Borderline Personality Disorder Clinical Trial
Official title:
Neuroimaging and Clinical Markers of Change in Borderline Personality Disorder After Metacognitive Interpersonal Therapy - Standard Approach
The present randomised clinical trial aims to assess the clinical and neurobiological changes following Metacognitive Interpersonal Therapy -standard approach (MIT-SA) compared with Clinical Structured Treatment (CST) derived from specific recommendations in APA guidelines for borderline personality disorder (BPD). The investigators will assess clinical changes in metacognitive abilities and in emotion regulation and changes in brain activation patterns at the resting state and while they view emotional pictures. A multidimensional assessment will be performed at the baseline, at 6, 12, 18 months. The investigators will take structural and functional Magnetic Resonance Images (MRIs) in MIT-Treated BPD (N=30) and CST-treated BPD (N=30) at baseline and after treatment, as well as a group of 30 healthy and unrelated volunteers that will be scanned once for comparison. Furthermore, blood analyses will be done in order to assess level of BDNF and some hormone levels (oxytocin and vasopressin) before and after treatments.
Patients will be randomly allocate to two kind of interventions: MIT-SA and CST. Patients
will be enrolled in 3 centres: Unit of Psychiatry, IRCCS San Giovanni di Dio-FBF, Brescia;
Terzo Centro di Psicoterapia Cognitiva-School of Cognitive Psychotherapy, Rome; Mental Health
Department ASL Roma G, Rome, Italy.
A multidimensional evaluation with standardized tools will assess: level of psychopathology,
depression, anger, impulsiveness, level of functioning. In particular, the assessment will
include: the Structured Clinical Interview for DSM disorder; the Difficulties in Emotion
Regulation Scale (DERS) (primary outcome); Metacognition Assessment Interview to assess
metacognitive functions. Neuropsychological assessment will assess different cognitive
domains, empathy and emotional recognition with standardized tools . Additionally, the
emotional priming paradigm to evaluate emotion processing will be included.
Data on demographics, traumatic exposure, suicide attempts, self-injury and aggression
episodes, hospitalizations, and pharmacotherapy will be collected. Structural and functional
MRI will be collected in MIT-Treated BPD (N=30) and CST-treated BPD (N=30) at baseline and
after treatment. Healthy volunteers (N=30) will be scanned once for comparison. Specific MRI
analyses:1) Whole brain (cortical thickness) analyses will be conducted to explore the
correlates of psychotherapy and treatment response. Functional connectivity studies will
consider A) activity at rest, both before and after treatment; B) functional activation in
response to standardized emotional material from the International Affective Pictures System
(IAPS). 2) Region of interest analyses: regions of particular elevance (hippocampus,
amygdale, insula) will be studied using advanced neuroimaging tools.
Blood samples will be collected in order to assess variations in levels of BDNF and some
hormones (oxytocin and vasopressin) pre- and post treatment.
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