Utilizing patient advocates in Parkinson's disease: A proposed framework for patient engagement and the modern metrics that can determine its success. (3rd May 2020)
- Record Type:
- Journal Article
- Title:
- Utilizing patient advocates in Parkinson's disease: A proposed framework for patient engagement and the modern metrics that can determine its success. (3rd May 2020)
- Main Title:
- Utilizing patient advocates in Parkinson's disease: A proposed framework for patient engagement and the modern metrics that can determine its success
- Authors:
- Feeney, Megan
Evers, Christiana
Agpalo, Danielle
Cone, Lisa
Fleisher, Jori
Schroeder, Karlin - Abstract:
- Abstract: The wide application of patient engagement and its associated benefits has increased across government, academic and pharmaceutical research. However, neither an identified standard practice for the process of engagement, nor utilization of common metrics to assess associated outcomes, exists. Parkinson's Foundation developed a patient engagement framework and metrics to assess engagement within the academic research and drug development sectors. This approach was developed over the course of several years through assessing the literature, acquiring feedback from researchers and people with Parkinson's disease and adapting practices to be relevant and generalizable across patient engagement projects. This framework includes the: 1) creation of a scope of work, 2) establishment of guiding principles, 3) selection and training of participants, 4) co‐determination of project metrics, 5) execution of the project and 6) dissemination of project findings. Parkinson's Foundation has also worked with academic, government and pharmaceutical stakeholders to identify metrics that assess both the quality of patient engagement and outcomes associated with patient engagement on projects. By improving patient engagement project methodologies and metrics, global clinical trials can have access to evidence‐based patient engagement practices to more efficiently capture the needs of, and potentially benefit, the patient community.
- Is Part Of:
- Health expectations. Volume 23:Number 4(2020)
- Journal:
- Health expectations
- Issue:
- Volume 23:Number 4(2020)
- Issue Display:
- Volume 23, Issue 4 (2020)
- Year:
- 2020
- Volume:
- 23
- Issue:
- 4
- Issue Sort Value:
- 2020-0023-0004-0000
- Page Start:
- 722
- Page End:
- 730
- Publication Date:
- 2020-05-03
- Subjects:
- methodology -- metrics -- patient advocacy -- patient empowerment -- patient engagement -- patient involvement
Medical policy -- Periodicals
Public health -- Periodicals
Health planning -- Periodicals
362.105 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=hex ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1369-7625 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/hex.13064 ↗
- Languages:
- English
- ISSNs:
- 1369-6513
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4275.015545
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 14261.xml