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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:
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
Sex
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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:
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
Primary purpose
Allocation
Interventional model
Masking
250 participants in 2 patient groups
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Central trial contact
Naoual MELLOUKI BENDIM'RED, PhD; Xavier SIPP
Data sourced from clinicaltrials.gov
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