ScentAware and OCT in MCI vs HC

University of Wisconsin (UW)

Status

Terminated

Conditions

Alzheimer Disease, Early Onset

Treatments

Device: UPSIT

Device: ScentAware

Study type

Observational

Funder types

Other

Identifiers

NCT06377241

Protocol Version 9/20/2024 (Other Identifier)

2023-1436

SMPH/OPHTHAL&VIS SCI/GEN (Other Identifier)

A536000 (Other Identifier)

Details and patient eligibility

About

The goal of this clinical trial is to learn whether a new smell test works as well as the standard clinical smell test, if there is a link between sense of smell and variations in the retina, and if these results could be used as a way to identify early stages of Alzheimer's disease. The main questions it aims to answer are:

Whether the test is as effective and reliable as the standard test
Whether there is a link between the results of the smell test and the structure of the back of the eye

Participants will:

complete a short questionnaire
have pictures of the inside of their eyes taken
perform two smell tests

Enrollment

20 patients

Sex

All

Ages

50 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Adults who are ≥ 50 and ≤ 80 years of age
Fluent in English
Able to provide written consent
Able to complete a 2.5-3-hour clinical visit, including sitting for spectral domain optical coherence tomography (SD-OCT) imaging for 30 minutes and taking cognitive and olfactory tests for 90-120 minutes
Cognitive Ability and Family History of Alzheimer's Disease/Mild Cognitive Impairment (AD/MCI):
- Cohort 1: Cognitively unimpaired, no family history of MCI or AD, and MMSE ≥ 26
- Cohort 2: Cognitively unimpaired, a positive family history of MCI or AD, and MMSE ≥ 26
- Cohort 3: An MMSE score > 22 and ≤ 25 and either
  - Clinically diagnosed MCI due to AD
  - A participant in a Wisconsin ADRC research registry with either clinically diagnosed MCI or self-reported MCI
Cohorts 1 and 2: proficient in independent use of mobile smart devices

Exclusion criteria

A history of significant ocular or nasal trauma that required medical/surgical intervention
A history of intraocular surgery except cataract extraction
A cataract extraction within 3 months prior to enrollment
Diagnosis of visually significant intraocular disease (such as late-stage age-related macular degeneration, glaucoma, or other optic nerve conditions related to brain tumor or multiple sclerosis), drug related vision loss or retinal damage
Optic neuritis on both eyes
Current use of medications that may interfere with olfactory functions
Current use of hydroxychloroquine and tamoxifen, which are known to cause retinal toxicity that may confound OCT interpretation
A history of recurrent or chronic oto-pharyngeal-laryngeal (ORL) disease (such as chronic rhinitis, nasal polyposis, or sinus disease), head trauma, toxic exposures, upper respiratory infections at time of assessment
A family history or diagnosis of other neurodegenerative diseases (e.g., multiple sclerosis, Parkinson's disease, Huntington's disease) or conditions that, in the opinion of the Investigators, may affect cognitive or olfactory functions
Olfactory loss due to COVID (current olfactory loss and/or temporary loss that has been regained)