Treatment of Suicidal Recidivism in Adolescents PopulationSECURIPLANNCT02963870
The Cognitive-behavioral Approach, Standard Plan Security on Relapse Suicidal Adolescents
A study testing Security Plan in people with Treatment of Suicidal Recidivism in Adolescents Population, run by Centre Hospitalier Universitaire, Amiens at 3 sites in France.
Trial summary
The recommendation for the treatment of suicidal adolescents, Cognitive Behavioral Therapy (CBT) targeted new generation offer effective approaches to suicidal crisis and relapse prevention Read more about this study
- Who is it for?
- Ages 12 to 17 years
- Conditions the study is for
- Treatment of Suicidal Recidivism in Adolescents Population
- What is being tested?
- Security Plan
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 109 participants
- Where
- 3 sitesFrance
- Study dates
- 31 May 2017to 22 Dec 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 12 to 17 years
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Adolescents between 12 and 17, boys and girls, hospitalized for attempted suicide
- Adolescents whose parents gave informed consent and who themselves expressed their willingness to participate in research.
- Patients covered by the social insurance system
Who cannot join
- Clinical situations with self-injury without suicidal intent or suicide attempt
- mental disorders significantly impair the self-assessment questionnaire capacities: Intellectual disability, autism spectrum disorder, acute psychotic state and, psychopathy (including assessment questionnaire Frick) and the active use of alcohol and toxic (DEP teen> 20)
- have benefited a security plan before the study
- adolescents deprived of liberty.
Trial locations and contacts
3 sites in 1 country.
France3 sites
Chu Amiens Picardie
Amiens, 80000
CHU CAEN
Caen, 14000
Chu Charles Nicolle
Rouen, 76000
About this study
Official title: Randomized Controlled Trial of the Effectiveness of the Cognitive-behavioral Approach, Standard Plan Security on Relapse Suicidal Adolescents
The recommendation for the treatment of suicidal adolescents, Cognitive Behavioral Therapy (CBT) targeted new generation offer effective approaches to suicidal crisis and relapse prevention
Read the detailed description
The recommendation for the treatment of suicidal adolescents, Cognitive Behavioral Therapy (CBT) targeted new generation offer effective approaches to suicidal crisis and relapse prevention.
Since 2009, our team is engaged in a partnership between France and Quebec Interuniversity agreement concluded by a University Picardie Jules Verne-University of Montreal. In this context, two teams G4 (Amiens and Rouen) have received training in suicidal crisis, including the security plan by a university instructor and TCC Québec, Dr. Labelle. Furthermore, we complete a descriptive and prospective study of risk and protective factors for adolescent suicide in which the Quebec team of Professor Labelle contributes as an expert (sponsor: Rouen). 200 subjects were recruited on 2 years by 3 (CHU Amiens, CH Compiègne, CHU Rouen) with an assessment of recurrence at 1 year (lost rates of view = 15%). The first results highlight the central role of personal coping strategies (coping) in suicidal recurrence. We want extend this study to validate the implementation of the security plan (safety level) with suicidal adolescents. The security plan is the initial step of the TCC approach short of suicidal crisis. It is established after working with adolescents and their families (chain analysis of the suicidal crisis, coping self-evaluation and identification of support resources). Developed by Stanley B from Columbia University and adapted for francophone adolescents R Labelle and JJ Breton wrote this list those resources and coping strategies to apply in case ideation and suicidal crisis. Signed by the young person and his family, he then uses to frame the monitoring and management plan of the youth and his family environment, friendly and professional in case of suicidal crisis.
- Being tested
- Security Plan
- Keywords
- Cognitive behavioral, security plan, suicidal Recidivism in adolescents
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Security PlanOther
This study compared two groups of adolescents aged 12-17 hospitalized for TS and randomized to a group treated with the Security Plan plus the usual treatment and a group receiving standard treatment only.
| Study group | Role | What they receive |
|---|---|---|
| security plan | Experimental | groups of adolescents aged 12-17 hospitalized for TS and randomized to a group treated with security plan and the usual treatment Receives: Other: Security Plan |
| standard treatment only. | Active comparator | group receiving standard treatment only. Receives: Other: Security Plan |
What is being measured
The primary outcome is the main question the study is designed to answer.
Occurrence of suicide attempt
Occurrence of suicide attempt recurrence (documented by CNRS) during the year following randomization.
Measured: 12 months
Secondary outcomes (4)
Occurrence of relapse Suicide attempt
Occurrence of relapse Suicide attempt within 6 months of randomization.
Measured: 6 months
Observance
Observance at 6 months and 1 year using the categories used in the Giraud study
Measured: 6 months and 12 months
coping strategies of the adolescent
Compare at 1 year the evolution of coping strategies of the adolescent assessed by changes in coping scores assessed by self-questionnaire Friedenberg (ACS) from randomization to 1 year later.
Measured: 12 months
Evolution of social support perceived by the teen evaluat
Compare at 1 year evolution of social support perceived by the teen evaluated by varying the scores of self-questionnaire Sarason (SSQ6) from randomization to 1 year later.
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Nov 2016 (estimated)
- Study start31 May 2017
- Primary completion22 Dec 2023
- Study completion22 Dec 2023
Why it stopped: Recruitment difficulties
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Treatment of Suicidal Recidivism in Adolescents PopulationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 109 participants (actual)
Sponsor and investigators
- Lead sponsor
- Centre Hospitalier Universitaire, Amiens
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Jean-Marc GUILE, professor, Study director, CHU amiens-PicardieLEGRAND, Doctor, Principal investigator, CHP Philippe Pinel AmiensGERARDIN, Doctor, Principal investigator, University Hospital, RouenBALEYTE, Doctor, Principal investigator, University Hospital, CaenBernadette BAKHACHE, Doctor, Principal investigator, CH St-QuentinMaud PERCQ, Doctor, Principal investigator, EPSMD AisneVERVEL, Doctor, Principal investigator, Centre Hospitalier Intercommunal de Compiègne-Noyon
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02963870
- Sponsor's protocol ID
- PI2015_843_0009
- Acronym
- SECURIPLAN
- Status last verified
- Jun 2026
- First submitted
- 10 Nov 2016
- Last updated
- 25 Jun 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 25 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Randomized Controlled Trial of the Effectiveness of the Cognitive-behavioral Approach, Standard Plan Security on Relapse Suicidal Adolescents
- ClinicalTrials.gov ID
- NCT02963870
- Acronym / sponsor ID
- SECURIPLAN / PI2015_843_0009
- Keywords
- Cognitive behavioral, security plan, suicidal Recidivism in adolescents
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Recruitment difficulties
- Enrolment
- 109 participants (actual)
- Lead sponsor
- Centre Hospitalier Universitaire, AmiensUniversity, hospital or other
- Study start
- 31 May 2017 (actual)
- Primary completion
- 22 Dec 2023 (actual)
- Study completion
- 22 Dec 2023 (actual)
- First posted
- 15 Nov 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The recommendation for the treatment of suicidal adolescents, Cognitive Behavioral Therapy (CBT) targeted new generation offer effective approaches to suicidal crisis and relapse prevention
Detailed description
The recommendation for the treatment of suicidal adolescents, Cognitive Behavioral Therapy (CBT) targeted new generation offer effective approaches to suicidal crisis and relapse prevention.
Since 2009, our team is engaged in a partnership between France and Quebec Interuniversity agreement concluded by a University Picardie Jules Verne-University of Montreal. In this context, two teams G4 (Amiens and Rouen) have received training in suicidal crisis, including the security plan by a university instructor and TCC Québec, Dr. Labelle. Furthermore, we complete a descriptive and prospective study of risk and protective factors for adolescent suicide in which the Quebec team of Professor Labelle contributes as an expert (sponsor: Rouen). 200 subjects were recruited on 2 years by 3 (CHU Amiens, CH Compiègne, CHU Rouen) with an assessment of recurrence at 1 year (lost rates of view = 15%). The first results highlight the central role of personal coping strategies (coping) in suicidal recurrence. We want extend this study to validate the implementation of the security plan (safety level) with suicidal adolescents. The security plan is the initial step of the TCC approach short of suicidal crisis. It is established after working with adolescents and their families (chain analysis of the suicidal crisis, coping self-evaluation and identification of support resources). Developed by Stanley B from Columbia University and adapted for francophone adolescents R Labelle and JJ Breton wrote this list those resources and coping strategies to apply in case ideation and suicidal crisis. Signed by the young person and his family, he then uses to frame the monitoring and management plan of the youth and his family environment, friendly and professional in case of suicidal crisis.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| security plan | Experimental | Other: Security Plangroups of adolescents aged 12-17 hospitalized for TS and randomized to a group treated with security plan and the usual treatment |
| standard treatment only. | Active comparator | Other: Security Plangroup receiving standard treatment only. |
Who may qualify
- Ages
- 12 to 17 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (3 listed)
- Adolescents between 12 and 17, boys and girls, hospitalized for attempted suicide
- Adolescents whose parents gave informed consent and who themselves expressed their willingness to participate in research.
- Patients covered by the social insurance system
Key exclusion criteria (4 listed)
- Clinical situations with self-injury without suicidal intent or suicide attempt
- mental disorders significantly impair the self-assessment questionnaire capacities: Intellectual disability, autism spectrum disorder, acute psychotic state and, psychopathy (including assessment questionnaire Frick) and the active use of alcohol and toxic (DEP teen> 20)
- have benefited a security plan before the study
- adolescents deprived of liberty.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Security PlanThis study compared two groups of adolescents aged 12-17 hospitalized for TS and randomized to a group treated with the Security Plan plus the usual treatment and a group receiving standard treatment only. | Other | security plan, standard treatment only. |
Primary outcome
Occurrence of suicide attempt
Time frame: 12 months
Occurrence of suicide attempt recurrence (documented by CNRS) during the year following randomization.
4 secondary outcomes
Occurrence of relapse Suicide attempt
Time frame: 6 months
Observance
Time frame: 6 months and 12 months
coping strategies of the adolescent
Time frame: 12 months
Evolution of social support perceived by the teen evaluat
Time frame: 12 months
Results and safety
The study was stopped early (reason given: Recruitment difficulties). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Jun 2026.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Jean-Marc GUILE, professor study director
CHU amiens-Picardie
LEGRAND, Doctor principal investigator
CHP Philippe Pinel Amiens
GERARDIN, Doctor principal investigator
University Hospital, Rouen
3 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Security Plan in people with Treatment of Suicidal Recidivism in Adolescents Population, run by Centre Hospitalier Universitaire, Amiens at 3 sites in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 25 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 3 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study was stopped early (reason given: Recruitment difficulties). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Occurrence of suicide attempt (time frame: 12 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Jun 2026.