Actively Recruiting

Phase 2
Phase 3
Age: 18Years - 65Years
All Genders
NCT05855369

Study of Chemosensory Enhancement Through Neuromodulation Training (SCENT for Long COVID)

Led by Medical University of South Carolina · Updated on 2026-04-02

145

Participants Needed

1

Research Sites

243 weeks

Total Duration

On this page

Sponsors

M

Medical University of South Carolina

Lead Sponsor

N

National Institutes of Health (NIH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Persistent smell loss that can include diminished or distorted smell function is a common symptom of long COVID syndrome. There are limited treatment options for long COVID-related smell loss. This study aims to determine the efficacy of two at-home treatments, smell training and non-invasive trigeminal nerve stimulation. This study requires participants to conduct daily at-home treatment sessions, attend three in-person study visits at the MUSC Department of Psychiatry and Behavioral Sciences, and complete electronic questionnaires over the 12-week trial, and again at the six-month timepoint. Participants in this trial may benefit directly with an improvement in sense of smell. However, participation may also help society more generally, as this study will provide new information about long COVID-related smell loss and its treatment.

CONDITIONS

Official Title

Study of Chemosensory Enhancement Through Neuromodulation Training (SCENT for Long COVID)

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Seeking treatment for COVID-related persistent smell loss (anosmia, hyposmia, phantosmia, or parosmia)
  • At least 1 month since positive SARS-CoV-2 PCR or rapid home test
  • Normal sense of smell before COVID-19 infection
  • Have not previously tried smell training or trigeminal nerve stimulation
  • Able to understand English and provide informed consent
Not Eligible

You will not qualify if you...

  • History of head injury (e.g., sports, accident, combat blast)
  • Sinonasal conditions such as upper respiratory infection, rhinosinusitis, or polyps
  • Neurological disorders including epilepsy, neurodegenerative disorders, or narcolepsy
  • Serious mental illness such as schizophrenia, bipolar disorder, or other psychotic disorders
  • Suicidal thoughts within the last month
  • Heavy cigarette smoking within the last 6 months (10 or more pack-years)
  • Use of oral or nasal steroids or other intranasal medications within the last month
  • Use of immunomodulatory medications
  • Pregnant or trying to become pregnant

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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Research Team

B

Bernadette M. Cortese, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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