CLIMAMITHE: Biomarkers of Change in BPD After Metacognitive Interpersonal Therapy-standard Approach

Sponsor
IRCCS Centro San Giovanni di Dio Fatebenefratelli (Other)
Overall Status
Completed
CT.gov ID
NCT02370316
Collaborator
(none)
78
1
2
35
2.2

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Metacognitive Interpersonal Therapy (MIT-SA)
  • Behavioral: Clinical Structured Treatment
N/A

Detailed Description

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
78 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Neuroimaging and Clinical Markers of Change in Borderline Personality Disorder After Metacognitive Interpersonal Therapy - Standard Approach
Actual Study Start Date :
Dec 1, 2015
Actual Primary Completion Date :
Nov 1, 2018
Actual Study Completion Date :
Nov 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: MIT - SA

Metacognitive Interpersonal Therapy -standard approach (MIT-SA) is a cognitive behavior-based psychotherapeutic approach that works to increase metacognitive abilities and to improve interpersonal relationships

Behavioral: Metacognitive Interpersonal Therapy (MIT-SA)
MIT-SA consists of weekly individual therapy (1 year) and weekly group sessions (six months)

Active Comparator: Clinical Structured Treatment (CST)

Clinical Structured Treatment (CST) is a structured case management and symptom-targeted medication

Behavioral: Clinical Structured Treatment
structured case management and symptom-targeted medication

Outcome Measures

Primary Outcome Measures

  1. Change in Difficulties in Emotion Regulation Scale (DERS) [6, 12, 18 months]

    Clinical changes in metacognitive abilities and in emotion regulation assessed with the Difficulties in Emotion Regulation Scale (DERS)

Secondary Outcome Measures

  1. changes in metacognitive abilities (assessed with the Metacognition Assessment Interview) [6, 12, 18 months]

    Clinical changes in metacognitive abilities assessed with the Metacognition Assessment Interview

  2. Change from Baseline in activation in the amygdala at 12 months [12 months]

    Change from Baseline in activation in the amygdala at 12 months in response to standardized emotional material from the International Affective Pictures System

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Meet DSM 5 criteria for BPD

  • Able to provide informed consent

Exclusion Criteria:
  • lifetime diagnosis of schizophrenia, schizoaffective disorder, bipolar disorder, organic mental syndromes;

  • active substance abuse or dependence in the 6 months before the enrolment;

  • concurrent psychotherapy;

  • cognitive impairment or dementia;

  • relevant neurological signs;

  • pregnancy/lactating.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Irccs Centre San Giovanni di Dio - Fatebenefratelli Brescia Italy 25125

Sponsors and Collaborators

  • IRCCS Centro San Giovanni di Dio Fatebenefratelli

Investigators

  • Principal Investigator: Roberta Rossi, PsyD, IRCCS Centro San Giovanni di Dio - FBF

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Roberta Rossi, psyD, IRCCS Centro San Giovanni di Dio Fatebenefratelli
ClinicalTrials.gov Identifier:
NCT02370316
Other Study ID Numbers:
  • GR-2011-02351347
First Posted:
Feb 24, 2015
Last Update Posted:
Feb 13, 2020
Last Verified:
Feb 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Roberta Rossi, psyD, IRCCS Centro San Giovanni di Dio Fatebenefratelli
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 13, 2020