To participate in our surveys, you must be a member of MyCP which you can join for free. After we gather some basic demographics about you or your loved one, we will present you studies that are relevant to you or your loved one. Below is a table of all of our surveys in the MyCP Community Registry and then some charts about the make up of the MyCP community. New studies are added regularly. At this time we only have surveys for people with CP and caregivers. We do not have surveys for the clinical community.

MyCP Community Registry Consent  Study Summary

Status: Active  Timeline: March 23, 2019 and beyond

Study Type: Community Registry Survey

Brief Description:

Consent for participation in CP Research Network Community Registry surveys.

Inclusion criteria: Any one in community registry

Exclusion criteria:

Principal Investigator(s): Paul Gross, University of Utah

Study Contact: paul.gross@hsc.utah.edu

Total MyCP Members: 1272
Members
  • Person/Caregiver: 1010
  • Advocate: 38
  • Provider: 173
  • Researcher: 35
  • Industry: 16

Relationship to person with CP
  • Self: 537
  • Parent: 425
  • Spouse/Partner: 7
  • Sibling: 10
  • Caregiver: 15
  • Other Relative: 16