CAPriCORN

Patient and Community Advisory Committee (PCAC) Consultation Abstract Form

Posted on by Jodi Snare

The Chicago Area Patient-Centered Outcomes Research Network (CAPriCORN) Clinical Research Network (CRN) created this consultation abstract form for researchers to submit their study plans to the CAPriCORN Patient and Community Advisory Committee (PCAC) for the committee’s review. This template can be adapted by other advisory committees to review researchers’ study plans for input from the PCAC.

CAPriCORN is a Network Partner of PCORnet®, the National Patient-Centered Clinical Research Network. PCORnet has been developed with funding from PCORI.

Access the resource here.

CAPriCORN’s Patient/Clinician Advisory Committee (PCAC)

Posted on by Jodi Snare

This webinar features the CAPriCORN Clinical Research Network (CRN) and their Patient/Clinician Advisory Committee (PCAC). The PCAC is comprised of patients and clinicians who advise CAPriCORN on data use, research priorities, and engagement processes. Other organizations seeking to work with CAPriCORN or establish a diverse stakeholder advisory committee can use this webinar as a resource.

Access the resource here.

Patient and Clinician Advisory Committee (PCAC) Evaluation Interview Guides

Posted on by Jodi Snare

This interview guide was developed by the Chicago Area Patient-Centered Outcomes Research Network (CAPriCORN) Clinical Research Network (CRN) to hold 30-minute semi-structured (confidential) phone interviews with Patient and Clinical Advisory Committee (PCAC) members and the CAPriCORN team. Stakeholders can use this guide to assess patient engagement in their own network.

Access the resource here.

Patient and Clinical Advisory Committee (PCAC) Online Survey Form

Posted on by Jodi Snare

This survey was developed by the Chicago Area Patient-Centered Outcomes Research Network (CAPriCORN) Clinical Research Network (CRN) to evaluate the progress of the Patient and Clinical Advisory Committee (PCAC) and identify areas for improvement. Use this to develop your own engagement survey for patients, caregivers, clinicians, and other community members.

Access the resource here.