Actively Recruiting

Phase Not Applicable
Age: 18Years - 55Years
All Genders
NCT06772831

Cognitive Reappraisal Training for Borderline Personality (BPD)

Led by Icahn School of Medicine at Mount Sinai · Updated on 2025-12-03

130

Participants Needed

1

Research Sites

141 weeks

Total Duration

On this page

Sponsors

I

Icahn School of Medicine at Mount Sinai

Lead Sponsor

W

William Marsh Rice University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Previous work by the group convinced the researchers to pursue development of focused cognitive reappraisal training as a novel approach to treatment of BPD, either as stand-alone treatment or in concert with evidence-based treatments of BPD. The present proposal aims to refine and test a proposed clinical intervention for BPD patients, training in reappraisal-by-distancing, in terms of its ability to influence hypothesized neural and behavioral targets and, once that is established, to demonstrate its ability improve clinically relevant outcome measures.

CONDITIONS

Official Title

Cognitive Reappraisal Training for Borderline Personality (BPD)

Who Can Participate

Age: 18Years - 55Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Medically healthy men and women with Borderline Personality Disorder who are mentally competent and give informed voluntary written consent.
  • Participants will be between the ages of 18 and 55.
  • Inclusion includes both genders and all racial/ethnic groups to reflect previous recruitment.
  • Participants with comorbid avoidant personality disorder are included.
  • Participants with PTSD are included if they are not actively experiencing symptoms.
Not Eligible

You will not qualify if you...

  • Participants meeting criteria for Schizotypal Personality Disorder are excluded.
  • Participants currently meeting criteria for Major Depressive Disorder are excluded.
  • Participants meeting criteria for present PTSD, bipolar I disorder, schizophrenia, schizoaffective disorder, substance use disorder within the past 6 months, organic mental syndromes, head trauma, schizotypal personality disorder, CNS neurological disease, or seizure disorder are excluded.
  • Participants with substance use disorder more than 6 months prior to enrollment may be included.
  • Participants with pacemakers, surgical clips, metallic implants, or shrapnel fragments contraindicating MRI are excluded.
  • Pregnant women are excluded.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Icahn School of Medicine at Mount Sinai

New York, New York, United States, 10029

Actively Recruiting

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Research Team

H

Harold W Koenigsberg, MD

CONTACT

B

Brian B Kang, BA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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