Actively Recruiting

Phase Not Applicable
Age: 45Years - 80Years
All Genders
NCT07517237

taVNS + CCT for Neurocognitive Rehab

Led by Medical University of South Carolina · Updated on 2026-04-08

20

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

Sponsors

M

Medical University of South Carolina

Lead Sponsor

E

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to investigate whether combining transcutaneous auricular vagus nerve stimulation (taVNS) with computerized cognitive training might help improve thinking abilities and mood. Participants will self-administer these treatment in their homes and undergo pre- and post-treatment assessments of thinking abilities and mood and brain MRIs.

CONDITIONS

Official Title

taVNS + CCT for Neurocognitive Rehab

Who Can Participate

Age: 45Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ages 45 to 80 years inclusive
  • Adequate motor function of dominant hand and verbal abilities to complete assessments
  • Access to reliable Wi-Fi and a Bluetooth-enabled mobile phone or tablet with internet
  • Self-reported cognitive changes lasting 6 months or more with concern or impact on daily life
  • Stable dose of medication(s) for at least 4 weeks before enrollment and expected to remain stable during study
Not Eligible

You will not qualify if you...

  • Prior diagnosis of Mild Cognitive Impairment, Dementia, or Mild/Major Neurocognitive Disorder
  • Contraindications to taVNS such as history of seizures or ear trauma
  • Contraindications to MRI including ferromagnetic implants or claustrophobia
  • Acute, unstable, or severe neurological, medical, or psychiatric conditions interfering with safe participation or assessments
  • Participation in another clinical trial or investigational treatment within last 30 days affecting cognition or mood
  • Positive pregnancy test in females still menstruating within past 12 months

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Medical University of South Carolina

Charleston, South Carolina, United States, 29425

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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