All Participant Identification and Recruitment Resources

NephCure Kidney Network: Patient Registry Informed Consent

Published by Jordan Capizola | updated on November 7, 2017

This is an example of an Informed Consent agreement from NephCure Kidney Network. The document explains the risks and benefits of participating in research studies and lists the participant's rights. Use this as an example for creating an Informed Consent form. Read more

CENA: So You Want to Get on MOSAIC?

Published by Jordan Capizola | updated on November 7, 2017

This is a checklist for those interested in joining Mosaic. Use this to plan for a successful Mosaic-based project. Read more

PARTNERS: June 2016 Research Collaboration Intake Form

Published by Jordan Capizola | updated on November 7, 2017

This in-take form from PARTNERS PPRN is used for requesting information from PARTNERS for use in research studies. Use it as a template for your research study. Read more

AR-PoWER: May 2015 Introduction and Consent Language

Published by Jordan Capizola | updated on November 7, 2017

This is a consent form to participate in the Arthritis Patient Partnership with Comparative Effectiveness Researchers (AR-PoWER). Use this example to identify and recruit participants for your study. Read more

COPD PPRN: Privacy Policy and Security Measures for Patient Health Data

Published by Jordan Capizola | updated on November 7, 2017

This document from the COPD PPRN details the network's Privacy Policy and Data Security Measures. Use it to create your own policies and measures. Read more

PARTNERS: Volunteer Registration Questionnaire, Patient Version

Published by Jordan Capizola | updated on November 7, 2017

This questionnaire from PARTNERS PPRN is used to identify potential participants for research studies. Use it as a template to make your own questionnaire. Read more