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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03139825
Other study ID # PI2019_843_0026
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date February 22, 2017
Est. completion date March 12, 2019

Study information

Verified date June 2023
Source Centre Hospitalier Universitaire, Amiens
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The disruption of social cognition associated with borderline personality disorder (BPD), and more specifically categorization of facial emotions, remains largely under-studied, despite the high frequency of this pathology in the clinical population. The first results differ from the observations made in adults and this confirms the relevance of studying this theme specifically in adolescence. On the cognitive level, there is a disturbance of the detection and the categorization of the facial emotions in the TPL. The characteristics of this disturbance and its possible association with an attack on the connectivity of the brain remain unknown in adolescence. No functional imaging studies are published in adolescent TPL. This pilot bimodal functional imaging study EEG-NIRS aims to collect preliminary and feasibility data to support a response to upcoming PHRC competitions and eventually offer a science thesis opportunity.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date March 12, 2019
Est. primary completion date February 22, 2018
Accepts healthy volunteers No
Gender All
Age group 14 Years to 17 Years
Eligibility Inclusion Criteria: - Adolescents 14-17 years of age with suicidal behavior and a borderline personality disorder for whom consent is obtained from parental authority, - Affiliation to Social Security Exclusion Criteria: - Intellectual disability, psychopathy, delusional or concomitant major depression

Study Design


Intervention

Other:
Exploring the feasibility of learning during cognitive tasks (EEG-NIRS)
Exploring the feasibility of the study in its aspects of recruitment and tolerability of tasks and acquisition of electrical and hemodynamic data that can be used during cognitive tasks

Locations

Country Name City State
France CHU Amiens Picardie Amiens Picardie

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Analysis by functional imaging study of the characteristics of disorders of personalities and its possible association with an attack on connectivity of the brain 3 hours
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