Cargando…
The importance of patient-reported outcomes in clinical trials and strategies for future optimization
Patient-reported outcomes (PROs) can be included in clinical trials as primary or secondary endpoints and are increasingly recognized by regulators, clinicians, and patients as valuable tools to collect patient-centered data. PROs provide unique information on the impact of a medical condition and i...
Autores principales: | Mercieca-Bebber, Rebecca, King, Madeleine T, Calvert, Melanie J, Stockler, Martin R, Friedlander, Michael |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219423/ https://www.ncbi.nlm.nih.gov/pubmed/30464666 http://dx.doi.org/10.2147/PROM.S156279 |
Ejemplares similares
-
A systematic evaluation of compliance and reporting of patient-reported outcome endpoints in ovarian cancer randomised controlled trials: implications for generalisability and clinical practice
por: Mercieca-Bebber, Rebecca, et al.
Publicado: (2017) -
The administration of patient-reported outcome questionnaires in cancer trials: Interviews with trial coordinators regarding their roles, experiences, challenges and training
por: Mercieca-Bebber, Rebecca, et al.
Publicado: (2017) -
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) -
A practical guide to understanding, using and including patient reported outcomes in clinical trials in ovarian cancer
por: Wilson, Michelle K., et al.
Publicado: (2018) -
Patient-Reported Outcome (PRO) Assessment in Clinical Trials: A Systematic Review of Guidance for Trial Protocol Writers
por: Calvert, Melanie, et al.
Publicado: (2014)