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Clinical Trials/NCT05966077
NCT05966077Not yet recruitingNot Applicable

Impact of Sending an Sms in the "Vigilans Lorraine" Monitoring System on the Rate of Telephone Responses of Subjects Contacted 3 Months After a Passage to the Suicidal Act

Centre Psychothérapique de Nancy0 sites250 target enrollmentStarted: June 1, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
250
Primary Endpoint
Percentage of successful calls during the 3 month evaluation

Study Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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
  • •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

Arms & Interventions

SMS

Experimental

Sending an SMS 48 hours before the 3-month evaluation call planned as part of the VigilanS Lorraine system

Intervention: IMPACT OF SENDING AN SMS (Other)

Without SMS

No Intervention

without Sending an SMS 48 hours before the 3-month evaluation call planned as part of the VigilanS Lorraine system

Outcomes

Primary Outcomes

Percentage of successful calls during the 3 month evaluation

Time Frame: 3 months

. A call is considered unsuccessful after 3 call attempts at 3 different times over 3 consecutive working days.

Secondary Outcomes

  • SMS delivery status:(3 months)
  • Satisfaction survey(3 months)

Investigators

Sponsor
Centre Psychothérapique de Nancy
Sponsor Class
Other
Responsible Party
Sponsor

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