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Neurostimulation
Brain Stimulation and Decision Making
Verified Trial
N/A
Waitlist Available
Led By Michael Treadway, PhD
Research Sponsored by Emory University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Are you right-handed and between the ages of 18 and 40?
For payment purposes, do you have a social security or tax identification number?
Must not have
Have you ever been diagnosed with, or think you may have, any psychological disorders?
Is there any reason you would NOT be able to undergo an MRI scan?
Timeline
Screening 1 week
Treatment 0 days
Follow Up 3 weeks
Awards & highlights
No Placebo-Only Group
Summary
This trial uses TMS and TI to stimulate specific brain areas in patients with depression and healthy individuals. The goal is to understand how these brain regions affect decision-making, especially during challenging choices. By observing changes in behavior, researchers hope to gain insights into cognitive control and decision-making in depression. TMS has shown promising results in improving cognitive functions.
Who is the study for?
This trial is for English-speaking adults with no history of mental illness. Participants should be able to complete an MRI scan and have no one in their immediate family with a history of seizures.
What is being tested?
This study determines how brain stimulation affects decision-making. It involves game-like tasks performed while undergoing Transcranial Magnetic Stimulation (TMS) or Temporal Interference stimulation (TI), focusing on the cingulate cortex's role in cognitive control during challenging choices.
What are the potential side effects?
Potential side effects from TMS/TI may include discomfort at the stimulation site, headache, lightheadedness, or seizures (rare). There also might be temporary changes in thinking patterns or mood.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowExclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Timeline
Screening ~ 1 week0 visits
Treatment ~ 0 days0 visits
Follow Up ~ 3 weeks3 visits
Screening ~ 1 week
Treatment ~ 0 days
Follow Up ~3 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Staggered Effort-Based Decision-Making Task
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Participants with Major Depressive Disorder (MDD)Experimental Treatment0 Interventions
Participants with MDD will complete computer tasks while receiving TMS/ TI
Group II: Healthy ControlActive Control1 Intervention
Participants without MDD will complete computer tasks while receiving TMS/TI
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Transcranial Magnetic Stimulation (TMS) and Transcranial Direct Current Stimulation (tDCS) are neuromodulation techniques used to treat depression by altering brain activity. TMS uses magnetic fields to induce electrical currents in specific brain regions, such as the dorsolateral prefrontal cortex, which is often underactive in depression.
This stimulation can enhance neural activity and improve mood regulation. tDCS, on the other hand, delivers a low electrical current through electrodes placed on the scalp, modulating neuronal excitability and connectivity. These treatments are important for depression patients because they offer non-invasive options that can target specific brain areas involved in mood regulation, potentially providing relief when traditional pharmacotherapy is ineffective.
New targets for rTMS in depression: a review of convergent evidence.Effect of low-frequency transcranial magnetic stimulation on an affective go/no-go task in patients with major depression: role of stimulation site and depression severity.Transcranial magnetic stimulation as a therapeutic tool in psychiatry.
New targets for rTMS in depression: a review of convergent evidence.Effect of low-frequency transcranial magnetic stimulation on an affective go/no-go task in patients with major depression: role of stimulation site and depression severity.Transcranial magnetic stimulation as a therapeutic tool in psychiatry.
Find a Location
Who is running the clinical trial?
National Institute of Mental Health (NIMH)NIH
2,917 Previous Clinical Trials
2,738,665 Total Patients Enrolled
701 Trials studying Depression
260,951 Patients Enrolled for Depression
Emory UniversityLead Sponsor
1,697 Previous Clinical Trials
2,603,718 Total Patients Enrolled
62 Trials studying Depression
9,400 Patients Enrolled for Depression
Michael Treadway, PhD4.5573 ReviewsPrincipal Investigator - Emory University
Emory University Hospital, Northside Hospital, Cartersville Medical Center, Northside Hospital - Forsyth
Harvard University, Beth Israel Deaconess Medical Center, Residency in Podiatric Surgery
2 Previous Clinical Trials
292 Total Patients Enrolled
1 Trials studying Depression
42 Patients Enrolled for Depression
5Patient Review
The doctor was very efficient in his work and I left feeling much better.
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have never had a psychiatric illness nor taken psychotropic medications.I have been diagnosed with a schizophrenia spectrum disorder.I don't have conditions that stop me from walking or running.My depression score is 11 or higher on the BDI-II.I have been diagnosed with delusional disorder.
Research Study Groups:
This trial has the following groups:- Group 1: Participants with Major Depressive Disorder (MDD)
- Group 2: Healthy Control
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 1 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 3 Weeks after you stop receiving the treatment.
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