Literature DB >> 31258989

Examining the Needs of Patient Stakeholders as Research Partners in Health Data Networks for Translational Research.

Kari A Stephens1,2, Katie P Osterhage3, Brittany Fiore-Gartland4, Terri L Lovins5, Gina A Keppel3, Katherine K Kim6.   

Abstract

Patient stakeholders are getting increasingly involved in research health data networks, particularly as research partners. However, tools do not exist to help effectively orient, educate, and engage patient stakeholders as they take on these roles. Using a human centered design approach, we conducted a patient stakeholder needs assessment qualitative study to identify key user needs to drive design recommendations for development of an online education and engagement tool for research health data networks. We found three key needs related to multiple role identities, motivations and expectations for participation on research teams, and patient journeys. Design recommendations derived from the needs assessment are discussed that can support future tool design and testing.

Entities:  

Year:  2019        PMID: 31258989      PMCID: PMC6568099     

Source DB:  PubMed          Journal:  AMIA Jt Summits Transl Sci Proc


  2 in total

1.  Phenotyping severity of patient-centered outcomes using clinical notes: A prostate cancer use case.

Authors:  Selen Bozkurt; Rohan Paul; Jean Coquet; Ran Sun; Imon Banerjee; James D Brooks; Tina Hernandez-Boussard
Journal:  Learn Health Syst       Date:  2020-07-17

2.  Patient and Patient Group Engagement in Cancer Clinical Trials: A Stakeholder Charter.

Authors:  Stéphanie Michaud; Judy Needham; Stephen Sundquist; Dominique Johnson; Sabrina Hanna; Sharareh Hosseinzadeh; Vatche Bartekian; Patricia Steele; Sarita Benchimol; Nathalie Ross; Barry D Stein
Journal:  Curr Oncol       Date:  2021-04-08       Impact factor: 3.677

  2 in total

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