Impairment of the Cognitive Flow in the Development of a Depressive Disorder and Suicidal Ideas

NCT ID: NCT03674580

Last Updated: 2018-09-17

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

COMPLETED

Total Enrollment

67 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-05-31

Study Completion Date

2015-09-30

Brief Summary

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The study consists in estimating the mental load (cognitive saturation) and the production of driving cognition to suicidal patients.

Detailed Description

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The study consists in testing two big general hypotheses:

* In the first place, that suicidals presents a mental load (cognitive saturation) and an activity pain behaviour of their space of the thought by extremely painful peripheral cognitive movements (impression that the brain is saturated of thoughts, turbulences, internal movements)
* Secondly, that suicidals produces a surplus of representations of action, such takes out that their vision of the world is saturated of a not integrable kinaesthetic imaging by the subject.

Conditions

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Suicide

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Suicidal patients

No intervention. Follow-up of the suicidal patients

Follow-up of the suicidal patients

Intervention Type BEHAVIORAL

No intervention. Follow-up of the suicidal patients

Interventions

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Follow-up of the suicidal patients

No intervention. Follow-up of the suicidal patients

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Patients followed within the framework of an ambulatory follow-up post-emergencies(post-urgent matters).
* Knowledge of the French language
* patient who have signed of the form of consent,
* patient presenting one anxio-depressive disorder(confusion) with or without suicidal episode.

Exclusion Criteria

* Not compatible health with the signing of the protocol,
* the not knowledge of the French language,
* patient who have refused the protocol.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hôpital NOVO

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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BAUDOIN Thierry, PH

Role: PRINCIPAL_INVESTIGATOR

Rene Dubos Hospital

Locations

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CH Rene Dubos

Pontoise, Val d'Oise, France

Site Status

Countries

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France

Other Identifiers

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CHRD1515

Identifier Type: -

Identifier Source: org_study_id

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