Cargando…
Clinical research associates experience with missing patient reported outcomes data in cancer randomized controlled trials
BACKGROUND: Missing patient reported outcomes data threaten the validity of PRO‐specific findings and conclusions from randomized controlled trials by introducing bias due to data missing not at random. Clinical Research Associates are a largely unexplored source for informing understanding of poten...
Autores principales: | Palmer, Michael J., Krupa, Terry, Richardson, Harriet, Brundage, Michael D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8085912/ https://www.ncbi.nlm.nih.gov/pubmed/33835717 http://dx.doi.org/10.1002/cam4.3826 |
Ejemplares similares
-
International perspectives on suboptimal patient‐reported outcome trial design and reporting in cancer clinical trials: A qualitative study
por: Retzer, Ameeta, et al.
Publicado: (2021) -
Harnessing the patient voice in prostate cancer research: Systematic review on the use of patient‐reported outcomes in randomized controlled trials to support clinical decision‐making
por: Van Hemelrijck, Mieke, et al.
Publicado: (2020) -
Design, implementation and reporting strategies to reduce the instance and impact of missing patient-reported outcome (PRO) data: a systematic review
por: Mercieca-Bebber, Rebecca, et al.
Publicado: (2016) -
Investigating the impact of open label design on patient‐reported outcome results in prostate cancer randomized controlled trials
por: Mouillet, Guillaume, et al.
Publicado: (2020) -
Quality of life outcomes from a randomized controlled trial of patient navigation in Latina breast cancer survivors
por: Ramirez, Amelie G., et al.
Publicado: (2020)