Survey Study for Parents
Protocol: STUDY00004266
Full Title
A Comparison of Caregiver Burden Among Parents of Children With Cerebral Palsy and Tourette Syndrome
Description
Are you the parent of a child who was diagnosed with Tourette Syndrome, or Cerebral Palsy or the parent of a child (children) with no known disability? We are hoping to learn more about the burdens caregivers face caring for children with disabilities and how that is different from the burdens of parents with children without a disability.

You will complete an online survey that takes about 20 minutes to complete. Your participation can help others to better understand caregiver burden which can help others parent in the future. This study takes place entirely online.
Compensation: No
Eligibility
Adult parents/caregivers ages 18+.
Your child is ages 5-12.
Your child has been diagnosed with Cerebral Palsy or with Tourette Syndrome *OR* your child (children) have no known disabilities.
The child must live with the primary and/or secondary caregiver.
Age Group: Adults
Principal Investigator: JANICE TONA
Contact(s)
JANICE TONA
tona@buffalo.edu
+1 716-829-6741
Want to Learn More?

Let us know how the study team can reach you. If you do not hear back within 2 business days, reach out to the study team directly at the contact information above or email ctsiresearch@buffalo.edu and someone will assist you.

Your information will be shared only with the research study team for recruitment purposes and designated CTSI personnel for project quality assurance and will remain confidential. Your information will be stored indefinitely. Should you no longer want this information to be provided in the aforementioned ways, please contact ctsiresearch@buffalo.edu.