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Study of the Correlation Between Post-traumatic Stress Disorder and Paradoxical Sleep Behavior Disorder — TRAUMA-TCSP  

Post Traumatic Stress Disorder Clinical Trial

Official title:
Study of the Correlation Between Post-traumatic Stress Disorder and Paradoxical Sleep Behavior Disorder

Clinical Trial Summary

Post-Traumatic Stress Disorder is a psychiatric disorder that occurs after a traumatic event and is estimated to affect 5 to 12% of the general population. Around 70% of patients suffering from this disorder report sleep disorders (sleep apnea, insomnia, recurring nightmares, etc.). There are specific sleep disorders called Rapid Eye Movement (REM) sleep behavior disorders which correspond to nocturnal restlessness with sometimes violent behavior, often associated with intense dreams during a phase of sleep called REM sleep. These disorders are more frequently found in patients suffering from post-traumatic stress, such as veterans. However, the physiopathological link between these two disorders is poorly understood and studies on this subject are few in number. Through this study, the investigators wish to demonstrate whether there is a correlation between the severity of Post-Traumatic Stress Disorder and that of Rapid Eye Movement sleep behavior disorder. The main objective is to study the relationship between the severity of Post Traumatic Stress Disorder (PTSD) and the Rapid Eye Movement (REM) Sleep Behavior Disorder. This is an observational prospective study based on 4 questionnaires relating to the sleep (PSQI), the severity of the Rapid Eye Movement (REM) Sleep Behavior Disorder (REM RBDSQ, IRBD-SSS) and the severity of the Post-Traumatic Stress Disorder (PCL-5).

Clinical Trial Description

Type of study: observational prospective study Study duration : 40 min, one visit at D0 (inclusion isit) Number of center: 1 (Clermont Ferrand) Patients: 60 patients suffering from type 1 Post-traumatic Stress Disorder . Patients will be selected during their consultation, at the CUMP (Medico-Psychological Emergency Cell) of the hospital of Clermont-Ferrand. If patients accept to participate to this study, demographic and clinical data (age, sex, current treatments, medical and surgical history) will be collected. Then, they will complete 4 questionnaires : - the Rapid Eye Movement Behavior Disorder Screening Questionnaire (REM RBDSQ) - the Rapid Eye Movement Behavior Disorder symptom severity scale score (IRBDSSS) - the quality of sleep inventory (PSQI) - the Posttraumatic Stress Disorder Checklist for DSM-5 (PCL 5) ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06221865
Study type Observational
Source University Hospital, Clermont-Ferrand
Contact Lise Laclautre
Phone 334.73.754.963
Email promo_interne_drci@chu-clermontferrand.fr
Status Not yet recruiting
Phase
Start date January 15, 2024
Completion date June 1, 2026
View Details
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