Comparing three approaches for involving patients in research prioritization: a qualitative study of participant experiences
Abstract Background By participating in priority-setting activities in research, patients and members of the public help ensure that important questions are incorporated into future research agendas. Surveys, focus groups, and online crowdsourcing are increasingly used to obtain input, yet little is...
Main Authors: | Danielle C. Lavallee, Sarah O. Lawrence, Andrew L. Avins, David R. Nerenz, Todd C. Edwards, Donald L. Patrick, Zoya Bauer, Anjali R. Truitt, Sarah E. Monsell, Mary R. Scott, Jeffrey G. Jarvik |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2020-05-01
|
Series: | Research Involvement and Engagement |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s40900-020-00196-4 |
Similar Items
-
Patient engagement in type 2 diabetes mellitus research: what patients want
by: Simacek KF, et al.
Published: (2018-04-01) -
Patient knowledge, experiences and preferences regarding retinoblastoma and research: A qualitative study
by: Catherine Moses, et al.
Published: (2020-06-01) -
Using concept mapping to prioritize barriers to diabetes care and self-management for those who experience homelessness
by: Eshleen K. Grewal, et al.
Published: (2021-07-01) -
What happens after James Lind Alliance Priority Setting Partnerships? A qualitative study of contexts, processes and impacts
by: Kristina Staley, et al.
Published: (2020-07-01) -
Female genital mutilation in the UK- where are we, where do we go next? Involving communities in setting the research agenda
by: S. Dixon, et al.
Published: (2018-09-01)