Evidence map›Paper›PMID 35619097›Full record

Trial reportImplementation science : IS2022

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

Alexandra Wright-Hughes, Thomas A Willis, Stephanie Wilson, Ana Weller, Fabiana Lorencatto, Mohamed Althaf, Valentine Seymour, Amanda J Farrin, Jillian Francis, Jamie Brehaut and 11 more

Abstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Implementation science : IS, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Alexandra Wright-HughesLeeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK. a.wright-hughes@leeds.ac.uk.ORCID 0000-0001-8839-6756
Thomas A WillisLeeds Institute of Health Sciences, University of Leeds, Leeds, UK.
Stephanie WilsonCentre for Human-Computer Interaction Design, City, University of London, London, UK.
Ana WellerCentre for Human-Computer Interaction Design, City, University of London, London, UK.
Fabiana LorencattoCentre for Behaviour Change, University College London, London, UK.
Mohamed AlthafCentre for Human-Computer Interaction Design, City, University of London, London, UK.
Valentine SeymourCentre for Human-Computer Interaction Design, City, University of London, London, UK.
Amanda J FarrinLeeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK.
Jillian FrancisSchool of Health Sciences, University of Melbourne, Melbourne, Australia.
Jamie BrehautOttawa Hospital Research Institute, Ottawa, Canada.
Noah IversDepartment of Family and Community Medicine, Womens College Hospital, University of Toronto, Toronto, Canada.
Sarah L AldersonLeeds Institute of Health Sciences, University of Leeds, Leeds, UK.
Benjamin C BrownCentre for Health Informatics, University of Manchester, Manchester, UK.
Richard G FeltbowerLeeds Institute for Data Analytics, School of Medicine, University of Leeds, Leeds, UK.
Chris P GaleLeeds Institute for Data Analytics, School of Medicine, University of Leeds, Leeds, UK.
Simon J StanworthTransfusion Medicine, NHS Blood and Transplant (NHSBT), Oxford, UK.
Suzanne HartleyLeeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK.
Heather ColquhounDepartment of Occupational Science and Occupational Therapy, University of Toronto, Toronto, Canada.
Justin PresseauOttawa Hospital Research Institute, Ottawa, Canada.
Rebecca Walwyn *Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK.
Robbie Foy *Leeds Institute of Health Sciences, University of Leeds, Leeds, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAudit 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.

methodsUsing 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.

resultsWe 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.

conclusionPotentially 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 registrationInternational Standard Randomised Controlled Trial Number: ISRCTN41584028.

Indexed as

Clinical AuditMedical AuditFeedbackHealth Services ResearchHumansIntentionAudit and feedbackBehaviour changeMOSTRandomised fractional factorial experiment

Identifiers

PMID35619097
PMCPMC9137082

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.