Non-invasive Vagus Nerve Stimulation (nVNS) and Cognition in Young Adult Vapers - A Pilot Study
Vaping and Vagal Neuromodulation of Cognition
Temple University
100 participants
Mar 18, 2025
INTERVENTIONAL
Conditions
Summary
The purpose of this study is to assess the effects of non-invasive vagus nerve stimulation (nNVS) on cognitive functioning in the users of e-cigarettes or vaping products. The investigators will use a digital wellness companion product (TRUVAGA™ device) that provides mild transcutaneous nVNS. The participants will be randomized to receive either a 2-min nNVS stimulation or control stimulation in the neck region followed by completion of three cognitive tests of attention and executive function.
Eligibility
Inclusion Criteria3
- Healthy young adults
- Age range 18-25 years
- Current or prior users of e-cigarettes
Exclusion Criteria20
- Participants will be excluded from the study if they:
- Have any rash, infection, swelling, cut, soreness, drug patch, surgical scar on the neck area
- Have any implantable medical device in their body such as a pacemaker, hearing aid implant, or any other metallic/electronic device
- Have any hearing or vision problems that are not corrected
- Are pregnant or breastfeeding
- Have any learning disabilities
- Have a medical history of any of the following condition
- Meningitis
- Traumatic brain injury
- Seizure
- Syncope
- Schizophrenia
- Schizoaffective disorder
- Bulimia (eating disorder)
- Other serious neurological illness
- Have a medical history of any of the following cardiac disorder
- Carotid atherosclerosis or carotid artery disease
- Cervical vagotomy
- First degree atrioventricular block or prolonged QT interval
- Are taking any medications for to treat hypertension, arrhythmias, or are on calcium channel blockers
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Interventions
2-min transcutaneous nVNS stimulation using portable Truvaga Plus Device (electroCore Inc., Rockaway, NJ).
2-min control stimulation using portable Truvaga Plus Device (electroCore Inc., Rockaway, NJ).
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06804109