Suicide Sleep Monitoring (Ssleem) (SSLEEM)

Regional University Hospital Center (CHRU)

Status: Completed

Conditions: Suicide, Attempted

Treatments: Device: PulseOn watch/Suunto Spartan Ultra watch

Study type: Interventional

Funder types: Other

Identifiers

NCT03068598

SSLEEM 29BRC16.0107

Details and patient eligibility

About

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.

Enrollment: 29 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Device Feasibility

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

---

29 participants in 1 patient group

sleep monitoring

Experimental group

Description:

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.

Treatment:

Device: PulseOn watch/Suunto Spartan Ultra watch