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Non-invasive Nerve Stimulation and Cognitive Training to Improve Cognitive Performance in Healthy Older Adults

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University of Florida

Status

Active, not recruiting

Conditions

Aging

Treatments

Behavioral: cognitive training
Device: Transcutaneous vagal nerve stimulation (tVNS)

Study type

Interventional

Funder types

Other

Identifiers

NCT04276805
IRB201902991

Details and patient eligibility

About

We need better tools to both enhance brain health and improve cognitive performance in healthy brain aging so that it can be delayed, reduced, or even reversed. The present proposal is designed to evaluate the pairing of cognitive training with a non-invasive neurostimulation technology that has shown promise in both increasing neuroplasticity and in enhancing cognitive performance, transcutaneous vagal nerve stimulation (tVNS).

Enrollment

7 patients

Sex

All

Ages

65 to 90 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy individuals willing to commit to study requirements

Exclusion criteria

  • Neurological disorders to include traumatic brain injury.
  • Evidence of dementia .
  • Major psychiatric illness
  • Unstable and chronic medical conditions.
  • MRI contraindications (e.g., pregnancy, claustrophobia, metal implants that are contraindicated for MRI).
  • Physical impairment precluding motor response or lying still or walking
  • Hearing or vision deficits that will not allow for completion of assessments

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

7 participants in 2 patient groups

tVNS group
Active Comparator group
Description:
Participants will undergo cognitive training with tVNS
Treatment:
Device: Transcutaneous vagal nerve stimulation (tVNS)
Behavioral: cognitive training
Sham group
Sham Comparator group
Description:
Participants will undergo cognitive training with earlobe sham
Treatment:
Behavioral: cognitive training

Trial contacts and locations

2

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Central trial contact

John Williamson, PhD; Brianna Akers

Data sourced from clinicaltrials.gov

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