Actively Recruiting

Phase 2
Phase 3
Age: 18Years - 65Years
All Genders
ID05855369

A Randomized Controlled Trial of Smell Training and Trigeminal Nerve Stimulation in the Treatment of COVID-related Persistent Smell Loss

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

145

Participants Needed

1

Research Sites

N/A

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, including reduced or distorted smell, is a common symptom of long COVID syndrome, with limited treatment options available. This research aims to evaluate the effectiveness of two at-home treatments: smell training and non-invasive trigeminal nerve stimulation, in adults with COVID-related persistent smell loss. The study is a randomized controlled trial comparing active smell training, placebo smell training, and a combination of trigeminal nerve stimulation with active smell training. Participants will be assigned to one of three groups: one group will perform 30 minutes of trigeminal nerve stimulation once daily plus smell training twice daily, five days a week for 12 weeks; another group will do active smell training twice daily for five minutes, five days a week for 12 weeks; and the third group will receive placebo smell training twice daily for five minutes, five days a week for 12 weeks. The interventions focus on stimulating smell function through cognitive tasks and electrical stimulation. During the 12-week trial, participants will complete daily at-home treatment sessions, attend three in-person visits at the Medical University of South Carolina, and fill out electronic questionnaires. They will be followed up again at six months. Researchers will measure changes in olfactory function, perceived intensity and pleasantness of odors, quality of life related to smell, and the impact of smell loss. Secondary measures include changes in long COVID symptoms, attention, cognitive function, mood, sleep quality, daytime sleepiness, and symptoms of depression and anxiety.

CONDITIONS

Brief 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...

  • Treatment-seeking 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
  • No prior experience with 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 (e.g., upper respiratory infection, rhinosinusitis, polyps)
  • Neurological disorders (e.g., epilepsy, neurodegenerative disorders, narcolepsy)
  • Serious mental illness (e.g., schizophrenia, bipolar disorder, 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 in 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

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 12 weeks

Participants receive daily smell training, with some also receiving daily trigeminal nerve stimulation to enhance smell function. Smell training involves sniffing odorants and performing odor-related cognitive tasks or placebo activities, conducted twice daily, 5 days per week for 12 weeks.

Twice daily sessions, 5 days per week for 12 weeks

Follow-up

Duration - Up to 12 weeks

Participants are assessed for changes in smell function, long COVID symptoms, cognitive function, mood, and sleep quality at 4 and 12 weeks after starting treatment.

2 visits (at 4 weeks and 12 weeks)

Trial Site Locations

Total: 1 location

1

Medical University of South Carolina

Charleston, South Carolina, United States, 29425

Actively Recruiting

Loading map...

Research Team

B

Bernadette M. Cortese, Ph.D.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

Similar Trials

Acupuncture for Long COVID - A Pragmatic Pilot Study

Long COVID

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here