Suicide Risk Assessment by Digital Means

Suicide Clinical Trial

Official title:

Suicide Risk Assessment by Digital Means

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT04169958
• Other study ID #: SHEBA-18-5152-NG-CTIL
• Status: Not yet recruiting
• Start date: February 1, 2020
• Est. completion date: December 30, 2020

Study information

• Verified date: November 2019
• Source: The Chaim Sheba Medical Center
• Contact: NADAV GOLDENTAL, MD
• Phone: +972-503363498
• Email: nadav.gold[@]gmail.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This study is an observational study, without intervention. Using a tablet application that developed for this study. In addition, sensors are used to examine the possibility of using the system to assess the risk of suicide. It should be noted that this is a pilot study, only for a wider study involving a larger number of patients.

The system developed for the benefit of this study is based on a smartphone application installed on a standard Smartphone device that will be found in the ED or by the examiner. The system collects data from five channels one by one (the information collected from each channel is collected separately).

The data recorded from the various channels is saved on the tablet device. Then, the information transferred to the database using a cable. A statistical analysis of the data from the various channels is carried out in order to assess suicidal behavior.

After the statistical analysis, correlations will be examining between the results of the measurements and the results of the accepted questionnaires for the assessment of suicidality, which will be performed simultaneously.

Note that the duration of participation is the duration of the measurements, ie a single session that lasts up to two hours The duration of the participants in the study is determined by the time of the measurements, ie a single session lasting up to two hours.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 50
• Est. completion date: December 30, 2020
• Est. primary completion date: November 29, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Every patient who is examined in the psychiatric ward at the Sheba Medical Center

• Proper ability to give informed consent

Exclusion Criteria:

• A patient who is not independent and without an active therapist / guardian involved in the treatment

Related Conditions & MeSH terms

• Suicide

Intervention

Other:
• safe mood
A tablet application that developed for this study. In addition, sensors are used to examine the possibility of using the system to assess the risk of suicide

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
The Chaim Sheba Medical Center

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Correlations between collected digital data and suicidality rating score	Correlations between collected digital data and suicidality rating score.	1.5 years