An Advanced Digital Phenotype System Among People Suffering From Post-traumatic Stress Disorder

NCT ID: NCT03788278

Last Updated: 2019-08-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-08-20

Study Completion Date

2019-12-01

Brief Summary

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Psychiatric diagnosis is based mainly on questioning the patient and subjective impression rather than a quantitative assessment. The assessment is usually done with long time intervals between assessments and arbitrary in relation to the clinical course of the disorder. Post-traumatic stress disorder has physiological, physical, and behavioral manifestations. These changes appear as a response to different situations during the day and can be measured directly and indirectly in order to obtain an objective, quantitative and fuller picture of the severity and changes in the disorder. This is a non-interventional pilot study, using a system that collects data through wearable sensors and smartphone over a long period of time for patients suffering from PTSD and enables data analysis and characterization of a personal digital phenotype using a dedicated algorithm. Based on this pattern, the investigators will attempt to support the establishment of the PTSD diagnosis. During the course of the study, the therapeutic procedure will not be affected by the study and will be independent of the research.

Detailed Description

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Conditions

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Post-traumatic Stress Disorder

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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PTSD patients

Participants will attend clinical surveillance once every week or two. During the follow-up period, the participant will be checked as usual and will have to fill in questionnaires.

Participants will be required to wear the smart watch at all times and will need to recharge it at least once every three days.

Participants will be required to answer digital questionnaires twice a day via smartphone.

BioBeat

Intervention Type DEVICE

The watch incorporates sensors, a battery, a software system, memory components, and a communications component. the watch will be worn 24 hours a day, 7 days a week.

Non PTSD participants

Participants will attend clinical surveillance once every week or two. During the follow-up period, the participant will be checked as usual and will have to fill in questionnaires.

Participants will be required to wear the smart watch at all times and will need to recharge it at least once every three days.

Participants will be required to answer digital questionnaires twice a day via smartphone.

BioBeat

Intervention Type DEVICE

The watch incorporates sensors, a battery, a software system, memory components, and a communications component. the watch will be worn 24 hours a day, 7 days a week.

Interventions

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BioBeat

The watch incorporates sensors, a battery, a software system, memory components, and a communications component. the watch will be worn 24 hours a day, 7 days a week.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Current PTSD diagnosis based on DSM-5. We will aim to recruit patients with Clinically Administered PTSD Scale (CAPS)- 5, medium severity and up.
* A person who is being monitored by the Ministry of Defense PTSD clinic at the Sheba Medical Center.
* Proper ability to give informed consent.
* A person with a smartphone that is not hacked with an Android version 2.3 or higher (relevant to smartphones manufactured since 2011).


* Proper ability to give informed consent.
* A person with a smartphone that is not hacked with an Android version 2.3 or higher (relevant to smartphones manufactured since 2011).

Exclusion Criteria

* A person defined as a violent or suicidal person (significant events of physical violence or suicidal behavior in the past year, according to the treating psychiatrist professional opinion).
* An active or terminal oncology disease or a dialysis patient.
* A person who is not independent or reports that he/she will not meet the requirement to wear the watch, recharge it or any other requirement arising from the use of the watch.
* A person without a smartphone that is not hacked or without Android version 2.3 or higher (relevant to smartphones manufactured since 2011).


* Current mental health diagnosis.
* A person defined as a violent or suicidal person (significant events of physical violence or suicidal behavior in the past year, according to the treating psychiatrist professional opinion).
* An active or terminal oncology disease or a dialysis patient.
* A person who is not independent or reports that he/she will not meet the requirement to wear the watch, recharge it or any other requirement arising from the use of the watch.
* A person without a smartphone that is not hacked or without Android version 2.3 or higher (relevant to smartphones manufactured since 2011).
Minimum Eligible Age

18 Years

Maximum Eligible Age

120 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Nadav Goldental

OTHER

Sponsor Role lead

Responsible Party

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Nadav Goldental

Principal investigator

Responsibility Role SPONSOR_INVESTIGATOR

Other Identifiers

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SHEBA-5184-18-SMC

Identifier Type: -

Identifier Source: org_study_id

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