Identifying the knowledge needs and preferences of parents of children with rare diseases regarding clinical trials: a scoping review protocol

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Publication Details

Journal
Systematic Reviews
Published
2026-02-05
DOI
https://doi.org/10.1186/s13643-026-03094-0
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
0.00

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article

Identifying the knowledge needs and preferences of parents of children with rare diseases regarding clinical trials: a scoping review protocol

Annie P. Mabbott, Lisa Knisley, Shannon D. Scott
Systematic Reviews
Genomics and Rare Diseases
article

Identifying the knowledge needs and preferences of parents of children with rare diseases regarding clinical trials: a scoping review protocol

Annie P. Mabbott, Lisa Knisley, Shannon D. Scott
article en

Abstract

No abstract available for this paper.
Systematic ReviewsVol. 15(1)
University of Alberta (CA), Stollery Children's Hospital (CA), University of Manitoba (CA)
University of Alberta, Canadian Institutes of Health Research
Quality Education
Openalex Percentile: Top 63%
Genomics and Rare Diseases
DOIOpen Access PDFOpenAlex
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