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Two programmes have been built to prevent suicidal ideation; one focuses on stress management based on cognitive and behavioural principles and the other on health promotion.
The main objective will be assessing their respective effectiveness on suicidal ideation (at least one occurrence over a 12-month period after the end of the intervention), through a randomized controlled trial, in medical students and interns.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention program - stress management program | Experimental | This intervention program on stress management is developed to prevent suicidal ideation in medical students and residents. |
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| Intervention program - health promotion program | Active Comparator | This intervention program on health promotion is developed to prevent suicidal ideation in medical students and residents. |
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| Control condition - general information | Placebo Comparator | Participants will receive weekly emails and SMSs, over the same periods of time, with general information about health except mental health, e.g. prevention of melanoma, dental care…. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Videos and/or SMS | Other | Participants assigned to one of the intervention programmes will watch videos on a website for two months then will receive SMSs for four months. |
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| Measure | Description | Time Frame |
|---|---|---|
| Suicidal ideation observed at least at one of the three assessment contacts (6, 12, 18 months). | The electronic Columbia-Suicide Severity Rating Scale (e-CSSRS) will be used to investigate suicide ideation & behaviors. Questionnaire was developped with NIMH support to screen & quantify suicide risk using consecutive questions. No score is computed when using this scale. Questionnaire investigates suicide ideation using several questions (response yes/no):
| 18 months |
| Measure | Description | Time Frame |
|---|---|---|
| Suicidal behaviour identified at least once after the intervention. | The electronic Columbia-Suicide Severity Rating Scale (e-CSSRS) will be used to investigate suicide ideation and behaviors. This questionnaire was developped with NIMH support to screen and quantify suicide risk using consecutive questions. No score is computed when using this scale. The questionnaire investigates also suicide behaviours using questions (response yes/no) on
For the present study, suicide behavior will be considered as a "yes" to any of these 4 questions. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| MARIE TOURNIER, MD, Prof | Contact | 05 56 56 17 71 | mtournier@ch-perrens.fr | |
| HELEN SAVARIEAU | Contact | 05 56 56 35 56 | hsavarieau@ch-perrens.fr |
| Name | Affiliation | Role |
|---|---|---|
| MARIE TOURNIER, MD, Prof | Centre Hospitalier CHARLES PERRENS | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Centre Hospitalier Charles PERRENS | Recruiting | Bordeaux | 33076 | France |
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| ID | Term |
|---|---|
| D059020 | Suicidal Ideation |
| ID | Term |
|---|---|
| D013405 | Suicide |
| D016728 | Self-Injurious Behavior |
| D001526 | Behavioral Symptoms |
| D001519 | Behavior |
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An open three-arm randomized controlled trial will be conducted to assess the effectiveness of two programmes of suicide prevention in fourth-year medical students and first-year interns; one based on stress management using cognitive and behavioural principles and the other on health promotion. Their respective effectiveness will be compared with a control condition. Participants will be assessed using validated questionnaires online at inclusion (before intervention) and at 6 (end of the intervention), 12, and 18 months.
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| 18 months |