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UnknownNCT06011408

Remote Monitoring and Detecting of Tardive Dyskinesia for Improving Patient Outcomes

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
300 (estimated)
Sponsor
iRxReminder · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The study is being conducted to validate the feasibility of remote assessment of Tardive Dyskinesia.

Detailed description

The study is being conducted to validate the feasibility of remote assessment of Tardive Dyskinesia. Participants will all be taking an antipsychotic medication and half will have a diagnosis of Tardive Dyskinesia and half will not. Participant responses to interview questions and elements of the Abnormal Involuntary Movement Scale will be collected on video. The videos will be rated by trained observers. Machine learning methods will be used to develop an algorithm to detect abnormal movements in individuals with a known Tardive Dyskinesia diagnosis. The trained rater results will be compared to the algorithm to determine the accuracy of the algorithm.

Conditions

Interventions

TypeNameDescription
OTHERTDtectCollecting video data on abnormal movement

Timeline

Start date
2023-05-30
Primary completion
2024-11-30
Completion
2024-12-31
First posted
2023-08-25
Last updated
2024-03-12

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT06011408. Inclusion in this directory is not an endorsement.

Remote Monitoring and Detecting of Tardive Dyskinesia for Improving Patient Outcomes (NCT06011408) · Clinical Trials Directory