search
Back to results

Metacognitive Training With Bipolar Disorder Patients.

Primary Purpose

Bipolar Disorder

Status
Recruiting
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Metacognitive Training
Treatment as Usual
Sponsored by
University of Sao Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bipolar Disorder focused on measuring Bipolar Disorder, Theory of Mind, Social Cognition, Metacognitive Training, Cognitive Rehabilitation, Cognitive Impairment

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Diagnosis according to Diagnostic Manual of Mental Disorders (DSM-5) criteria of Bipolar Disorder type I and II.
  2. Adults, age between 18 to 55 years old.
  3. Male and/or Female
  4. Education: Must have completed 8 years of Education.
  5. Estimated Intelligence Quotient (IQ) ≥80.
  6. State of Mood: Euthymia, as to be determined with the use of Young Mania Rating Scale (YMRS) with a score of less than 8 and Montgomery-Åsberg Depression Rating Scale (MADRS) with a score of less than 12.
  7. Agreement in participation of the study, via signature obtained by the Informed Consent Form

Exclusion Criteria:

  1. Patients with visual sensorial or/and hearing disability that might prevent the correct application of the evaluation.
  2. Patients with diagnosis of a organic mental disorder
  3. Abusive use of alcohol or drugs in the last six months

Sites / Locations

  • Institute of Psychiatry, Clinic Hospital University of São PauloRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Group A: Metacognitive Training Intervention

Group B: Treatment as Usual

Arm Description

Participants of this group will undergo Metacognitive Training (MCT) in group format for the duration of 9 weeks. The intervention will be held once a week, with an estimated duration of 1-2 hours. The MCT intervention focuses on rehabilitating Social Cognition and teaching skills of interpersonal relations, as well as functional remediation aspects. We estimate a total of 26 participants in this group.

Participants of this group will continue to receive medical attention in the Bipolar Disorder Program -PROMAN- part of the University of São Paulo Medical School, although they will not be part taking in any group rehabilitation format We estimate a total of 26 participants in this group.

Outcomes

Primary Outcome Measures

Theory of Mind
After the intervention, the group that received the MCT intervention will present changes from baseline Theory of Mind (ToM) scores at 9 weeks, when compared to TAU group. ToM Scores is evaluated by using Reading the Mind in the Eyes Test (RMET). Reading the Mind in the Eyes Test (RMET) is evaluated by each correct response is awarded 1 point, resulting in a minimum score of 0 and a maximum score of 28. Incomplete responses are treated as incorrect, domain scores are scaled in a positive direction (i.e. higher scores denote higher theory of mind).

Secondary Outcome Measures

Functioning Outcome
The functional assessment scale (FAST): FAST is a standardized rating scale that is used to assess the functional impairment of individuals with bipolar disorder. The scale is designed to assess the level of functional impairment across a range of domains including autonomy, occupational functioning, cognitive functioning, financial issues, interpersonal relationships, and leisure time. The FAST is typically administered as an interview-based assessment, with the interviewer asking questions about the individual's ability to perform specific tasks and activities in each of these domains.
Social Cognition
Social cognition will be evaluated through the subtask of the CANTAB: Emotion Recognition Task.CANTAB Emotion Recognition Task is a computer-based cognitive assessment tool designed to measure an individual's ability to recognize emotions from facial expressions. The task presents a series of faces, each displaying a different emotional expression, and the participant is required to identify the emotion being displayed (such as happiness, sadness, anger, or fear) by selecting the appropriate label from a list of options.

Full Information

First Posted
June 8, 2020
Last Updated
February 27, 2023
Sponsor
University of Sao Paulo
search

1. Study Identification

Unique Protocol Identification Number
NCT04447807
Brief Title
Metacognitive Training With Bipolar Disorder Patients.
Official Title
Rehabilitating Theory of Mind: A Randomized Control Study Using Metacognitive Training in a Group Format With Bipolar Disorder Patients.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 20, 2022 (Actual)
Primary Completion Date
August 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The guiding question of this project is to evaluate the effectiveness of MCT as a form of ToM rehabilitation in patients diagnosed with BD who have deficits in this domain of social cognition. To do this, the work aims to be divided into three stages: (i) Evaluation of functionality through the FAST instrument (FAST score greater than or equal to 12 = mild impairment), to determine a subgroup of patients with deficits in functionality and evaluation scales for Montgomery & Åsberg Depression Rating Scale (MADRS) and Young Mania Rating Scale (YMRS) to verify euthymia, (ii) once these inclusion aspects have been verified, a neuropsychological assessment of hot cognition variables will be carried out, (iii) finally, the sample will be randomly divided into two groups, where one group will receive structured MCT rehabilitation and the other will continue with standard pharmacological treatment (TAU).
Detailed Description
The present study is justified by the importance of understanding, both theoretically and practically, psychotherapeutic interventions aimed at rehabilitating social cognition (SC) and specifically Theory of Mind (ToM) in individuals diagnosed with bipolar disorder (BD). ToM is an essential component for social interaction and, therefore, impairment in this area leads to problems related to interpersonal functioning. The majority of group rehabilitation interventions proposed for BD have focused primarily on cold cognitive domains or, in some cases, have only reserved one to two meetings to address strategies that integrate SC. BD is a heterogeneous disorder in terms of sociocognitive impairments and, therefore, demands more specific interventions for each individual ("personalized medicine"). Thus, the proposed intervention corresponds to a specific focus on functional rehabilitation of social cognition, with a focus on ToM, and has not yet been evaluated in this population through a randomized controlled trial. Therefore, MCT intervention may be promising as a psychotherapeutic intervention for patients who present deficits in ToM (evaluated through their functionality). Objectives General objective To evaluate the effectiveness of MCT intervention through a randomized controlled trial in euthymic patients diagnosed with BD, using Theory of Mind measures (using the RMET scale). Specific objectives To analyze the dynamics of changes between ToM and SC with the functionality scale (FAST). In this way, it is better understood if: (i) as ToM improves, FAST also improves (synchronicity)? And (ii) as SC improves, FAST also improves? (iii) Is there a correlation between the change of the two before and after intervention? To evaluate, analyze, and demonstrate, through neuropsychological assessment in a descriptive-analytical study, qualitative and quantitative aspects of Social Cognition processes in patients with BD. Material and Methods All participants will be recruited from patients regularly enrolled and clinically followed up at the Bipolar Disorder Program - PROMAN - outpatient clinic at Hospital das Clínicas, Faculty of Medicine, University of São Paulo. Participants will have access to the Informed Consent Form (ICF) for this research, and only those who agree to participate will be included in the study. This study aims to evaluate the efficacy of the MCT intervention with a specific focus on ToM and CS. To this end, the methodological proposal is divided into two stages: 01) Neuropsychological Evaluation of Cognition, ToM, and Social Cognition, and 02) MCT Intervention versus TAU. Randomization Individuals with Bipolar Disorder recruited for the research will be randomized to the MCT arm or TP arm through the Pass 22 tool using a true random algorithm. Procedures All patients who meet the described criteria and agree to participate in the study by signing the research consent form will be evaluated using the proposed neuropsychological battery. To proceed to the next stage of the project (intervention), only patients who have a deficit (represented by a score of 12 or more points) on the functionality scale (Rosa et al., 2007) will be randomly distributed (using the Pass 22 tool and a true random algorithm by a third party blinded to the research) between the experimental (MCT) and control (TP) groups. Twenty-six patients in the experimental group will participate in 9 weekly sessions following the MCT intervention proposal developed for this study. This will be based on a protocol recently developed for patients with TB by Haffner and colleagues (Haffner et al., 2018) and adapted and translated by the author of this project, Luisa de Siqueira Rotenberg, with authorization and approval for necessary modifications by the original authors. The other twenty-six patients in the control group will receive standard treatment (TP). All patients will also be accompanied by medical consultations at the Bipolar Disorder Program outpatient clinic (PROMAN, IPq-HCFMUSP), which will be scheduled according to medical evaluation. The amount of medication used and the number of medical consultations will not be limited in this study, with the aim of increasing the generalization of possible results to real clinical situations. However, these variables will be subsequently observed through medical records produced during these consultations. The neuropsychological assessment battery will be applied to all participants before the start of therapy groups and will be reapplied after the end of the intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Disorder
Keywords
Bipolar Disorder, Theory of Mind, Social Cognition, Metacognitive Training, Cognitive Rehabilitation, Cognitive Impairment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients eligible for this study will be randomized into two groups: Metacognitive Training Intervention (9 weeks) or Treatment as Usual (9 weeks).
Masking
Investigator
Allocation
Randomized
Enrollment
52 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group A: Metacognitive Training Intervention
Arm Type
Experimental
Arm Description
Participants of this group will undergo Metacognitive Training (MCT) in group format for the duration of 9 weeks. The intervention will be held once a week, with an estimated duration of 1-2 hours. The MCT intervention focuses on rehabilitating Social Cognition and teaching skills of interpersonal relations, as well as functional remediation aspects. We estimate a total of 26 participants in this group.
Arm Title
Group B: Treatment as Usual
Arm Type
Experimental
Arm Description
Participants of this group will continue to receive medical attention in the Bipolar Disorder Program -PROMAN- part of the University of São Paulo Medical School, although they will not be part taking in any group rehabilitation format We estimate a total of 26 participants in this group.
Intervention Type
Behavioral
Intervention Name(s)
Metacognitive Training
Other Intervention Name(s)
MCT
Intervention Description
MCT is a structured, interactive approach that addresses cognitive biases, social cognition, and self-esteem. This study will conducted this intervention using group format, on a weekly basis, with duration of 9 weeks total.
Intervention Type
Other
Intervention Name(s)
Treatment as Usual
Other Intervention Name(s)
TAU
Intervention Description
Patients will continue to receive medical attention in the Bipolar Disorder Program -PROMAN- part of the University of São Paulo Medical School.
Primary Outcome Measure Information:
Title
Theory of Mind
Description
After the intervention, the group that received the MCT intervention will present changes from baseline Theory of Mind (ToM) scores at 9 weeks, when compared to TAU group. ToM Scores is evaluated by using Reading the Mind in the Eyes Test (RMET). Reading the Mind in the Eyes Test (RMET) is evaluated by each correct response is awarded 1 point, resulting in a minimum score of 0 and a maximum score of 28. Incomplete responses are treated as incorrect, domain scores are scaled in a positive direction (i.e. higher scores denote higher theory of mind).
Time Frame
9 weeks.
Secondary Outcome Measure Information:
Title
Functioning Outcome
Description
The functional assessment scale (FAST): FAST is a standardized rating scale that is used to assess the functional impairment of individuals with bipolar disorder. The scale is designed to assess the level of functional impairment across a range of domains including autonomy, occupational functioning, cognitive functioning, financial issues, interpersonal relationships, and leisure time. The FAST is typically administered as an interview-based assessment, with the interviewer asking questions about the individual's ability to perform specific tasks and activities in each of these domains.
Time Frame
9 weeks
Title
Social Cognition
Description
Social cognition will be evaluated through the subtask of the CANTAB: Emotion Recognition Task.CANTAB Emotion Recognition Task is a computer-based cognitive assessment tool designed to measure an individual's ability to recognize emotions from facial expressions. The task presents a series of faces, each displaying a different emotional expression, and the participant is required to identify the emotion being displayed (such as happiness, sadness, anger, or fear) by selecting the appropriate label from a list of options.
Time Frame
9 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Diagnosis of Bipolar Disorder Type I and Type II following the DSM-V criteria, using the Mini International Neuropsychiatric Interview (MINI) (Sheehan et al., 1998). Adults between the ages of 18 and 60. Both sexes. FAST score greater than or equal to 12 (= mild impairment). Education: Completed Elementary School, as a minimum educational criterion. Estimated IQ ≥ 80. Being in euthymia, assessed through scores lower than 8 on the Young Mania Rating Scale (YMRS) and/or 12 on the Montgomery-Åsberg Depression Rating Scale (MADRS). Agreement to participate in the study by signing the Informed Consent Form (TCLE). Exclusion Criteria Subjects with complaints of visual or auditory sensory impairment that would not allow for the administration of the tests. Subjects with organic mental disorders. Subjects with a history of alcohol or drug abuse in the last six months. Treatment with electroconvulsive therapy in the last 12 months.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Beny Lafer
Phone
551126617928
Email
blafer@usp.br
First Name & Middle Initial & Last Name or Official Title & Degree
Luisa de Siqueira Rotenberg
Phone
551126617928
Email
luisarotenberg@usp.br
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Beny Lafer
Organizational Affiliation
Associate Professor of the Department of Psychiatry, USP
Official's Role
Study Director
Facility Information:
Facility Name
Institute of Psychiatry, Clinic Hospital University of São Paulo
City
São Paulo
ZIP/Postal Code
05403-903
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Luisa de Siqueira Rotenberg, PhD
Email
luisa.rotenberg@usp.br

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
28857347
Citation
Haffner P, Quinlivan E, Fiebig J, Sondergeld LM, Strasser ES, Adli M, Moritz S, Stamm TJ. Improving functional outcome in bipolar disorder: A pilot study on metacognitive training. Clin Psychol Psychother. 2018 Jan;25(1):50-58. doi: 10.1002/cpp.2124. Epub 2017 Aug 30.
Results Reference
result

Learn more about this trial

Metacognitive Training With Bipolar Disorder Patients.

We'll reach out to this number within 24 hrs