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Studying Patterns in Patient Engagement Among Tardive Dyskinesia Patients

P

Power Life Sciences

Status

Not yet enrolling

Conditions

Tardive Dyskinesia

Study type

Observational

Funder types

Industry

Identifiers

NCT06218719
57697757

Details and patient eligibility

About

The statistical analysis of the collected data aims to reveal the many factors that influence patient involvement in clinical trials. Findings will be disseminated through conferences and scholarly papers to benefit all parties participating in clinical trials.

These findings will help to shape the design of future clinical trials for people with tardive dyskinesia, as well as enhance recruiting techniques and retention rates.

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of tardive dyskinesia
  • Aged ≥ 18 years old and ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
  • No prior treatment for tardive dyskinesia

Exclusion criteria

  • Enrolled in another research study
  • Inability to provide written informed consent
  • Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial

Trial design

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Michael B Gill

Data sourced from clinicaltrials.gov

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