Post Traumatic Stress Disorder Clinical Trial
— TEMPOOfficial title:
Psychological Sequelae After Sudden Cardiac Death in the Patient and His Relatives
Verified date | March 2023 |
Source | University Hospital, Bordeaux |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study will evaluate and describe the occurrence of Acute traumatic stress and persistence of Post Traumatic Stress Disorder (PTSD) after resuscitated sudden cardiac death (SCD) in patient and relatives present during the event. The population will be composed of 40 patients: 20 with resuscitated SCD and 20 relatives. Two interviews will be performed by a psychologist within one week after resuscitated SCD and at month 3. Questionnaire Stanford Acute Stress Reaction Questionnaire (SASRQ), Life Events Checklist for Diagnostic and Statistical Manual of Mental Disorders (DSM-5) (LEC-5) and Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5) will be filled during these interviews.
Status | Completed |
Enrollment | 45 |
Est. completion date | September 26, 2022 |
Est. primary completion date | September 26, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patients with resuscitated sudden cardiac death and/or their relative - Patients who are fluent in French - Patients who have given their 'no objection to participation to the research' - Patients of both gender over 18 years - Women with childbearing potential and effective contraception Exclusion Criteria: - People who are not able to give their 'no objection to participate to the research' - People with major cognitive disorders post sudden cardiac death - People with known psychiatric disorder - Women who are known to be pregnant or lactating - Person deprived of liberty by judicial or administrative decision - People under legal protection (under the protection of a conservator) |
Country | Name | City | State |
---|---|---|---|
France | Bordeaux University Hospital | Pessac |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Bordeaux |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Proportion of patients and relatives with PTSD at months 3 post resuscitated SCD | The percentage of patients and relatives is determined using the PCL-5 and LEC-5 questionnaire | Month 3 | |
Secondary | Proportion of patients and/or relatives with acute stress disorder | The percentage of patients and relatives is determined using the SASRQ questionnaire | Day 0 | |
Secondary | Proportion of patients and/or relatives with trauma vulnerability | The percentage of patients and/or relatives is determined using the LEC-5 included in the PCL-5 questionnaire | Month3 |
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