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Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline
Awards & highlights
Study Summary
This trial tests if it's possible to monitor a movement disorder from a distance without an in-person visit.
Who is the study for?
This trial is for English-speaking individuals who have been on antipsychotic medication for at least 90 days. It's not suitable for those with Tardive Dyskinesia symptoms from Parkinson's, Tourette's, or Huntington disease. Participants must consent to the study and cannot have had a severe head injury in the past year, learning disorders that affect protocol adherence, or uncorrectable severe visual impairment.Check my eligibility
What is being tested?
The trial is testing 'TDtect', a method for remotely monitoring and assessing Tardive Dyskinesia—a movement disorder caused by long-term use of certain medications. The goal is to see if this tool can effectively evaluate patients outside of a clinical setting.See study design
What are the potential side effects?
Since 'TDtect' involves remote assessment tools rather than medication or invasive procedures, traditional side effects are not applicable. However, there may be indirect effects related to privacy concerns or data misinterpretation.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
AIMS Score
Trial Design
2Treatment groups
Experimental Treatment
Group I: Taking antipsychotic medication without Tardive DyskinesiaExperimental Treatment1 Intervention
Group II: Taking antipsychotic medication with Tardive DyskinesiaExperimental Treatment1 Intervention
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Who is running the clinical trial?
iRxReminderLead Sponsor
National Institute of Mental Health (NIMH)NIH
2,786 Previous Clinical Trials
2,689,399 Total Patients Enrolled
Rakesh Ranjan, M.D.Study DirectorCharak Research Center
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there opportunities for individuals to join this investigation?
"Affirmative. The portal on clinicaltrials.gov confirms that this research project, which was posted online in May of 2023, is actively searching for participants. A total of 300 individuals need to be enlisted from two different medical sites."
Answered by AI
What is the current population count of participants undertaking this medical research?
"Yes, this research is still open to new patients. According to clinicaltrials.gov, this study was first posted on May 30th 2023 and the details have since been edited as recently as August 21st of the same year. Approximately 300 participants are needed for enrolment across 2 sites."
Answered by AI
Who else is applying?
What site did they apply to?
Fermata Helath
What portion of applicants met pre-screening criteria?
Met criteria
Why did patients apply to this trial?
I've been on Ingreza with no success. I am currently on the maximum acceptable dosage of Austedo but also take Valium and Ativan multiple times daily to try and keep my movements somewhat controlled. I also get Botox injections in my face, head, and neck every 12 weeks but they wear off about 5 weeks in. There is no stability to my treatment as far as controlling symptoms.
PatientReceived 1 prior treatment
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