Engaging children and families in pediatric Health Research: a scoping review

Author:

Flynn RachelORCID,Walton Sarah,Scott Shannon D.

Abstract

Abstract Aim Patient engagement (PE) in pediatric health services research is challenging due to contextual factors such as busyness of parenting, work schedules, and diverse family structures. This scoping review seeks to comprehensively map current PE strategies with parents and families across existing published pediatric health research literature. Methods We followed Arksey and O’Malley (2005) and Levac et al., (2010) six-stage scoping review process. We conducted the search strategy in Medline, Embase, CINAHL, and Psychinfo databases. Data were extracted from included articles; evidence tables were developed and narrative synthesis was completed. Results Of 3925 retrieved records, seventeen articles were included in the review. Patient engagement primarily occurred through strategies such as advisory groups, meetings, focus groups and interviews. Strategies were used to engage patients at various levels, for different purposes (e.g., to inform, participate, consult, involve collaborate and/or lead). These strategies were also used at various stages of the research process. Navigating power differences, time and money were commonly reported challenges. Inconsistent terminology plagued (e.g., stakeholder engagement, consumer participation, patient and public involvement, participatory research) this body of literature and clarity is urgently needed. Conclusions This review offers insights into current PE strategies used in pediatric health services research and offers insight for researchers considering employing PE in the future.

Publisher

Springer Science and Business Media LLC

Subject

General Health Professions,Health (social science)

Reference39 articles.

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3. Domecq JP, Prutsky G. Tarig Elraiyah, et al. patient engagement in research: a systematic review. BMC Health Serv Res. 2014;14(1):1–21. https://doi.org/10.1186/1472-6963-14-89 .

4. Brett J, Staniszewska S, Mockford C, et al. A systematic review of the impact of patient and public involvement on service users, researchers and communities. Patient. 2014;7(4):387–95. https://doi.org/10.1007/s40271-014-0065-0 .

5. Nass P, Levine S, Yancy, C. Methods for involving patients in topic generation for patient-centered comparative effectiveness research, an international perspective- white paper. https://www.pcori.org/assets/Methods-for-Involving-Patients-in-Topic-Generation-for-Patient-Centered-Comparative-Effectiveness-Research-%E2%80%93-An-International-Perspective.pdf . Published March 2012. Accessed Dec 10, 2018.

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