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Impact of Sending an Sms on the Rate of Telephone Responses of Subjects Contacted 3 Months After the Suicidal Act (EVAREST3)

C

Centre Psychothérapique de Nancy

Status

Not yet enrolling

Conditions

Suicide, Attempted

Treatments

Other: IMPACT OF SENDING AN SMS

Study type

Interventional

Funder types

Other

Identifiers

NCT05966077
RIPH-2022-02 (Other Identifier)
2022-A01404-39

Details and patient eligibility

About

The objective of this controlled, randomized, monocentric study is to compare the response rate of the call at 3 months of the groups with or without short message service (SMS) 48 hours before, for the subjects having benefited from the device "VigilanS Lorraine". The secondary objectives will be to appreciate the satisfaction of the subjects towards the sending of the SMS as well as to compare the delay of suicidal recidivism according to whether the subjects answered or not to the call of evaluation at 3 months of the passage to the act The main question it aims to answer is: What impact, on the rate of successful calls, could sending a text message 48 hours before the 3-month evaluation phone call have on subjects benefiting from the VigilanS device?

The participants will be divided into 2 groups:

  • 1st group: SMS sent 48 hours before the 3-month evaluation call planned in the framework of the "VigilanS Lorraine" program.
  • 2nd group (control): evaluation call at 3 months planned within the framework of the "VigilanS Lorraine" system, not preceded by an SMS 48 hours before.

The desired effect was an increase in the percentage of successful calls at 3 months, allowing for possible evaluations at 3 months in order to identify, evaluate and accompany subjects still in a suicidal crisis and thus avoid a recurrence of the act and thus a suicide.

Enrollment

250 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Having made a suicide attempt (first-time suicide or not)

  • Hosted at the Central Hospital of Nancy

  • Included in the "VigilanS Lorraine" monitoring system

  • Not presenting criteria for non-inclusion in the "VigilanS Lorraine" system, namely:

    • Guardianship
    • Held
    • Dementia
    • Not speaking French
  • Subject having received information relating to the progress of the EVAREST 3 study and having given their consent to participate

  • Subject affiliated or entitled to a social security scheme

Exclusion criteria

  • Subject without mobile phone
  • Participation in another interventional study on the prevention of suicidal recidivism
  • Subject under curatorship who was not assisted by his curator to give his consent to participate

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

250 participants in 2 patient groups

SMS
Experimental group
Description:
Sending an SMS 48 hours before the 3-month evaluation call planned as part of the VigilanS Lorraine system
Treatment:
Other: IMPACT OF SENDING AN SMS
Without SMS
No Intervention group
Description:
without Sending an SMS 48 hours before the 3-month evaluation call planned as part of the VigilanS Lorraine system

Trial contacts and locations

0

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Central trial contact

Naoual MELLOUKI BENDIM'RED, PhD; Xavier SIPP

Data sourced from clinicaltrials.gov

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