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Randomized Clinical Trial on Oxytocin and Self-Compassion Training in Borderline Personality Disorder

Phase 1
Conditions
Borderline Personality Disorder.
Therapeutic area: Psychiatry and Psychology [F] - Psychological Phenomena [F02]
Registration Number
CTIS2024-515589-15-00
Lead Sponsor
Fundacio Institut De Recerca De L'Hospital De La Santa Creu I Sant Pau
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
80
Inclusion Criteria

Diagnosis of Borderline Personality Disorder (BPD) according to two semi-structured interviews (SCID-II and DIB-R)., Ages between 18 and 50 years old., Stability of pharmacological treatment during the intervention., Previous treatment for Borderline Personality Disorder (BPD) with standard Dialectical Behavioral Therapy (DBT) or Dialectical Behavioral Therapy (DBT) skills training., High levels of self-criticism. Scores on the Inadequate Self (IS) subscale of the FSCRS-SF > 12.

Exclusion Criteria

Comorbidity with: schizophrenia, psychosis, bipolar disorder, ongoing major depressive disorder, substance dependence, organic brain disease or mental retardation according to medical examination and clinical evaluation by SCID-I., History of severe endocrinological disorders., History of Epilepsy, Renal Insufficiency or Heart Failure., Start another psychotherapy treatment in parallel., Potentially fertile women unwilling to take contraceptive measures (oral contraception, intrauterine device, partner vasectomy, tubal ligation or sexual abstinence) during the entire study period., Gestational desire or pregnancy planning during the study., Being pregnant or breastfeeding during the study., Being under medical treatment incompatible with the administration of oxytocin.

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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