Cognitive and Immunologic Profiles of Patients With Olfactory Dysfunction After Smell Training

Part of paid clinical trials in Cleveland, Ohio.

Sponsor
The Cleveland Clinic
Study ID
NCT07681973
Status
Recruiting

Conditions

  • Chronic Rhinosinusitis (CRS)
  • Smell Loss

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • Smell Training — OTHER
    Patients experiencing loss of smell from chronic rhinosinusitis (CRS)will undergo smell training.

Study Details

A research study to assess the baseline olfactory function, mental health status, clinical severity, and immunological profile in patients with smell loss. The impact of a 3-month olfactory training program on smell function, immunological changes, and mental health in patients with smell loss will be evaluated. The primary purpose of this study is to investigate tissue and blood samples to identify molecules that may be related to smell loss, ultimately aiming to develop future treatments for this condition and correlate with cognition.

Key Dates

Start date
Dec 9, 2025
Status verified
Jun 2026
Primary completion
Dec 31, 2026
Completion
Mar 31, 2027

Study Design

Enrollment
52 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE

Arms

  • Active Comparator: Group 1: - loss of smell + CRS with nasal polyps (CRSwNP)
    Loss of smell + CRS with nasal polyps (CRSwNP)
  • Active Comparator: Group 2: - loss of smell with no CRS/no polyps - undergo 3 months of smell training
    Loss of smell + CRS with nasal polyps (CRSwNP) - undergo 3 months of smell training
  • No Intervention: Control Group 1: - no loss of smell CRS with nasal polyps (CRSwNP)
    No loss of smell CRS with nasal polyps (CRSwNP)
  • No Intervention: Control Group 2: -no loss of smell / no CRS/no polyps
    No loss of smell / no CRS/no polyps

Primary Outcome Measure

Primary Outcome Measure 1: Baseline olfactory function measured by UPSIT score [ Time Frame: Baseline ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
The Cleveland ClinicClevelandOhio44195
John O'Neill
4405062611
Hana Rosen
216-444-7018
Mohamad Chaaban (PRINCIPAL_INVESTIGATOR)

Find similar trials in Cleveland, OH

Related Studies