Validation of a Digital Self-Administered Cognitive Screening Tool: MoCA-XpressO

Sponsor
MoCA Clinic and Institute (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05879562
Collaborator
(none)
100
1
2
8.9
11.2

Study Details

Study Description

Brief Summary

The investigators conducted a validation study for the Montreal Cognitive Assessment (MoCA)-XpressO compared to the digital-MoCA test (version 8.1) as the gold standard. Participants were recruited from the MoCA clinic and a family practice. Ethics approval was received, and all participants provided informed consent. A crossover study design was applied to the MoCA-XpressO and the digital-MoCA test; participants were randomized for the order of administration. The investigators only recruited participants who did not complete a MoCA test during the 3 months prior to the study. A logistic regression model was built, and the accuracy of the model was evaluated by the sensitivity, specificity, and area under the Receiver Operating Characteristic (ROC) curve.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: MoCA-Xpresso
N/A

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 Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Participant)
Masking Description:
Participants are blinded to which test is the one being validated.
Primary Purpose:
Screening
Official Title:
Montreal Cognitive Assessment (MoCA) XpressO: Validation of a Digital Self-administered Cognitive Pre-screening Tool for the General Adult Population
Actual Study Start Date :
Oct 1, 2022
Anticipated Primary Completion Date :
Jun 30, 2023
Anticipated Study Completion Date :
Jun 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: MoCA-Xpresso first

Participants in the study will complete the MoCA-Xpresso test before the digital-MoCA classic test.

Diagnostic Test: MoCA-Xpresso
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.

Diagnostic Test: MoCA-Xpresso
MoCA-Xpresso is a home-based, self-administered digital cognitive screening tool, based on a tablet device.

Outcome Measures

Primary Outcome Measures

  1. Correlation between the MoCA XpressO and the Digital MoCA [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

Secondary Outcome Measures

  1. Correlation between scores of sub-tests on MoCA-XpressO and the Digital MoCA [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

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 MoCA Clinic and Institute Greenfield Park Quebec Canada J4V 2J2

Sponsors and Collaborators

  • MoCA Clinic and Institute

Investigators

  • Principal Investigator: Ziad Nasreddine, MD, MoCA Clinic and Institute, 4896 Taschereau Blvd bureau 230, Greenfield Park, Quebec J4V 2J2

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
MoCA Clinic and Institute
ClinicalTrials.gov Identifier:
NCT05879562
Other Study ID Numbers:
  • MoCA Xpresso 01
First Posted:
May 30, 2023
Last Update Posted:
May 30, 2023
Last Verified:
May 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by MoCA Clinic and Institute
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 30, 2023