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Trial record 77 of 661 for:    SMS

Prevention of Recurrence of Suicide Attempt by Adolescent by Sending SMS (MEDIACONNEX) (MEDIACONNEX)

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ClinicalTrials.gov Identifier: NCT02762734
Recruitment Status : Recruiting
First Posted : May 5, 2016
Last Update Posted : August 26, 2019
Sponsor:
Information provided by (Responsible Party):
Central Hospital, Nancy, France

Brief Summary:

MEDIACONNEX study propose a new way of connectedness for adolescents after a suicide attempt: it is based on the sending of SMS (or mail or other new media), over a period of 6 months after their suicide attempt (SA), in order to allow them to recourse to the care more easily and so to limit the risk of suicidal recurrence. The MEDIACONNEX study will be a multicenter controlled randomized trial (East of France) and there is a funding from the Hospital. The proposal trial will test the hypothesis that adolescent suicide attempters who are receiving SMS (or mail or other new media) from the unit of care in addition to the usual care will do less SA recurrence, than those who are receiving the usual care.

The primary objective is to determine whether the use of SMS (or mail or other new media) to keep in touch with adolescent suicide attempters in addition to the usual care, compare to usual care, will reduce the delay of recurrence of suicide attempt during 6 months after the SA.


Condition or disease Intervention/treatment Phase
Suicide Other: MEDIA Not Applicable

  Show Detailed Description

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 225 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Prevention
Official Title: Multicenter Randomized Prevention Trial of Recurrence of Suicide Attempt by Adolescent by Sending SMS (MEDIACONNEX)
Actual Study Start Date : February 13, 2017
Estimated Primary Completion Date : February 2020
Estimated Study Completion Date : February 2021

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Suicide

Arm Intervention/treatment
Experimental: MEDIA
The patient will benefit of the usual care with additional text message (SMS or mail or other new media). The intervention for the group MEDIA is a "keeping in touch" intervention through sending of SMS (or mail or other new media). The patient will receive 6 SMS (or mail or other new media) during 6 months after the suicide attempt.
Other: MEDIA
The intervention for the group MEDIA is a "keeping in touch" intervention through sending of SMS (or mail or other new media). The patient will receive 6 SMS (or mail or other new media) during 6 months after the suicide attempt. The first one 7 days after the suicide attempt and the last one after 6 months. The first SMS (or mail or other new media) is sent soon after the suicide attempt because studies on adult suicide attempters underline the importance of an early start for the connectedness measures. The text message are evolving in time, and are adapted to the genre of the adolescent.

No Intervention: CLASSIC
The patient will benefit of the usual care.



Primary Outcome Measures :
  1. Delay of recurrence of suicide attempt [ Time Frame: 6 months ]
    The primary outcome is the delay of recurrence of suicide attempt during 6 months after the inclusion in the study. The recurrence and its date of occurrence will be collected by a member of the research team in each participating hospital.


Secondary Outcome Measures :
  1. Social Support [ Time Frame: 6 months ]
    Evaluation and evolution in a 6-month period after the suicide attempt of adolescent' social network using the Multidimensional Scale of Perceived Social Support (MSPSS)

  2. Quality of life [ Time Frame: 6 months ]
    Evaluation and evolution in a 6-month period after the suicide attempt of adolescent health-related quality of life using Kidscreen-27 and VSP-A

  3. Depression [ Time Frame: 6 months ]
    Evaluation and evolution in a 6-month period after the suicide attempt of adolescent' depression using Center for Epidemiologic Studies Depression Scale (CES-D)

  4. Delay of recurrence of suicide attempt [ Time Frame: 6 to 12 months after suicide attempt ]
    Delay of recurrence of suicide attempt during 6 to 12 months after the inclusion in the study. The recurrence and its date of occurrence will be collected by a member of the research team in each participating hospital.



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Ages Eligible for Study:   13 Years to 17 Years   (Child)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • be treated for a suicide attempt
  • be 13-17 years old
  • Patient living in the inter region or being able to be reorientated in the center of inclusion in case of recurrence of suicide attemps
  • have consent of patient and his/her parents to participation in research.

Exclusion Criteria:

  • The parents or/and patient who will refuse or who won't be able to accept to participate (somatic or understandability reasons),
  • Incarcerated patient
  • Those without any cell phone.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02762734


Contacts
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Contact: Fabienne LIGIER, Dr +33383154553 fabienne.ligier@cpn-laxou.com
Contact: Francis GUILLEMIN, Prof +33383852165 francis.guillemin@chru-nancy.fr

Locations
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France
CHRU Besançon Recruiting
Besançon, France, 25000
Contact: Sylvie NEZELOF, Pr.         
Hôpital de Mercy. CHR de Metz-Thionville Recruiting
Metz, France, 57085
Contact: Pascal PANNETIER, Dr.         
Chu Reims Recruiting
Reims, France, 51092
Contact: Romain BOUILLOT, Dr.         
Hopitaux Universitaires de Strasbourg Recruiting
Strasbourg, France, 67200
Contact: Julie ROLLING, Dr.         
Centre Psychothérapique de Nancy Recruiting
Vandœuvre-lès-Nancy, France, 54511
Contact: LIGIER MEDIACONNEX, Dr.         
Sponsors and Collaborators
Central Hospital, Nancy, France
Investigators
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Study Director: Fabienne LIGIER, Dr Service de Psychiatrie de l'enfant et de l'adolescent, CHRU de Nancy
Principal Investigator: Catherine PICHENÉ, Dr CPN, Unité d'Accueil des Urgences Psychiatriques
Principal Investigator: Philippe CHABERT, Dr Unité de psychopathologie de l'adolescent Service Psychothérapique pour enfants et adolescents Pôle de Psychiatrie et Santé Mentale Hôpitaux Universitaires de Strasbourg
Principal Investigator: Sylvie NEZELOF, Dr Service de Pédopsychiatrie Hôpital Jean Minjoz. CHRU de Besançon
Principal Investigator: Pascal PANNETIER, Dr Service de Psychiatrie d'Urgence et de Liaison, dans les locaux du CHR Metz-Thionville Hôpital Mercy. CHR Metz-Thionville
Principal Investigator: Jean-Michel PINOIT, Dr Service de Psychiatrie de l'enfant et de l'adolescent Hôpital d'enfants. CHU de Dijon
Principal Investigator: Anne-Catherine ROLLAND, Dr Service de Psychothérapie de l'enfant et de l'adolescent Hôpital Robert Debré. CHU de Reims

Publications:
1. World Health Organization WHO. (2011). http://www.who.int/maternal_child_adolescent/topics/adolescence/fr/ Accessed April 2016
16. Beautrais AL, Gibb SJ, Faulkner A, Mulder RT. A randomised controlled trial of a brief intervention to reduce repeat presentations to the emergency department for suicide attempt. Annals of Emergency Medicine. 2008;51:474
24. Gibson K, Cartwright C. Young people's experiences of mobile phone text counseling: Balancing connection and control. Child Youth Ser Rev. 2014;73:96-104
29. Chou Kee-lee. Assessing Chinese adolescents' social support: the multidimensional scale of perceived social support. Pers Individ Dif. 2000;28: 299-307
32. The KIDSCREEN Group Europe. The KIDSCREEN Questionnaires - Quality of life questionnaires for children and adolescents. Handbook. Lengerich: Pabst Science Publishers. 2006

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Central Hospital, Nancy, France
ClinicalTrials.gov Identifier: NCT02762734     History of Changes
Other Study ID Numbers: 2015-A00744-45
First Posted: May 5, 2016    Key Record Dates
Last Update Posted: August 26, 2019
Last Verified: August 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Plan Description: Study results will be restituted to each participant if they ask for it.

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Central Hospital, Nancy, France:
adolescent
suicide
Additional relevant MeSH terms:
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Recurrence
Suicide
Suicide, Attempted
Disease Attributes
Pathologic Processes
Self-Injurious Behavior
Behavioral Symptoms