Studying Patterns in Patient Engagement Among Tardive Dyskinesia Patients
Launched by POWER LIFE SCIENCES INC. · Jan 12, 2024
Trial Information
Current as of June 26, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is studying how and why patients with tardive dyskinesia get involved in clinical trials. Tardive dyskinesia is a condition that causes involuntary movements, often as a side effect of certain medications. Researchers want to understand the factors that influence patient participation and how to improve the process of recruiting and keeping participants in future studies. The results of this research will be shared at conferences and in medical papers to help make clinical trials more effective for everyone involved.
To be eligible for this trial, participants must be at least 18 years old, have a diagnosis of tardive dyskinesia, and should not have received any prior treatment for the condition. They also need to be able to provide written consent to participate. Unfortunately, individuals currently enrolled in another research study or those with certain psychiatric or substance abuse disorders may not be able to join. If you participate, you can expect to share your experiences and insights, which will ultimately help shape better clinical trials for others in the future.
Gender
ALL
Eligibility criteria
- 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
About Power Life Sciences Inc.
Power Life Sciences Inc. is a forward-thinking clinical trial sponsor dedicated to advancing innovative therapeutic solutions across various medical disciplines. With a strong emphasis on scientific rigor and patient-centered approaches, the organization collaborates with leading researchers and healthcare professionals to design and execute clinical trials that prioritize safety, efficacy, and compliance. Power Life Sciences Inc. leverages cutting-edge technology and data analytics to streamline trial processes, enhance participant engagement, and accelerate the development of life-changing treatments, ultimately aiming to improve patient outcomes and contribute to the global healthcare landscape.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
San Francisco, California, United States
Patients applied
Trial Officials
Michael B Gill
Study Director
Power Life Sciences Inc.
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported