Real‐World Evaluation Screening Study and Registry of Dyskinesia in Patients Taking Antipsychotic Agents
Status: | Recruiting |
---|---|
Conditions: | Neurology |
Therapuetic Areas: | Neurology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 11/24/2017 |
Start Date: | April 4, 2017 |
End Date: | August 2018 |
Contact: | Evidera RE-Kinect Registry Team |
Email: | rekinect@evidera.com |
Phone: | 1-800-242-2196 |
Prospective study to quantify the prevalence of possible tardive dyskinesia (TD) in
outpatient psychiatry practices in the United States (US), as well as to describe the
associated disease burden in a cohort of patients with one or more psychiatric disorders and
a cumulative lifetime exposure to antipsychotic medication of three months or more.
outpatient psychiatry practices in the United States (US), as well as to describe the
associated disease burden in a cohort of patients with one or more psychiatric disorders and
a cumulative lifetime exposure to antipsychotic medication of three months or more.
Inclusion Criteria:
- Patient has a cumulative lifetime exposure to antipsychotic medication of three months
or more
- Patient has a clinician confirmed diagnosis of one or more psychiatric disorder(s), as
defined in the DSM‐5
- Patient has a usual care clinic visit scheduled during the study recruitment window
(i.e. a pre‐defined 2‐week period)
- Patient is able to read and understand English
- Patient is willing and able to comply with the study requirements
Exclusion Criteria:
- Patient is unable to provide informed consent.
We found this trial at
32
sites
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