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Clinical Trials/NCT03652597
NCT03652597
Completed
Not Applicable

Neuro-Cardiac-Guided Transcranial Magnetic Stimulation: a Method to Probe the Depression Network. Replication and Dose-response

Utrecht University1 site in 1 country50 target enrollmentMarch 6, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Major Depressive Disorder
Sponsor
Utrecht University
Enrollment
50
Locations
1
Primary Endpoint
Heart rate during stimulation, converted to RR intervals
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Autonomic regulation is disturbed in patients with major depressive disorder (MDD), indicated by a higher heart rate (HR) and lower heart rate variability (HRV). Moreover, the heart seems to be functionally connected via the vagus nerve (VN) to other brain structures that are dysregulated in depression, such as the subgenual anterior cingulate cortex (sgACC), and the dorsolateral prefrontal cortex (DLPFC), suggesting dysregulated network function in MDD. In line with this network dysregulation hypothesis of MDD, optimal transcranial magnetic stimulation (TMS) sites are currently thought to be those that show functional connectivity to the sgACC such as the DLPFC and multiple studies have shown that stimulation of the DLPFC, sgACC and nervus vagus decreased heart rate, suggestive of parasymphatetic action. It is hypothesized that this influence on parasympathetic activity can be used as a functional outcome measure reflecting adequate targeting of the DLPFC-sgACC network, similar to the motor evoked potential (MEP) as functional key measure for primary motor cortex stimulation. Recently, a pilot study was conducted, proposing a new functional neuronavigation method for localizing the frontal area representation of DLPFC-sgACC connectivity using HR, called: Neuro-Cardiac-Guided TMS (NCG-TMS), which is being replicated in the current study. .

Registry
clinicaltrials.gov
Start Date
March 6, 2018
End Date
May 2, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Tabitha Iseger

Principal investigator

Utrecht University

Eligibility Criteria

Inclusion Criteria

  • Between ages 18-60

Exclusion Criteria

  • No prior experience with epilepsy
  • No pregnancy
  • No metal in the head
  • No cochlear implants

Outcomes

Primary Outcomes

Heart rate during stimulation, converted to RR intervals

Time Frame: 2 weeks

Study Sites (1)

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