Development and evaluation of a parent advisory group to inform a research program for knowledge translation in child health

Author:

Hartling LisaORCID,Elliott Sarah A.,Buckreus Kelli,Leung Julie,Scott Shannon D.

Abstract

Abstract Background In response to a growing movement to involve patients and community stakeholders in health research, we established a parent advisory group in 2016. The group meets regularly to act as advisors and partners for our research program. The purpose of this paper is to describe our experiences establishing the group, and results from parent evaluations. Methods We contacted 191 organizations to recruit parents and caregivers of children who wanted to contribute to child health research. Our initial goal was to recruit 8 to 10 parents who would meet regularly (approximately 8 times per year). We conducted an online baseline survey of members after the first two meetings to understand motivations for participating and early experiences. Sixteen months later we conducted another online survey to identify what was going well and areas for improvement. Results Twelve parents initially joined the group. The baseline survey (n = 9 complete) identified motivations for participation: wanting a patient/family voice in health research; personal experience accessing health system for child’s care; wanting to improve healthcare communications. Concerns about participation included: having sufficient time to attend meetings; whether contributions would be worthwhile; and uncertainty about how the group’s input would be used in practice. Parents identified aspects that were working well: opportunity to provide constructive feedback; diversity among parents involved; well-run and organized meetings (agenda and materials sent prior to meeting, skilled facilitation, adequate time for discussion). Items parents identified as not working well were: fluctuating attendance; not knowing others in the group; challenges if attending remotely. At follow-up, there were seven active members. The follow-up survey (n = 5 complete) identified positive feedback related to group dynamics (e.g., collegial, everyone participates) and organization of meetings. Suggestions for improvement included increasing membership, regular attendance, and providing adequate information/context to allow meaningful input. Conclusions Our experience establishing a parent advisory group and evaluation of the group by parent members have yielded tremendous insights around involving parents and patient proxies in health research. The parent advisory group is a dynamic entity requiring ongoing communication between researchers and members. Effective means of evaluating engagement is essential to ensure it is meaningful. Dedicated time, funding and resources are required for success.

Funder

Stollery Children’s Hospital Foundation

Alberta Innovates - Health Solutions

Publisher

Springer Science and Business Media LLC

Subject

General Health Professions,Health(social science)

Reference20 articles.

1. Canadian Institutes of Health Research. Canada’s Strategy for Patient-Oriented Research: Improving health outcomes through evidence-informed care. https://cihr-irsc.gc.ca/e/44000.html, Accessed 8 Sept 2020.

2. National Center for Research Resources. Strategic plan 2009-2013. NIH Publication No. 08–6439. Bethesda: National Center for Research Resources, National Institutes of Health; 2008.

3. United Kingdom Clinical Research Collaboration. UK Clinical Research Collaboration progress report, 2006-2008. United Kingdom: UKCRC (United Kingdom Clinical Research Collaboration); 2008.

4. Department of Innovation, Industry, Science and Research, Australian Government. Strategic roadmap for Australian research infrastructure. 2008.

5. National Health and Medical Research Council. Clinical research in Australia. Report of the NHMRC Clinical Research Working Group. Australia: NHMRC (National Health and Medical Research Council); 2001.

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