Exploring Clinical Study Experiences of People With Post Traumatic Stress Disorder

Examination of Participation Trends and Engagement Patterns of Participants in Post Traumatic Stress Disorder Clinical Trials

Status

Not yet recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06146049

Enrollment

500

Registered

2023-11-24

Start date

2024-12-31

Completion date

2026-12-31

Last updated

2023-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Traumatic Stress Disorder

Keywords

Post Traumatic Stress Disorder

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.

Interventions

None listed

Study design

Observational model

CASE_CROSSOVER

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

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

Design outcomes

Primary

Measure	Time frame
Rate of patients who decide to enroll in a post traumatic stress disorder clinical research.	3 months
Number of post traumatic stress disorder study participants who remain in clinical study until completion.	12 months

Countries

United States

Contacts

Primary ContactMichael B Gill

bask@withpower.com4159004227

Outcome results