Remote Monitoring and Detecting of Tardive Dyskinesia for Improving Patient Outcomes
Status: Recruiting
Location: See all (2) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
The study is being conducted to validate the feasibility of remote assessment of Tardive Dyskinesia.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
⁃ For the non-TD group:
• Prescribed and taking an antipsychotic medication for 90-days or longer.
• Tardive Dyskinesia symptoms if present are not from Parkinsons, Tourette's syndrome, Huntington disease.
• Signed an informed consent.
• Speaks English fluently.
Locations
United States
New York
Fermata Helath
RECRUITING
Brooklyn
Ohio
Charak Research Center
RECRUITING
Garfield Heights
Contact Information
Primary
Anthony Sterns, Ph.D.
asterns@irxreminder.com
3306066675
Backup
Fred Ma, M.D., Ph.D.
fma@irxreminder.com
2164695725
Time Frame
Start Date: 2023-05-30
Estimated Completion Date: 2024-12-31
Participants
Target number of participants: 300
Treatments
Other: Taking antipsychotic medication with Tardive Dyskinesia
Other: Taking antipsychotic medication without Tardive Dyskinesia
Related Therapeutic Areas
Sponsors
Collaborators: National Institute of Mental Health (NIMH)
Leads: iRxReminder