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Published in: BMC Medical Research Methodology 1/2013

Open Access 01-12-2013 | Research article

Perspectives on neurological patient registries: a literature review and focus group study

Authors: Lawrence Korngut, Gail MacKean, Lisa Casselman, Megan Johnston, Lundy Day, Darren Lam, Diane Lorenzetti, Janet Warner, Nathalie Jetté, Tamara Pringsheim

Published in: BMC Medical Research Methodology | Issue 1/2013

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Abstract

Background

Patient registries represent a well-established methodology for prospective data collection with a wide array of applications for clinical research and health care administration. An examination and synthesis of registry stakeholder perspectives has not been previously reported in the literature.

Methods

To inform the development of future neurological registries we examined stakeholder perspectives about such registries through a literature review followed by 3 focus groups comprised of a total of 15 neurological patients and 12 caregivers.

Results

(1) Literature review: We identified 6,435 abstracts after duplicates were removed. Of these, 410 articles underwent full text review with 24 deemed relevant to perspectives about neurological and non-neurological registries and were included in the final synthesis. From a patient perspective the literature supports altruism, responsible use of data and advancement of research, among others, as motivating factors for participating in a patient registry. Barriers to participation included concerns about privacy and participant burden (i.e. extra clinic visits and associated costs). (2) Focus groups: The focus groups identified factors that would encourage participation such as: having a clear purpose; low participant burden; and being well-managed among others.

Conclusions

We report the first examination and synthesis of stakeholder perspectives on registries broadly with a specific focus on neurological patient registries. The findings of the broad literature review were congruent with the neurological patient and caregiver focus groups. We report common themes across the literature and the focus groups performed. Stakeholder perspectives need to be considered when designing and operating patient registries. Emphasizing factors that promote participation and mitigating barriers may enhance patient recruitment.
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Metadata
Title
Perspectives on neurological patient registries: a literature review and focus group study
Authors
Lawrence Korngut
Gail MacKean
Lisa Casselman
Megan Johnston
Lundy Day
Darren Lam
Diane Lorenzetti
Janet Warner
Nathalie Jetté
Tamara Pringsheim
Publication date
01-12-2013
Publisher
BioMed Central
Published in
BMC Medical Research Methodology / Issue 1/2013
Electronic ISSN: 1471-2288
DOI
https://doi.org/10.1186/1471-2288-13-135

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