Suicide Sleep Monitoring (Ssleem)

Not Applicable

Completed

• Conditions: Suicide, Attempted
• Interventions: Device: PulseOn watch/Suunto Spartan Ultra watch

• Registration Number: NCT03068598
• Lead Sponsor: University Hospital, Brest

Brief Summary

Promising results have shown that interventions to reduce insomnia diminish suicidal ideation. A better understanding of the bidirectional mechanism between sleep disturbances and suicide behavior will allow the design of tailored interventions to prevent suicide attempts.

Significance of the proposed study for the field The aim of the present is to assess the feasibility and the acceptability of sleep tracking monitoring in a sample of suicide attempters. The investigator hypothesize that sleep monitoring using a connected object is feasable and acceptable by patients.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2017-02-22
• Study First Submitted QC: 2017-02-27
• Study First Posted: 2017-03-03
• Study Start: 2017-03-08
• Status Verified: 2018-01
• Primary Completion: 2019-03-06
• Study Completion: 2019-03-06
• Last Update Submitted: 2024-08-06
• Last Update Posted: 2024-08-07

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 29

Inclusion Criteria

• male or female, aged 18 or older,
• with suicide attempt or suicidal ideas history,
• able to understand the study,
• insured persons,
• having signed a consent form.

Exclusion Criteria

• minor patient,
• patient whose clinical status is incompatible with informed consent,
• patient tattooed on both wrists
• patient under guardianship or curatorship

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
sleep monitoring	PulseOn watch/Suunto Spartan Ultra watch	The sleep tracker and a smartphone will be given to the patient after discharge. The patient will recieve a brief training on how to use the PulseOn watch or the Suunto Spartan Ultra watch. Patient will be proposed to monitor his sleep during the five nights following the discharge.

Primary Outcome Measures

Name	Time	Method
Acceptability of the sleep recorder device in patients with previous history of suicide attempts	5 days after discharge	Score obtained at the scale evaluating acceptability of the sleep recorder device during the study exit interview 5 days after inclusion

Secondary Outcome Measures

Name	Time	Method
Link between the connected record and the data collected using a self-administered questionnaire evaluating qualitatively and quantitatively sleep.	5 days after discharge	Subjective evaluation of sleep by a validated questionnaire compared to the data of the sleep recording.

Trial Locations

Locations (1)

CHRU de Brest; 🇫🇷 Brest, France