Studying Patterns in Patient Engagement Among Tardive Dyskinesia Patients
ConditionTardive Dyskinesia
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorPower Life Sciences Inc.
About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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
Disqualifiers
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 population
Tardive dyskinesia patients who are actively considering enrolling in a clinical trial for the said condition, but have not yet completed enrollment and randomization phases.
Trial design
Design model
Case-crossover
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
Rate of patients who decide to enroll in a tardive dyskinesia clinical research.
Time frame
3 months2
Number of tardive dyskinesia study participants who remain in clinical study until completion.
Time frame
12 monthsSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: