Researchers conducting clinical studies at Massachusetts General Hospital have access to many tools that can assist them in finding qualified study participants.

At Massachusetts General Hospital, researchers have access to many tools to assist them in finding participants for their research projects.

Rally

Rally is an online, Partners HealthCare-wide platform that supports clinical research collaborations between the public and the research community.


ResearchMatch

ResearchMatch is a national registry that can help ‘match’ you with research participants who are interested in your therapeutic area. Learn more about the Research Match researcher registration process here. Start your ResearchMatch registration process today.


Research Patient Data Registry (RPDR)

The Research Patient Data Registry (RPDR) is the central link to the Partners clinical data registry. The RPDR’s online query tool provides users with aggregate numbers of patients that meet user-defined characteristics and criteria such as diagnoses, procedures, medications and/or laboratory results.

The Data Request Wizards allow the user to ask for more detailed medical record information on the identified patient population. This process requires an approved IRB protocol. Contact the DCR with questions.


Research Study Volunteer Program (RSVP for Health)

The Research Study Volunteer Program, RSVP for Health, is a registry of individuals interested in clinical research at MGH and Brigham and Women’s Hospital. RSVP for Health users are able to search the database by disease area, age, race, gender, and ethnicity.

Once you've identified the population you'd like to contact, RSVP for Health sends potential volunteers an email containing the IRB-approved study announcement and prepares letters for those who wish to be contacted through US mail.

The identity of potential volunteers is maintained until they choose to contact you. Find more information and apply for an RSVP account.


Shared Health Research Information Network (SHRINE)

The Shared Health Research Information Network (SHRINE) helps Harvard-affiliated researchers compile large groups of well-characterized patients.

Eligible investigators may use the SHRINE web-based query tool to determine the aggregate total number of patients at participating hospitals who meet a given set of inclusion and exclusion criteria (currently demographics, diagnoses, medications, and selected laboratory values).