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Boosting Psychotherapy Effects by Means of Transcranial Direct Current Stimulation (PSYCHOBOOST)

Primary Purpose

Major Depressive Disorder

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
tDCS
Sponsored by
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Major Depressive Disorder

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Ability to provide informed consent to study Ability to understand and speak the Italian language DSM-5 diagnosis of Major Depressive Disorder. Ongoing depressive episode of at least moderate intensity (HAM-D> 18) Exclusion Criteria: Previous tDCS sessions with significant side effects Positive personal history for seizures Positive family history for epileptic disease Positive personal history for neurological disease Positive personal history for head trauma with loss of consciousness Positive personal history for frequent and severe headaches Positive personal history for neurosurgical procedures Prior implantation of neurostimulation implants (DBS, VNS, etc.) Prior implantation of defibrillator or pace-maker Possibility of pregnancy or established pregnancy Substance or alcohol abuse in the past 6 months Positive personal history for schizophrenia or schizoaffective disorder Positive personal history of intellectual disability ("mental retardation") Current hospitalization Cardiac, respiratory, renal, hepatic failure, immunosuppression status

Sites / Locations

  • Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

No Intervention

Experimental

Arm Label

Active tDCS

sham tDCS and MCT

active tDCS and MCT

Arm Description

Administration of active tDCS, not followed by MCT session, but by a usual visit psychiatric follow-up

Administration of sham tDCS, followed by MCT session

Administration of active tDCS, followed by MCT session

Outcomes

Primary Outcome Measures

to evaluate the potential superiority, from the point of view of therapeutic efficacy in depression, of the approach of combined administration of tDCS and MCT, compared with interventions based tDCS alone or MCT alone.
Change in the Hamilton Depression Rating Scale will be used as parameters, during follow-up (end of treatment, 1, 3, 6 and 12 months).

Secondary Outcome Measures

To evaluate the TMS-EEG correlates of change in depressive symptomatology, correlating them with the different proposed therapeutic interventions, in a subgroup of patients recruited, in the context of a pilot study.
Change, at the end of treatment, in TMS-EEG connectivity measures, in a subgroup of patients recruited 2. Change, during follow-up (end of treatment, 1, 3, 6 and 12 months), in the scores of the following scales: Beck Depression Inventory SCL-90 Remorse Rating Scales: Penn State Worry Questionnaire Metacognition Questionnaire-30 Ruminative Response Scale Anger rumination scale Neuropsychological tests Digit span forward and backward Phonemic and semantic verbal fluency

Full Information

First Posted
May 10, 2023
Last Updated
May 10, 2023
Sponsor
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
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1. Study Identification

Unique Protocol Identification Number
NCT05866042
Brief Title
Boosting Psychotherapy Effects by Means of Transcranial Direct Current Stimulation
Acronym
PSYCHOBOOST
Official Title
Boosting Psychotherapy Effects by Means of Transcranial Direct Current Stimulation
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Completed
Study Start Date
May 1, 2021 (Actual)
Primary Completion Date
April 30, 2022 (Actual)
Study Completion Date
April 30, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

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 present study involves the administration of three types of interventions in patients with depressive episode in the context of DDM. Two-thirds of the patients will carry out a course of excitatory tDCS sessions on the left DLPFC, so as to improve attention regulation on information characterized by negative emotions and have an antidepressant effect, simultaneously with the performance of a task, the attentional training technique (ATT), aimed at achieve effective management of emotions characterized by negative emotions and which constitutes a fundamental exercise of MCT. In half of the patients who will undergo tDCS treatment, after each session of stimulation, an MCT session will be carried out. In addition, before and after the cycle of tDCS sessions and MCT sessions will be explored, in a subgroup of patients, in the context of a pilot study, the TMS- EEG of the change in depressive symptomatology, which can be correlated with the different proposed therapeutic interventions.
Detailed Description
The study - interventional, nonpharmacological, using medical devices, nonprofit - is aimed at evaluating the potential effectiveness of a multimodal intervention for the treatment of unipolar depression. The intervention involves the use of a neuro-stimulation technique, the Transcranial Direct Current Stimulation (transcranial Direct Current Stimulation - tDCS), combined with a psychotherapy intervention, metacognitive therapy (MetaCognitive Therapy, MCT). TDCS is a noninvasive neurostimulation technique involving the transcranial application of a low-amperage electric current at a region of the cerebral cortex involved in the pathogenesis of major depression, the dorsolateral prefrontal cortex. It has been demonstrated how such stimulation has a neuromodulating effect on synaptic plasticity, with efficacy in unipolar major depression. The technique also has a good safety, as it is not associated with major side effects. MCT is based on the metacognitive model, according to which psychopathological processes are consequent to a cognitive style characterized by repetitive forms of thinking (such as rumination) and maladaptive behaviors such as avoidance and thought suppression. The MCT, through attention training techniques, detached mindfulness and behavioral interventions on metacognitions, has shown effectiveness in major depressive disorder comparable to that of psychotherapeutic interventions considered, within psychotherapies, to be first-line such as cognitive-behavioral therapy. The experimental design will be that of a randomized, double-blind study with three arms of treatment, each consisting of 8 sessions, involving the administration of 1) the neurostimulation intervention (tDCS), 2) of the psychotherapeutic intervention alone (MCT), 3) of both techniques in consecution (tDCS-MCT). This design is aimed at evaluating a potential additive/synergistic effect of the two interventions when combined. During the tDCS sessions, each lasting 20 minutes, the patient will apply the technique of attention training, aimed at further activating the region stimulated by neurostimulation, so as to so as to amplify the plasticity stimulated by tDCS, achieving a synergistic effect. To follow, a 40-minute MCT session will be carried out. The effectiveness of these interventions will be assessed by heteroadministered and self-administered at time zero, after treatment, at two follow-ups of 6 and 12 months. Before and after the treatment cycle (tDCS sessions and MCT sessions), a subgroup of patients will be explored, in the context of a pilot study, the TMS-EEG correlates of the change in symptomatology depression, which can be correlated with the different proposed therapeutic interventions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depressive Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
54 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Active tDCS
Arm Type
Experimental
Arm Description
Administration of active tDCS, not followed by MCT session, but by a usual visit psychiatric follow-up
Arm Title
sham tDCS and MCT
Arm Type
No Intervention
Arm Description
Administration of sham tDCS, followed by MCT session
Arm Title
active tDCS and MCT
Arm Type
Experimental
Arm Description
Administration of active tDCS, followed by MCT session
Intervention Type
Device
Intervention Name(s)
tDCS
Intervention Description
TDCS is a noninvasive neurostimulation technique involving the transcranial application of a low-amperage electric current at a region of the cerebral cortex involved in the pathogenesis of major depression, the dorsolateral prefrontal cortex. In healthy subjects, the administration of excitatory tDCS on the left DLPFC improves the regulation of attention on information characterized by negative emotions, as does the administration of inhibitory tDCS on the DLPFC Right tDCS produces small changes in the neuronal membrane potential, thus increasing or decreasing the excitability of the stimulated tissue. Simultaneous administration to behavioral tasks designed to activate the stimulated cortical region should achieve a synergistic, amplifying the plasticity stimulated by the task.
Primary Outcome Measure Information:
Title
to evaluate the potential superiority, from the point of view of therapeutic efficacy in depression, of the approach of combined administration of tDCS and MCT, compared with interventions based tDCS alone or MCT alone.
Description
Change in the Hamilton Depression Rating Scale will be used as parameters, during follow-up (end of treatment, 1, 3, 6 and 12 months).
Time Frame
end of treatment, 1, 3, 6 and 12 months
Secondary Outcome Measure Information:
Title
To evaluate the TMS-EEG correlates of change in depressive symptomatology, correlating them with the different proposed therapeutic interventions, in a subgroup of patients recruited, in the context of a pilot study.
Description
Change, at the end of treatment, in TMS-EEG connectivity measures, in a subgroup of patients recruited 2. Change, during follow-up (end of treatment, 1, 3, 6 and 12 months), in the scores of the following scales: Beck Depression Inventory SCL-90 Remorse Rating Scales: Penn State Worry Questionnaire Metacognition Questionnaire-30 Ruminative Response Scale Anger rumination scale Neuropsychological tests Digit span forward and backward Phonemic and semantic verbal fluency
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Ability to provide informed consent to study Ability to understand and speak the Italian language DSM-5 diagnosis of Major Depressive Disorder. Ongoing depressive episode of at least moderate intensity (HAM-D> 18) Exclusion Criteria: Previous tDCS sessions with significant side effects Positive personal history for seizures Positive family history for epileptic disease Positive personal history for neurological disease Positive personal history for head trauma with loss of consciousness Positive personal history for frequent and severe headaches Positive personal history for neurosurgical procedures Prior implantation of neurostimulation implants (DBS, VNS, etc.) Prior implantation of defibrillator or pace-maker Possibility of pregnancy or established pregnancy Substance or alcohol abuse in the past 6 months Positive personal history for schizophrenia or schizoaffective disorder Positive personal history of intellectual disability ("mental retardation") Current hospitalization Cardiac, respiratory, renal, hepatic failure, immunosuppression status
Facility Information:
Facility Name
Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico
City
Milan
State/Province
MI
ZIP/Postal Code
20100
Country
Italy

12. IPD Sharing Statement

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Boosting Psychotherapy Effects by Means of Transcranial Direct Current Stimulation

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