Imaging Brain Fluids During Breathing
- Conditions
- Healthy
- Interventions
- Device: Transcutaneous vagal nerve stimulationBehavioral: Breathing task
- Registration Number
- NCT05180981
- Lead Sponsor
- Boston University Charles River Campus
- Brief Summary
This study will perform magnetic resonance imaging (MRI) measurements of hemodynamics and cerebrospinal fluid flow across breathing tasks and during breath-locked neuromodulation.
- Detailed Description
Cerebrospinal fluid (CSF) flow is essential for brain health, as it clears waste products from the brain. This study will investigate how breathing affects the flow of CSF around the brain. The investigators will perform high resolution magnetic resonance imaging (MRI) scans in participants who are breathing in specific patterns or performing simple tasks and test the effects on CSF flow. Participants will complete an imaging study visit in which the investigators will image their brain activity while they perform simple tasks, including paced breathing tasks. The participants will be split into two arms: (1) paced breathing (25 participants low resolution, 15 participants high resolution), (2) transcutaneous vagal nerve stimulation (25 participants low resolution, 15 participants high resolution). The MRI scans will take place in the 7 Tesla MRI scanner at Massachusetts General Hospital.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 80
- Adult age 18-70 years
- No ferrous metal implanted in head or body
- No history of major head trauma
- No neurological or psychiatric disorder
- Not using medication that affects brain function
- No implanted electronic devices (e.g. pacemaker)
- No implant that poses an MR contraindication
- Not pregnant, suspect they are pregnant, or seeking to become pregnant
- Not claustrophobic
- No piercings or jewelry that cannot be removed
- Does not weigh more than 250 pounds
- Normal or contact-corrected normal vision
Exclusion for transcutaneous vagus nerve stimulation (tVNS) arm:
- Conditions of skin or anatomy that affect left auricle or forehead skin and could impact placement of electrodes for tVNS or forehead stimulation
- Diagnosis of significant cardiovascular or cerebrovascular disease [e.g. congestive heart failure, stroke, cardiac conduction disorders (including: bundle branch block, heart block, long Q-T syndrome), history of asystole or non-sustained ventricular tachycardia.
- Bradycardia (defined as resting heart rate <50 bpm)
- Hypotension defined as blood pressure <90/60 mmHg
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Transcutaneous vagal nerve stimulation Breathing task Participants will receive transcutaneous vagal nerve stimulation in specific patterns. Transcutaneous vagal nerve stimulation Transcutaneous vagal nerve stimulation Participants will receive transcutaneous vagal nerve stimulation in specific patterns. Breath task Breathing task Participants will breathe in specific patterns.
- Primary Outcome Measures
Name Time Method functional magnetic resonance imaging (fMRI) signals During study (2 hours) fMRI measures of hemodynamic responses. Units: percent signal change
Cerebrospinal fluid (CSF) signals During study (2 hours) MR-based measures of CSF signals. Units: percent signal change
- Secondary Outcome Measures
Name Time Method Pulse oximetry During study ( 2 hours) Amplitude of pulse oximetry signal. Units: arbitrary (no physical units are output by this system)
Heart rate During study ( 2 hours) Heart rate variability will be calculated. Units: milliseconds (ms)
Respiratory physiology timing During study (2 hours) Breath timing. Units: Hertz (Hz)
Respiratory physiology amplitude During study (2 hours) Breath amplitude. Units: arbitrary (no physical units output by this sensor)
Trial Locations
- Locations (2)
Massachusetts General Hospital
🇺🇸Boston, Massachusetts, United States
Boston University - Charles River Campus
🇺🇸Boston, Massachusetts, United States