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Exploring Clinical Study Experiences of People With Post Traumatic Stress Disorder

P

Power Life Sciences

Status

Not yet enrolling

Conditions

Post Traumatic Stress Disorder

Study type

Observational

Funder types

Industry

Identifiers

NCT06146049
65314844

Details and patient eligibility

About

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.

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

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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