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A randomized pilot study which proposes to patients having suffered a traumatic event to have either only the standard care or the standard care associated with adaptated psychotrauma watch and prevention system.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Prevention algorithm | Experimental | Patient will have the current support for psychotrauma and psychotrauma prevention algorithm. |
|
| Current support for psychotrauma | Active Comparator | Patient will have the current support for psychotrauma. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| prevention algorithm | Other | a health watch adapted to stress and dissociative symptoms |
|
| Measure | Description | Time Frame |
|---|---|---|
| study acceptability rate | Number of included patient divided by number of patients to whom the study was offered. Study acceptability rate of 50% is expected. | 6 months after inclusion |
| Measure | Description | Time Frame |
|---|---|---|
| Adherence of patient to the watch | Number of patient contacted by phone having completed the scales divided by number of patient contacted. | 1 month after inclusion |
| Adherence of patient to the health watch |
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Inclusion Criteria:
Non-inclusion Criteria:
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| ID | Term |
|---|---|
| D000067073 | Psychological Trauma |
| ID | Term |
|---|---|
| D040921 | Stress Disorders, Traumatic |
| D000068099 | Trauma and Stressor Related Disorders |
| D001523 | Mental Disorders |
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| ID | Term |
|---|---|
| D059039 | Standard of Care |
| ID | Term |
|---|---|
| D019984 | Quality Indicators, Health Care |
| D011787 | Quality of Health Care |
| D006298 | Health Services Administration |
| D017530 | Health Care Quality, Access, and Evaluation |
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| Standard care | Other | Standard care for post traumatic stress disorder |
|
Number of patient contacted by phone having completed the scales divided by number of patient contacted
| 3 months after inclusion |
| Patient satisfaction (quantitatif) | A questionnaire will be completed by the patient | 3 months after inclusion |
| Patient satisfaction (qualitatif) | semi-structured interview carried-out in 3 patients volunteers (45 minutes) | 3 months after inclusion |
| Strong points of the health watch | semi-structured interview carried-out in volunteer caregivers (doctor, nurse, psychologist) | 3 months after inclusion |
| Evolution of the patient journey in experimental arm | number an percentage of patient who have changed watch | 3 months after inclusion |
| Occurrence of post-traumatic stress disorder | Evaluation by Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5). Score between 0 and 80. Score < 38 : no post-traumatic stress disorder Score = or > 38 : post-traumatic stress disorder | 3 months after inclusion |
| Complications associated with post-traumatic stress disorder | assessed by C-SSRS (Columbia-Suicide Severity Rating Scale). Assessment of suicide risk in patient. No score for this scale. | at inclusion |
| Complications associated with post-traumatic stress disorder | assessed by C-SSRS (Columbia-Suicide Severity Rating Scale). Assessment of suicide risk in patient. No score for this scale. | 3 months after inclusion |
| Complications associated with post-traumatic stress disorder | assessed by the Hospital Anxiety and Depression Scale (HADS). 1 subscore for anxiety scale (HADS-A) between 0 and 21 1 subscore for depression scale (HADS-D) between 0 and 21 Overall score between 0 and 42 HADS-A + HADS-D scores). Score < or = 7 : no symptom Score = or > 8 : symptom the higher the score, the more severe the symptoms | 3 months after inclusion |
| Complications associated with post-traumatic stress disorder | assessed by WHO Quality of life - Bref (WHOQOL Bref). This scale assessed 4 domains : physical health, mental health, social relations and the environment. Overall Score is between 26 and 130. the higher the score, the better the quality of life | 3 months after inclusion |