Actively Recruiting

Phase Not Applicable
Age: 16Years - 25Years
All Genders
NCT05913544

Short Integrative And Neurocognitive Therapy For Young Adults With Borderline Personality Disorder

Led by Centre Hospitalier Universitaire de Nīmes · Updated on 2025-11-24

74

Participants Needed

1

Research Sites

146 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Borderline personality disorder (BPD) is a severe, high-suicidal psychiatric disorder associated with impulsive, endangering behaviors. Young patients between 16 and 25 years old do not respond to traditional psychotherapies, which are often long and not adapted to their neurocognitive alterations linked to early trauma. The study authors hypothesize the SINTYA therapy program (one group session and one individual session weekly for 10 weeks) would reduce the level of impulsivity and clinical symptomatology (severity of the BPD; emotional regulation difficulties; dissociative symptoms; aggressiveness; ruminations; the number of self-destructive behaviors and suicidal acts; impulsive behaviors; level of suicide risk and hopelessness; the number of psychiatric hospitalizations and emergency visits for psychiatric reasons; and finally improving psychosocial functioning).

CONDITIONS

Official Title

Short Integrative And Neurocognitive Therapy For Young Adults With Borderline Personality Disorder

Who Can Participate

Age: 16Years - 25Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of Borderline Personality Disorder according to DSM-5 criteria and BPQ-80 scale
  • High severity level of BPD with a ZAN-BPD score of 18 or higher out of 36
  • Ability to understand, write, and read French
  • Able to understand the study purpose and agree to participate in evaluations
  • Signed informed consent
  • For minors, parental consent signed by at least one holder of parental authority
Not Eligible

You will not qualify if you...

  • Refusal to participate in the study
  • Presence of neurological disease or organic brain injury affecting cognitive performance
  • Intelligence quotient below 70
  • Lifetime diagnosis of schizoaffective disorder or schizophrenia
  • Previous or current participation in specific psychotherapy for BPD
  • Being legally deprived of liberty or protected by law
  • Participation in another psychotherapy study during this study
  • Participation in a drug RIPH1 study or REC study during this study
  • Currently excluded from another research protocol

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CHU de Nîmes

Nîmes, France

Actively Recruiting

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Research Team

C

Clémentine Estric

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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