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Cohort 2 for Alzheimer's Disease
N/A
Recruiting
Led By Sanbrita Mondal, OD
Research Sponsored by University of Wisconsin, Madison
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up one month post baseline
Awards & highlights
Study Summary
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
Eligible Conditions
- Alzheimer's Disease
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ one month post baseline
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~one month post baseline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Compare ScentAware test results conducted with support from clinical staff to the test results when ScentAware test was self-administered independently
Compare UPSIT test results conducted with support from clinical staff to the test results when ScentAware test was self-administered independently
Compare test scores of ScentAware olfactory test to the scores of the University of Pennsylvania Smell Identification Test (UPSIT) olfactory test in a clinical setting
Secondary outcome measures
Compare baseline ScentAware test scores between cohorts
Compare baseline ScentAware test scores to the ganglion cell layer (GCL) thickness
Compare baseline ScentAware test scores to the retinal nerve fiber layer (RNFL) thickness
+3 moreTrial Design
3Treatment groups
Experimental Treatment
Group I: Cohort 3Experimental Treatment2 Interventions
Mild cognitive impairment due to Alzheimer's disease
Group II: Cohort 2Experimental Treatment2 Interventions
No cognitive impairment, with a family history of Alzheimer's disease
Group III: Cohort 1Experimental Treatment2 Interventions
No cognitive impairment, and no family history of Alzheimer's disease
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Who is running the clinical trial?
University of Wisconsin, MadisonLead Sponsor
1,190 Previous Clinical Trials
3,169,597 Total Patients Enrolled
Sanbrita Mondal, ODPrincipal InvestigatorUniversity of Wisconsin, Madison
Kathleen Schildroth, MDPrincipal InvestigatorUniversity of Wisconsin, Madison
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