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NCT06146049 | NOT YET RECRUITING | Post Traumatic Stress Disorder


Exploring Clinical Study Experiences of People With Post Traumatic Stress Disorder
Sponsor:

Power Life Sciences Inc.

Brief Summary:

Participation in post traumatic stress disorder observational study serves as a crucial contribution to advancing medical knowledge and refining the care provided to individuals facing similar health challenges. The primary objective centers on a meticulous examination of trial completion rates and voluntary withdrawals within this distinct patient population.

Condition or disease

Post Traumatic Stress Disorder

Study Type : OBSERVATIONAL
Estimated Enrollment : 500 participants
Official Title : Examination of Participation Trends and Engagement Patterns of Participants in Post Traumatic Stress Disorder Clinical Trials
Actual Study Start Date : 2024-12
Estimated Primary Completion Date : 2025-12
Estimated Study Completion Date : 2026-12

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • * Diagnosis of post traumatic stress disorder
  • * No prior treatment for post traumatic stress disorder
  • * Willing and able to provide informed consent.
Exclusion Criteria
  • * Enrolled in another research study
  • * Psychiatric or behavioral illness
  • * Inability to provide written informed consent

Exploring Clinical Study Experiences of People With Post Traumatic Stress Disorder

Location Details

NCT06146049


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How to Participate

Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.

Locations


Not yet recruiting

United States, California

Power Life Sciences

San Francisco, California, United States, 94107

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