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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05881239
Other study ID # 2022P002451
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 9, 2023
Est. completion date May 2025

Study information

Verified date March 2024
Source Massachusetts General Hospital
Contact Mark W Albers, MD PhD
Phone 617-724-7401
Email albers.mark@mgh.harvard.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this study is to objectively test one's sense of smell, called olfaction, in participants with Subjective Cognitive Concerns (SCC), Mild Cognitive Impairment, Mild Behavioral Impairment (MBI), and age-matched controls. The main question it aims to answer is whether the AROMHA Brain Health Test could serve as a predictive biomarker of neurodegenerative disorders. This understanding will aid in the development of a noninvasive, cost-effective diagnostic tool that reliably and specifically distinguishes disease and normal aging populations. Participants will take the approximately 45-minute AROMHA Brain Health Smell Test where they will peel and sniff labels on the physical smell cards and answer questions on the web-based app relating to what they smelled. Participants will undergo tests for odor intensity, odor identification, odor discrimination, and episodic olfactory memory, but will not be provided the results of these tests.


Recruitment information / eligibility

Status Recruiting
Enrollment 250
Est. completion date May 2025
Est. primary completion date December 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - A clinical or research consensus diagnosis of the patient's condition or control status. - Individuals that are at least 18 years of age at the time of enrollment. - Individuals that are no older than 100 years of age at the time of enrollment. Exclusion Criteria: - Primary pulmonary disease such as severe emphysema or asthma not under good medical control. - Current sinusitis, common cold, upper respiratory infection, or nasal polyps. - Current or recent (past 6 months) alcohol or substance dependence. A prior history of alcohol or substance abuse will not be grounds for exclusion. - Pregnancy. - Severe cognitive dysfunction that would preclude completion of the olfactory testing. - An adverse reaction to fragrances (ie. they trigger a severe asthmatic attack or nausea).

Study Design


Intervention

Device:
AROMHA Brain Health Test
The AROMHA Brain Health Test is a self-administered, at-home smell test developed as a potential primary screen for identifying individuals at risk for developing Alzheimer's and as a means to follow disease progression in individuals without overt cognitive symptoms. The smell test device consists of five physical smell cards and a paired web-based app that directs participants on how to sample odors and asks them questions regarding what they have smelled. The 45-minute smell test battery includes measures of odor intensity, identification, memory, and discrimination.

Locations

Country Name City State
United States Massachusetts General Hospital Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary AROMHA Brain Health Test The AROMHA Brain Health Test is a battery of 18 odors across 5 smell cards. The subject smells each odor label and is tested on odor intensity, identification, memory, and discrimination. An increased number of correct responses indicates a better sense of smell. We will evaluate MCI patients' performance against age-matched controls. 1 hour
Secondary AROMHA Brain Health Test The AROMHA Brain Health Test is a battery of 18 odors across 5 smell cards. The subject smells each odor label and is tested on odor intensity, identification, memory, and discrimination. An increased number of correct responses indicates a better sense of smell. We will evaluate MBI patients' performance against age-matched controls. 1 hour
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