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NCT05523817Recruiting

Targeting Specific Brain Networks to Treat Specific Symptoms in Depression

Probing the Functional and Behavioral Impact of Precision Circuit Modulation in Neuropsychiatric Diseases

Source: ClinicalTrials.gov · Last updated 9 Oct 2026

Brief summary (registry, in English)

Repetitive transcranial magnetic stimulation (rTMS) is a way of non-invasively stimulating specific brain networks and is an established treatment for Major Depressive Disorder (MDD). This proposal will reveal network mechanisms of the therapeutic effects of rTMS by investigating how stimulating each network specifically changes network connectivity and behavior. This will be done in a highly individualized manner in depressed and healthy patients, leading to more effective and more individualized treatments for depression.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
80 (estimated)
First submitted
14 Aug 2022
Start date
12 Mar 2024
Primary completion date
31 May 2028
Lead sponsor
Massachusetts General Hospital
Diseases
Depression
NCT number
NCT05523817

What you commit to

  • Study type: Interventional
  • Planned participants: 80
  • From 12 Mar 2024 to the primary completion date, 31 May 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Implanted pacemakers, medication pumps, vagal stimulators, deep brain stimulators, or ventriculoperitoneal shunts, etc.

Other illness

  • Meeting criteria, in the past or currently, for bipolar affective disorder, hypomania or mania.
  • Meeting criteria, in the past or currently, for a primary psychotic disorder (e.g., schizophrenia).
  • Neurological conditions with known structural brain lesions, e.g., intracranial masses, multiple sclerosis.
  • Any personal history of seizures or a family history of epilepsy in a first-degree relative.
  • Severe or unstable medical illness.

Age

  • Currently pregnant, as assessed with urine pregnancy test in women of childbearing age.

Other

  • Metal in the body that is ferromagnetic or metallic injury to the eyes.
  • Substance abuse or dependence that is current and active within the last six months, as indicated by self-report (e.g., heroin, cocaine, methamphetamines).
  • Inability to meet the safety criteria for MRI scanning for any other reason.

Who the study is looking for

  • 18-65 years of age
  • Capacity to provide informed consent form to participate in the study
  • 18-65 years of age
  • Capacity to provide informed consent form to participate in the study
  • Currently in a major depressive episode. Comorbid anxiety disorders and personality disorders will be allowed provided that MDD is the primary diagnosis.

Age in the registry: 18 years to 65 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Massachusetts General Hospital
Coordinator of this site? Confirm its status
BostonUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.