How to Collect a Patient Reported Outcome
Meet with one of our team members to discuss the project in detail and determine the survey/PRO requirements for your research.
- Custom Questions
- Validated Questions (SF-36, HAQ-DI)
- Longitudinal Administration
- Flare/Crisis Triggered Administration
Based on your study requirements, Sanguine will create a research protocol and informed consent form for submission and approval by the Institutional Review Board (IRB). PRO administration can be collected through a variety of verbal, physical, or electronic methods.
Upon study start, study participants are screened and consented for the survey/PRO and sample collection. Deidentified survey/PRO data is provided through a HIPAA-compliant researcher portal for real-time access.
Determine if more patient data is needed, if so, the patient can be contacted for a re-collection. Sanguine prides itself on a 95% patient retention rate when called upon for follow up visits.
The study is completed and the deidentified data is provided with your samples to be used as you see fit.
Subscribe to our Newsletter
Select what you would like to receive directly in your email