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Suicide Sleep Monitoring (Ssleem)

Connected Sleep Recording Device for Suicidal Patients, Acceptability Study - Suicide Sleep Monitoring (Ssleem)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03068598
Acronym
SSLEEM
Enrollment
29
Registered
2017-03-03
Start date
2017-03-08
Completion date
2019-03-06
Last updated
2024-08-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suicide, Attempted

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.

Interventions

DEVICEPulseOn watch/Suunto Spartan Ultra watch

The Watch (PulseOn or Suunto Spartan Ultra) and a smartphone will be given to the patient after discharge. After a brief training on how to use the sleep tracker, patient will monitor his sleep with watch during the five nights following the discharge. All data will be transmitted directly to the smartphone. Each morning, the patient will complete a questionnaire to assess the quality of his sleep and on day 5, during a standart follow up visit, he will complete a questionnaire evaluating the acceptability of the sleep recording device.

Sponsors

University Hospital, Brest
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY
Masking
NONE

Intervention model description

The subject will receive a watch connected to a smartphone, wear at night and objectively evaluate sleep in ecological conditions

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Acceptability of the sleep recorder device in patients with previous history of suicide attempts5 days after dischargeScore obtained at the scale evaluating acceptability of the sleep recorder device during the study exit interview 5 days after inclusion

Secondary

MeasureTime frameDescription
Link between the connected record and the data collected using a self-administered questionnaire evaluating qualitatively and quantitatively sleep.5 days after dischargeSubjective evaluation of sleep by a validated questionnaire compared to the data of the sleep recording.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026