Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
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
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