- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05879562
Validation of a Digital Self-Administered Cognitive Screening Tool: MoCA-XpressO (MoCA)
Montreal Cognitive Assessment (MoCA) XpressO: Validation of a Digital Self-administered Cognitive Pre-screening Tool for the General Adult Population
Study Overview
Status
Intervention / Treatment
Detailed Description
Introduction:
The MoCA XpressO is a self-administered medical digital cognitive screening test. This test can help individuals assess whether they should have concerns regarding their cognition and should bring these concerns up to their physician. The test can be administered in an empty office in the clinic, or in the comfort of the patient's home.
The MoCA Classic test was first published in 2005 by Nasreddine et al. (The Montreal Cognitive Assessment, MoCA: A Brief Screening Tool for Mild Cognitive Impairment. J Am Geriatr Soc, 2005, 53:695-9.) The MoCA Classic test (version 8.2) is a one-page 30-point test administered in 10 minutes. The test and administration instructions are freely accessible at www.mocatest.org. The test is available in over 55 languages and dialects. The MoCA Classic assesses several cognitive domains. The short-term memory recall task (5 points) involves two learning trials of five nouns and delayed recall after approximately 5 minutes. Visuospatial abilities are assessed using a clock-drawing task (3 points) and a three-dimensional cube copy (1 point). Multiple aspects of executive functions are assessed using an alternation task adapted from the trail-making B task (1 point), a phonemic fluency task (1 point), and a two-item verbal abstraction task (2 points). Attention, concentration and working memory are evaluated using a target detection task (1 point), a serial subtraction task (3 points), and a forward and backward digit sequence task (1 point each). Language is assessed using a three-item confrontation naming task with low- familiarity animals (3 points), a two-item syntactically complex sentence repetition task (2 points), and the aforementioned fluency task. Finally, orientation to time and place is evaluated (6 points).
Study objectives/purpose:
This study seeks to validate the MoCA XpressO self-administered digital test compared to the MoCA Classic test for adults aged 50+. The study's goal is to confirm its performance as a viable screening tool to flag concerns regarding cognition in this population.
Objectives and Hypotheses:
Primary Objective: establish validity by comparing the MoCA XpressO vs. the digital MoCA Classic test.
Validity Outcome 1: Correlation between the total score of MoCA XpressO and the total score of the digital MoCA Classic test.
Hypothesis 1: There will be a significant correlation between the total scores of the MoCA XpressO and MoCA Classic test.
Secondary Objective: explore the users' experience of the MoCA XpressO test through subjective feedback from the participant.
Outcome 2: subjective feedback about user experience for participant (Likert Scale) Hypothesis 2: user experience will be rated high (>=4) on a Likert scale 1-5.
Additional exploratory measures/data:
Demographic information (age, level of education etc.); diagnosis; previous MMSE or MoCA score if available; frequency of technological use
Study Sample: the target number of participants is 100. Participants will be recruited from the MoCA Memory Clinic and Institute and the Cornwall family practice clinic. Participants in this study will consist of adults age 50 and over, with no restrictions to sex, gender, or ethnicity. There will be an equal number of participants with normal cognition, mild cognitive impairment, and mild AD. They must speak English or French and have at least 6 years of formal schooling.
Study locations: 2 clinical sites will recruit potentially eligible participants. (1) MoCA Clinic and Institute, Greenfield Park, Québec, Canada; and (2) Family Medicine Practice, Cornwall, Ontario, Canada
Randomization:
The order of administration of the MoCA XpressO and the digital MoCA Classic test will be determined randomly so that each test will have similar chances of being first, or second. The same rater will be performing the MoCA Classic test in each clinic participating in the validation study.
Blinding: The participants are blinded to the screening test that is being studied. The researcher doing the analysis will be blinded to the order of randomization.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Quebec
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Greenfield Park, Quebec, Canada, J4V 2J2
- MoCA Clinic and Institute
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age 50 years and over
- All gender inclusive
- All sex inclusive
- Fluent in English or in French
- Minimum 6 years of formal education
- Minimum total score of 11/30 on MoCA test
Exclusion Criteria:
- Age younger than 50 years
- Less than 6 years of formal schooling
- Total score on MoCA test less than 11/30
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: MoCA-Xpresso first
Participants in the study will complete the MoCA-Xpresso test before the digital-MoCA classic test.
|
MoCA-Xpresso is a home-based, self-administered digital cognitive screening tool, based on a tablet device.
|
|
Experimental: MoCA-Xpresso second
Participants in the study will complete the digital-MoCA classic test before the MoCA-Xpresso test.
|
MoCA-Xpresso is a home-based, self-administered digital cognitive screening tool, based on a tablet device.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Correlation between the MoCA XpressO and the Digital MoCA
Time Frame: up to 30 minutes (for completion of all intervention included in the study)
|
Correlation between the total score of MoCA XpressO and the total score of the Digital MoCA Classic
|
up to 30 minutes (for completion of all intervention included in the study)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Correlation between scores of sub-tests on MoCA-XpressO and the Digital MoCA
Time Frame: up to 30 minutes (for completion of all interventions in the study)
|
Correlation between the scores of the sub-tests on MoCA XpressO and the scores of the sub-tests on the Digital MoCA Classic
|
up to 30 minutes (for completion of all interventions in the study)
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ziad Nasreddine, MD, MoCA Clinic and Institute, 4896 Taschereau Blvd bureau 230, Greenfield Park, Quebec J4V 2J2
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MoCA Xpresso 01
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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