Neural Correlates of tVNS

Functional Neural Correlates of Transcutaneous Vagal Nerve Stimulation: Effects of Anatomical Site and Waveform Parameters - An Exploratory High Resolution fMRI Study in Healthy Volunteers

Transcutaneous vagal nerve stimulation (tVNS) has been applied to a number of disease areas including visceral pain, depression, cluster headache and Alzheimer's disease. However, there is marked heterogeneity in these studies pertaining to i) the anatomical site of stimulation (neck, inner concha or tragus of ear), and ii) the waveform parameters of the stimulating impulse. This exploratory cross-sectional study will address these knowledge gaps by comparative functional neuroimaging of the neural correlates of tVNS with disparate anatomical sites and electrical waveform characteristics during rest in healthy participants.

Study Overview

• Status: Recruiting
• Conditions: fMRI; Transcutaneous Vagal Nerve Stimulation (tVNS); Nucleus of the Solitary Tract (NTS)
• Intervention / Treatment: Device: transcutaneous vagal nerve stimulation (tVNS)

• Study Type: Observational
• Enrollment (Anticipated): 16

Contacts and Locations

• Study Contact: Name: Abraham Beckers, MD; Phone Number: +31433881844; Email: ab.beckers@maastrichtuniversity.nl

Study Locations

• Netherlands
  • Maastricht, Netherlands, 6229 ER
    • Recruiting
    • Maastricht University Medical Center
    • Contact: A.B. Beckers, MD; Phone Number: 0433881844; Email: ab.beckers@maastrichtuniversity.nl
    • Principal Investigator: A.A.M. Masclee, Prof. MD. PhD
    • Sub-Investigator: D. Keszthelyi, MD. PhD
    • Sub-Investigator: A.B. Beckers, MD.
    • Sub-Investigator: D. Ivanov, PhD
    • Sub-Investigator: H.I.L. Jacobs, PhD
• United Kingdom
  • London, United Kingdom
    • Active, not recruiting
    • Queen Mary University of London. Wingate Institute of Neurogastroenterology

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 40 years (ADULT)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: Female

• Sampling Method: Probability Sample

Study Population

Female healthy volunteers aged between 18-40 years

Description

Inclusion criteria:

• Of female sex;
• Healthy participants (defined as those without a pre-existing medical comorbidity)
• Age between 18 and 40 years;
• BMI between 18 and 30 kg/m2;
• Women on oral contraceptives only
• All subjects should be right-handed.
• Inclusion will be determined on the basis of availability. Subjects should be able to attend for 2 scanning sessions.

Exclusion criteria

• Presence of metallic prostheses, pacemakers, metal clips on blood vessels, metal parts in the eye, an intrauterine device, metal braces, tattoos and/or other metal objects;
• History of major head trauma or head/brain surgery;
• History of claustrophobia;
• History of severe or chronic cardiovascular, respiratory, urogenital, gastrointestinal/ hepatic, haematological/immunologic, HEENT (head, ears, eyes, nose, throat), dermatological/connective tissue, musculoskeletal, metabolic/nutritional, endocrine, neurological/psychiatric diseases, major surgery and/or laboratory assessments which might limit participation in or completion of the study protocol;
• Use of regular medication, including vitamin and iron supplementation, except oral contraceptives, within 14 days prior to start of the study;
• Pregnancy, lactation, wish to become pregnant;
• High alcohol consumption (>15 alcoholic units consumed per week);
• Using drugs of abuse;
• Administration of investigational drugs or participation in any scientific intervention study which may interfere with this study (to be decided by the principle investigator), in the 180 days prior to the study;
• Participants unable to provide informed consent
• Participants with any systemic disease or medications that may influence the autonomic nervous system (e.g. beta-agonists or Parkinson's disease)
• Current smokers or current use of nicotine in any other way (including E-cigarettes and patches)
• History of clinical anxiety or depression, or a hospital anxiety or depression score >8
• Participants whom score 8 or more on the HADS-questionnaire at study commencement
• Patient whom have cardiovascular conduction problems
• Patient with cochlear implants
• Not meeting any of the inclusion criteria above
• Any evidence of structural brain abnormalities examined by anatomical MRI will lead to exclusion

Study Plan

How is the study designed?

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Blood oxygenation level dependent (BOLD) signal activity in the CAN during tVNS	fMRI related outcome measure	During stimulation (difference between stim on - stim off blocks)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Voxel-wise dependent BOLD signal activity in the NTS of the brainstem; somatosensory cortex; insular cortex; ACC, hypothalamus; thalamus and amygdala during auricular tVNS (parameter set 1)	fMRI related outcome measure	During stimulation (difference between stim on - stim off blocks)
Voxel-wise dependent BOLD signal activity in the NTS of the brainstem; somatosensory cortex; insular cortex; ACC, hypothalamus; thalamus and amygdala during cervical tVNS )(parameter set 1)	fMRI related outcome measure	During stimulation (difference between stim on - stim off blocks)
Voxel-wise dependent BOLD signal activity in the NTS of the brainstem; somatosensory cortex; insular cortex; ACC, hypothalamus; thalamus and amygdala during auricular tVNS (parameter set 2)	fMRI related outcome measure	During stimulation (difference between stim on - stim off blocks)
Voxel-wise dependent BOLD signal activity in the NTS of the brainstem; somatosensory cortex; insular cortex; ACC, hypothalamus; thalamus and amygdala during cervical tVNS (parameter set 2)	fMRI related outcome measure	During stimulation (difference between stim on - stim off blocks)
Voxel-wise dependent BOLD signal activity in the NTS of the brainstem; somatosensory cortex; insular cortex; ACC, hypothalamus; thalamus and amygdala during subliminal auricular tVNS (parameter set 1)	fMRI related outcome measure	During stimulation (difference between stim on - stim off blocks)
Functional connectivity / Network Connectivity of CAN regions during "active tVNS" block [to all 5 points as identified above]	fMRI related outcome measure	During stimulation (difference between stim on - stim off blocks)

Collaborators and Investigators

• Sponsor: Maastricht University Medical Center
• Collaborators: Wingate Institute of Neurogastroenterology

Study record dates

Study Major Dates

• Study Start (ACTUAL): November 1, 2020
• Primary Completion (ANTICIPATED): June 1, 2021
• Study Completion (ANTICIPATED): June 1, 2021

Study Registration Dates

• First Submitted: March 16, 2021
• First Submitted That Met QC Criteria: March 19, 2021
• First Posted (ACTUAL): March 22, 2021

Study Record Updates

• Last Update Posted (ACTUAL): March 22, 2021
• Last Update Submitted That Met QC Criteria: March 19, 2021
• Last Verified: March 1, 2021

More Information

Terms related to this study

• Other Study ID Numbers: 65751.068.2018; METC183019 (OTHER: METC aZM/UM)

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No