Identifying specific features of complex post-traumatic stress disorder
Identification of the Clinical Specificities of Complex Posttraumatic Stress Disorder
This study is trying to find out what makes complex post-traumatic stress disorder different from regular PTSD to help create better treatments for those who have it.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 372 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital, Tours Academic / other |
| Locations | 1 site (Tours) |
| Trial ID | NCT05592652 on ClinicalTrials.gov |
What this trial studies
This study aims to identify the clinical specificities of complex post-traumatic stress disorder (C-PTSD) compared to simple PTSD. It addresses the current lack of data on the characterization of PTSD, which is essential for establishing its validity as a distinct disorder. By focusing on the relationship between diagnosis and treatment, the study seeks to develop more effective treatment strategies tailored to the unique psychopathology of patients with C-PTSD. The methodology involves conducting surveys to gather relevant data from participants.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who have been diagnosed with complex post-traumatic stress disorder.
Not a fit: Patients with current or past psychotic disorders, neurological diseases, or significant head trauma may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment strategies for patients suffering from complex post-traumatic stress disorder.
How similar studies have performed: While there is limited data on the specificities of complex PTSD, similar studies have shown promise in understanding PTSD as a distinct disorder, making this approach both relevant and necessary.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria Patient : * Age ≥ 18 years * Free, informed and signed consent * Affiliated to a social security scheme Inclusion Criteria volonteer : * Age ≥ 18 years * Free, informed and signed consent * Affiliated to a social security scheme Exclusion Criteria (patient and volonteer): * Under legal protection (curatorship, guardianship, safeguard of justice) * Present a former or current psychotic disorder, a former or current neurological disease, a history of head trauma (loss of consciousness of more than 10 minutes)
Where this trial is running
Tours
- UHTours — Tours, France (Recruiting)
Study contacts
- Study coordinator: Wissam ELHAGE, Pr
- Email: wissam.elhage@univ-tours.fr
- Phone: 033247478043
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.