Including the patient voice in the development and implementation of patient‐reported outcomes in cancer clinical trials
Abstract Context Patient‐reported outcomes (PROs) are used in parallel with clinical evidence to inform decisions made by industry, clinicians, regulators, health technology assessment bodies and other health‐care decision‐makers. In addition, PRO data can also guide shared decision making and indiv...
Main Authors: | Bonnie Addario, Jan Geissler, Marcia K. Horn, Linda U. Krebs, Deborah Maskens, Kathy Oliver, Ananda Plate, Erin Schwartz, Nicole Willmarth |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2020-02-01
|
Series: | Health Expectations |
Subjects: | |
Online Access: | https://doi.org/10.1111/hex.12997 |
Similar Items
-
The view of patients and patients’ companions regarding patients’ rights: a phenomenological research
by: Jolaee S, et al.
Published: (2004-05-01) -
The view of patients and patients’ companions regarding patients’ rights: a phenomenological research
by: S Jolaee, et al.
Published: (2005-02-01) -
Being a Patient Representative Is More Work Than Being a Patient Advocate—Done Right, It Is Also Likely to Be More Effective
by: Richard Wassersug
Published: (2021-02-01) -
The Importance of Shared Decision-Making for Patients with Glioblastoma
by: Musella A, et al.
Published: (2021-09-01) -
Utilizing patient advocates in Parkinson’s disease: A proposed framework for patient engagement and the modern metrics that can determine its success
by: Megan Feeney, et al.
Published: (2020-08-01)