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Transcranial Direct Current Stimulation (tDCS) Neuromodulation of Executive Function Across Neuropsychiatric Populations

Not Applicable
Recruiting
Conditions
Traumatic Brain Injury
Attention Deficit Hyperactivity Disorder
Bipolar Disorder
Schizophrenia
Borderline Personality Disorder
Substance Use Disorders
Major Depressive Disorder
Interventions
Device: Transcranial Direct Current Stimulation
Registration Number
NCT04296604
Lead Sponsor
Massachusetts General Hospital
Brief Summary

In the current study, the investigators aim to understand the role of transcranial direct current stimulation (tDCS) in improving executive function across neuropsychiatric populations known to have deficits in this cognitive domain.

Detailed Description

In the current study, the investigators aim to understand the role of transcranial direct current stimulation (tDCS) in improving executive function across neuropsychiatric populations known to have deficits in this cognitive domain. The investigators will select 8 relevant diagnostic categories: traumatic brain injury, major depressive disorder, bipolar disorder, schizophrenia, attention deficit hyperactivity disorder, borderline personality disorder and substance use disorder. The study will also include a cohort of healthy controls for comparison.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
600
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Traumatic Brain InjuryTranscranial Direct Current StimulationThis group consists of individuals diagnosed with traumatic brain injury. This group will undergo three sessions of tDCS: two active sessions and one sham session. The order of the sessions is randomized.
Substance Use DisorderTranscranial Direct Current StimulationThis group consists of individuals diagnosed with substance use disorder. This group will undergo three sessions of tDCS: two active sessions and one sham session. The order of the sessions is randomized.
Healthy ControlsTranscranial Direct Current StimulationThis group consists of individuals diagnosed with healthy controls. This group will undergo three sessions of tDCS: two active sessions and one sham session. The order of the sessions is randomized.
SchizophreniaTranscranial Direct Current StimulationThis group consists of individuals diagnosed with schizophrenia. This group will undergo three sessions of tDCS: two active sessions and one sham session. The order of the sessions is randomized.
Major Depressive DisorderTranscranial Direct Current StimulationThis group consists of individuals diagnosed with major depressive disorder. This group will undergo three sessions of tDCS: two active sessions and one sham session. The order of the sessions is randomized.
Bipolar DisorderTranscranial Direct Current StimulationThis group consists of individuals diagnosed with bipolar disorder. This group will undergo three sessions of tDCS: two active sessions and one sham session. The order of the sessions is randomized.
Attention Deficit Hyperactivity DisorderTranscranial Direct Current StimulationThis group consists of individuals diagnosed with attention deficit hyperactivity disorder. This group will undergo three sessions of tDCS: two active sessions and one sham session. The order of the sessions is randomized.
Borderline Personality DisorderTranscranial Direct Current StimulationThis group consists of individuals diagnosed with borderline personality disorder. This group will undergo three sessions of tDCS: two active sessions and one sham session. The order of the sessions is randomized.
Primary Outcome Measures
NameTimeMethod
Change in N-Back TaskBaseline to Post-Treatment, 1 Week

Working Memory Task

Secondary Outcome Measures
NameTimeMethod
Change in Delayed Discounting TaskBaseline to Post-Treatment, 1 Week

Decision-Making Task

Change in Stop Signal TaskBaseline to Post-Treatment, 1 Week

Ability to Inhibit a Response Task

Change in Iowa Gambling TaskBaseline to Post-Treatment, 1 Week

Risk-Taking Task

Change in Flanker TaskBaseline to Post-Treatment, 1 Week

Attention and Inhibitory Control Task

Change in Multi-Source Interference with International Affective Picture System TaskBaseline to Post-Treatment, 1 Week

Cognitive Control During Emotional Regulation Task

Trial Locations

Locations (1)

Massachusetts General Hospital

🇺🇸

Boston, Massachusetts, United States

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