Prediction of Amyloid and Mild Cognitive Impairment in Early Stage Alzheimer's Disease From Remote Speech Phenotyping

NCT ID: NCT04928690

Last Updated: 2021-06-16

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 140 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2021-06-20
• Study Completion Date: 2022-08-30

Brief Summary

The S22 study investigates, in a cross-sectional study, the ability of algorithms that analyse acoustic and linguistic patterns of spoken language to predict the presence of amyloid positivity in early stage Alzheimer's disease, specifically in Mild Cognitive Impairment (MCI) and cognitively normal (CN) cohorts; and whether similar algorithms can predict cognitive functioning, in classifying MCI vs CN.

Conditions

Alzheimer Disease; Alzheimer's Disease (Incl Subtypes); Mild Cognitive Impairment

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: CROSS_SECTIONAL

Study Groups

Arm 1: MCI amyloid positive

• Meet the National Institute of Aging - Alzheimer's Association (NIA-AA) core clinical criteria (2011) for MCI due to Alzheimer's
• Positive amyloid PET or amyloid CSF status.
• MMSE 23-30 (inclusive)

No interventions assigned to this group

Arm 2: MCI amyloid negative

• Non-AD Mild Cognitive Impairment (MCI)
• Negative amyloid PET or amyloid CSF status.
• MMSE 23-30 (inclusive)

No interventions assigned to this group

Arm 3: CN amyloid positive

• Absence of a diagnosis of cognitive disorder and/or subjectively reported cognitive decline
• Positive amyloid PET or amyloid CSF status.
• MMSE 26-30 (inclusive)

No interventions assigned to this group

Arm 4: CN amyloid negative

• Absence of a diagnosis of cognitive disorder and/or subjectively reported cognitive decline
• Negative amyloid PET or amyloid CSF status.
• MMSE 26-30 (inclusive)

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Amyloid status must be known, based on an amyloid PET scan or CSF amyloid test, no older than 30 months at the time of consent for Arm 2 and Arm 4 participants (amyloid negative Arms).
• Amyloid status must be known, based on an amyloid PET scan or CSF amyloid test, no older than 60 months at the time of consent for Arm 1 and Arm 3 (amyloid positive Arms).
• Subjects must be aged 50-85 (inclusive).
• Subjects must have MMSE scores of 23-30 (inclusive) based on a test not older than 1 month at the time of the visit.
• Date of diagnosis (if applicable) maximum of five years prior to consent.
• Subjects' first language must be English.
• Willing to participate in a study investigating speech and cognitive impairment.
• Able to provide valid informed consent.
• Able to use, or has a caregiver who is able to use a smartphone device.
• Has access to a smartphone device running an operation system of Android 6 or above; or iOS 10 or above.

• Able to use, or has a caregiver who is able to use a personal computer, notebook or tablet.
• Has access to a personal computing device of that is running an operating system of macOS X with macOS 10.9 or later, or Windows 7 or above, or Ubuntu 12.04 or higher; OR has access internet browser software Internet Explorer version 11 or above; or Microsoft Edge version 12 or above, or Firefox version 27 or above, or Google Chrome version 30 or above, or Safari version 7 or above; AND capable of audio and video recording; AND able to connect to the internet.

Exclusion Criteria

• Clinically significant unstable psychiatric illness in 6 months.
• Diagnosis of General Anxiety Disorder.
• Current, or history within the past 2 years of major depressive disorder diagnosis (according to DSM-5 criteria83); or psychiatric symptoms that, in the opinion of the investigator, could interfere with study procedures.
• History or presence of stroke within the past 2 years.
• Documented history of transient ischemic attack or unexplained loss of consciousness within the last 12 months.
• The participant is using drugs to treat symptoms related to AD, and the doses of these drugs were not stable for at least 8 weeks prior to consent.
• Participant is, or previously has been enrolled in the Sponsor's NOV-0100 or NOV-0110 studies.

• Minimum Eligible Age: 50 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Novoic Limited

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Emil Fristed, MSc

Role: PRINCIPAL_INVESTIGATOR

Novoic Ltd

Central Contacts

Head of Clinical Operations

Role: CONTACT

marton@novoic.com

07849522891

Other Identifiers

NOV-0120

Identifier Type: -

Identifier Source: org_study_id