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

NCT03674580 | Completed

• 1 other identifier: CHRD1515
• Study Type: observational
• Target: 67
• Locations: 1 country
• Sites: 1

Brief Summary

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

Conditions

Suicide

Keywords

suicidal patients;psychiatry

Outcome Measures

Primary Outcomes (1)

• Mental load (calm or turbulence of the spirit) - test of the aquarium

  To assess the calm or the turbulence of the spirit of the participant, the investigator will make him take the test of the aquarium. The participant will perform an exercise to assess the load and movement of his thoughts. The participant must imagine that the aquarium reflects the content of his mind. The fish are the thoughts and the waves represent the turbulences and movements of all these thoughts. Some subjects, for example, play about with the size of the fish ("it is only a single large fish, but it takes over my entire head"), the shape of the fish ("these fish are pointed because they are bad"), scrawl (the participant scrawled on the aquarium to say that his head was overrun), the projection of feelings ("those fish there are sad") or made digressive but interesting comments ("the wavy lines carry away the fish...").

  5 days

Secondary Outcomes (2)

• Moral pain - Analog Visual Scale Battery

  5 days

• Suicidal thoughts - Analog Visual Scale Battery

  5 days

Study Arms (1)

Suicidal patients

No intervention. Follow-up of the suicidal patients

Behavioral: Follow-up of the suicidal patients

Interventions

Follow-up of the suicidal patients BEHAVIORAL

No intervention. Follow-up of the suicidal patients

Suicidal patients

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Suicidal patients followed at the Hospital Rene Dubos

You may qualify if:

• 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.

You may not qualify if:

• Not compatible health with the signing of the protocol,
• the not knowledge of the French language,
• patient who have refused the protocol.

Sponsors & Collaborators

• Hôpital NOVO: lead

Study Sites (1)

CH Rene Dubos

Pontoise, Val d'Oise, 95300, France

Location

MeSH Terms

Conditions

Suicide

Condition Hierarchy (Ancestors)

Self-Injurious Behavior; Behavioral Symptoms; Behavior

Study Officials

• BAUDOIN Thierry, PH

  Rene Dubos Hospital

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 13, 2016
• First Posted: September 17, 2018
• Study Start: May 1, 2015
• Primary Completion: September 1, 2015
• Study Completion: September 1, 2015
• Last Updated: September 17, 2018

Record last verified: 2018-09

Data Sharing

• IPD Sharing: Will not share

Locations

FR (1)