Patient Voices Project

The role patients, caregivers, and family members play in healthcare and healthcare research is rapidly evolving. The traditional paradigm, placing patients as passive recipients of care and information, is shifting to one where patients are seen as partners and collaborators not only in the care they receive but in how evidence is generated. The CERTAIN Patient Voices Project supports collaboration between patient, research, and clinician communities to improve the quality of healthcare delivery and research.

The Patient Voices Project has three primary goals:

  • To develop and sustain meaningful and interactive collaborations with the Patient Advisory Network to help inform the research process – from the questions asked to the dissemination of research findings;
  • To develop and sustain a patient- reported outcomes (PROs) registry that complements clinical data used as part of the Washington State Surgical Care and Outcomes Assessment Program (SCOAP) quality improvement initiatives; 
  • To facilitate real-time use of PROs in practice to assist patient and clinician communication and decision-making at the point-of-care, in addition to developing benchmarking data for public access and use.

Interested in CERTAIN Data?

If you would like to make a request for use of CERTAIN data, please contact us.

Contact us to start collaborating...

Data collected through the CERTAIN Patient Voices Project is linked to SCOAP inpatient data, creating an enriched dataset for quality improvement and future research investigations.

Download the project overview below or contact us to indicate your interest in learning more about the CERTAIN Patient Voices Project.


Patient Advisory Network Newsletters