The partnership of patient advocacy groups and clinical investigators in the rare diseases clinical research network. Issue 1 (December 2016)
- Record Type:
- Journal Article
- Title:
- The partnership of patient advocacy groups and clinical investigators in the rare diseases clinical research network. Issue 1 (December 2016)
- Main Title:
- The partnership of patient advocacy groups and clinical investigators in the rare diseases clinical research network
- Authors:
- Merkel, Peter
Manion, Michele
Gopal-Srivastava, Rashmi
Groft, Stephen
Jinnah, H.
Robertson, David
Krischer, Jeffrey - Abstract:
- Abstract Background Among the unique features of the Rare Diseases Clinical Research Network (RDCRN) Program is the requirement for each Consortium to include patient advocacy groups (PAGs) as research partners. This development has transformed the work of the RDCRN and is a model for collaborative research. This article outlines the roles patients and PAGs play in the RDCRN and reports on the PAGs' impact on the Network's success. Methods Principal Investigators from the 17 RDCRN Consortia and 28 representatives from 76 PAGs affiliated with these Consortia were contacted by email to provide feedback via an online RDCRN survey. Impact was measured in the key areas of 1) Research logistics; 2) Outreach and communication; and 3) Funding and in-kind support. Rating choices were: 1-very negative, 2-somewhat negative, 3-no impact, 4-somewhat positive, and 5-very positive. Results Twenty-seven of the PAGs (96 %) disseminate information about the RDCRN within the patient community. The Consortium Principal Investigators also reported high levels of PAG involvement. Sixteen (94 %) Consortium Principal Investigators and 25 PAGs (89 %) reported PAGs participation in protocol review, study design, Consortium conference calls, attending Consortium meetings, or helping with patient recruitment. Conclusions PAGs are actively involved in shaping Consortia's research agendas, help ensure the feasibility and success of research protocols by assisting with study design and patientAbstract Background Among the unique features of the Rare Diseases Clinical Research Network (RDCRN) Program is the requirement for each Consortium to include patient advocacy groups (PAGs) as research partners. This development has transformed the work of the RDCRN and is a model for collaborative research. This article outlines the roles patients and PAGs play in the RDCRN and reports on the PAGs' impact on the Network's success. Methods Principal Investigators from the 17 RDCRN Consortia and 28 representatives from 76 PAGs affiliated with these Consortia were contacted by email to provide feedback via an online RDCRN survey. Impact was measured in the key areas of 1) Research logistics; 2) Outreach and communication; and 3) Funding and in-kind support. Rating choices were: 1-very negative, 2-somewhat negative, 3-no impact, 4-somewhat positive, and 5-very positive. Results Twenty-seven of the PAGs (96 %) disseminate information about the RDCRN within the patient community. The Consortium Principal Investigators also reported high levels of PAG involvement. Sixteen (94 %) Consortium Principal Investigators and 25 PAGs (89 %) reported PAGs participation in protocol review, study design, Consortium conference calls, attending Consortium meetings, or helping with patient recruitment. Conclusions PAGs are actively involved in shaping Consortia's research agendas, help ensure the feasibility and success of research protocols by assisting with study design and patient recruitment, and support training programs. This extensive PAG-Investigator partnership in the RDCRN has had a strongly positive impact on the success of the Network. … (more)
- Is Part Of:
- Orphanet journal of rare diseases. Volume 11:Issue 1(2016)
- Journal:
- Orphanet journal of rare diseases
- Issue:
- Volume 11:Issue 1(2016)
- Issue Display:
- Volume 11, Issue 1 (2016)
- Year:
- 2016
- Volume:
- 11
- Issue:
- 1
- Issue Sort Value:
- 2016-0011-0001-0000
- Page Start:
- 1
- Page End:
- 10
- Publication Date:
- 2016-12
- Subjects:
- Rare diseases -- Patient engagement -- Network
Rare diseases -- Periodicals
Genetic disorders -- Periodicals
Orphan drugs -- Periodicals
616 - Journal URLs:
- http://pubmedcentral.com/tocrender.fcgi?journal=401&action=archive ↗
http://www.ojrd.com/home/ ↗
http://link.springer.com/ ↗ - DOI:
- 10.1186/s13023-016-0445-8 ↗
- Languages:
- English
- ISSNs:
- 1750-1172
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 9889.xml