Cargando…
Patient Governance in a Patient-Powered Research Network for Adult Rheumatologic Conditions
BACKGROUND: Patient-Powered Research Networks (PPRNs) are a unique type of patient-powered patient registry for patient-centered outcomes research requiring that stakeholder engagement play a key role in governance (eg, research guidance and decision making). The purpose of this report is to describ...
Autores principales: | Nowell, W. Benjamin, Curtis, Jeffrey R., Crow-Hercher, Rachelle |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6143204/ https://www.ncbi.nlm.nih.gov/pubmed/30074946 http://dx.doi.org/10.1097/MLR.0000000000000814 |
Ejemplares similares
-
Which patient-reported outcomes do rheumatology patients find important to track digitally? A real-world longitudinal study in ArthritisPower
por: Nowell, W. Benjamin, et al.
Publicado: (2021) -
Tough Choices: Exploring Medication Decision‐Making During Pregnancy and Lactation Among Women With Inflammatory Arthritis
por: Birru Talabi, Mehret, et al.
Publicado: (2021) -
Patient-Powered Research Networks of the Autoimmune Research Collaborative: Rationale, Capacity, and Future Directions
por: Nowell, W. Benjamin, et al.
Publicado: (2021) -
Pregnancy, Periods, and “The Pill”: Exploring the Reproductive Experiences of Women with Inflammatory Arthritis
por: Birru Talabi, Mehret, et al.
Publicado: (2019) -
Harnessing health plan enrollee data to boost membership in patient-powered research networks
por: Chen, Xiaoxue, et al.
Publicado: (2020)