feedback modifications applied within an audit report excerpt: use effective comparators, provide multimodal feedback, recommend specific actions, provide optional detail, incorporate the patient voice, and minimise cognitive load. Outcomes, assessed immediately after exposure to the online modifications, included intention to enact audit standards (primary outcome, ranked on a scale of -3 to +3, tailored to the NCA), comprehension, user experience, and engagement.

Results: We randomised 1241 participants (clinicians, managers, and audit staff) between April and October 2019. Inappropriate repeated participant completion occurred; we conservatively excluded participant entries during the relevant period, leaving a primary analysis population of 638 (51.4%) participants. None of the six feedback modifications had an independent effect on intention across the five NCAs. We observed both synergistic and antagonistic effects across outcomes when modifications were combined; the specific NCA and whether recipients had a clinical role had dominant influences on outcome, and there was an antagonistic interaction between multimodal feedback and optional detail. Among clinical participants, predicted intention ranged from 1.22 (95% confidence interval 0.72, 1.72) for the least effective combination in which multimodal feedback, optional detail, and reduced cognitive load were applied within the audit report, up to 2.40 (95% CI 1.88, 2.93) for the most effective combination including multimodal feedback, specific actions, patient voice, and reduced cognitive load.

Conclusion: Potentially important synergistic and antagonistic effects were identified across combinations of feedback modifications, audit programmes, and recipients, suggesting that feedback designers must explicitly consider how different features of feedback may interact to achieve (or undermine) the desired effects.

Trial registration: International Standard Randomised Controlled Trial Number: ISRCTN41584028.

Keywords: Audit and feedback; Behaviour change; MOST; Randomised fractional factorial experiment.

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Conflict of interest statement

Thomas Willis, Sarah Alderson, Fabiana Lorencatto, Jillian Francis, Jamie Brehaut, Heather Colquhoun, Noah Ivers, Benjamin Brown, Rebecca Walwyn, and Robbie Foy are members of the Audit and Feedback MetaLab. The MetaLab is an international collaboration to advance learning and expertise on audit and feedback and promotes the development of A&F implementation laboratories internationally. Justin Presseau is an Associate Editor of Implementation Science, and Robbie Foy, Noah Ivers, and Fabiana Lorencatto are editorial board members.

Figures

Fig. 1
Fig. 1
Experiment summary — participant flow
Fig. 2
Fig. 2
Distribution of the primary outcome by NCA and role
Fig. 3
Fig. 3
Distribution of secondary outcomes
Fig. 4
Fig. 4
Primary outcome: Pareto plot of standardised effects (primary outcome, stage-2 full model)
Fig. 5
Fig. 5
Predicted intention for modification combinations ordered by clinical recipients (results/estimates presented for the NDA only; however, relative effectiveness of modification combinations is consistent across NCAs)

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