Publication details

Knowledge mobilization activities to support decision-making by youth, parents, and adults using a systematic and living map of evidence and recommendations on COVID-19: protocol for three randomized controlled trials and qualitative user-experience studies

Authors

CHARIDE Rana STALLWOOD Lisa MUNAN Matthew SAYFI Shahab HARTLING Lisa BUTCHER Nancy J OFFRINGA Martin ELLIOTT Sarah RICHARDS Dawn P MATHEW Joseph L AKL Elie A KREDO Tamara MBUAGBAW Lawrence MOTILLAL Ashley BABA Ami PREBEG Matthew RELIHAN Jacqueline SCOTT Shannon D SUVADA Jozef FALAVIGNA Maicon KLUGAR Miloslav LOTFI Tamara STEVENS Adrienne POTTIE Kevin SCHUNEMANN Holger J

Year of publication 2023
Type Article in Periodical
Magazine / Source Trials
MU Faculty or unit

Faculty of Medicine

Citation
Web https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-023-07067-9
Doi http://dx.doi.org/10.1186/s13063-023-07067-9
Keywords eCOVID RecMap; COVID-19; Plain language recommendation; Standard language versions; Randomized controlled trial; Knowledge mobilization; Public engagement
Description Introduction The COVID-19 pandemic underlined that guidelines and recommendations must be made more accessible and more understandable to the general public to improve health outcomes. The objective of this study is to evaluate, quantify, and compare the public's understanding, usability, satisfaction, intention to implement, and preference for different ways of presenting COVID-19 health recommendations derived from the COVID-19 Living Map of Recommendations and Gateway to Contextualization (RecMap).Methods and analysis This is a protocol for a multi-method study. Through an online survey, we will conduct pragmatic allocation-concealed, blinded superiority randomized controlled trials (RCTs) in three populations to test alternative formats of presenting health recommendations: adults, parents, and youth, with at least 240 participants in each population. Prior to initiating the RCT, our interventions will have been refined with relevant stakeholder input. The intervention arm will receive a plain language recommendation (PLR) format while the control arm will receive the corresponding original recommendation format as originally published by the guideline organizations (standard language version). Our primary outcome is understanding, and our secondary outcomes are accessibility and usability, satisfaction, intended behavior, and preference for the recommendation formats. Each population's results will be analyzed separately. However, we are planning a meta-analysis of the results across populations. At the end of each survey, participants will be invited to participate in an optional one-on-one, virtual semi-structured interview to explore their user experience. All interviews will be transcribed and analyzed using the principles of thematic analysis and a hybrid inductive and deductive approach.Ethics and dissemination Through Clinical Trials Ontario, the Hamilton Integrated Research Ethics Board has reviewed and approved this protocol (Project ID: 3856). The University of Alberta has approved the parent portion of the trial (Project ID:00114894). Findings from this study will be disseminated through open-access publications in peer-reviewed journals and using social media.

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