Language, Speech and Motor Function in MCI Due to AD and Alzheimer's Disease

July 17, 2024 updated by: Hans Hobbelen, Hanze University of Applied Sciences Groningen

Language, Speech and Motor Function in Mild Cognitive Impairment Due to AD and Alzheimer's Disease

The goal of this observational cross-sectional study is to explore the characteristics of language, speech, and motor function in persons with Mild Cognitive Impairment due to Alzheimer's disease ("MCI due to AD") and persons with mild and moderate Alzheimer's disease ("AD"). This study aims to:

  • Explore motor, speech, and language functions in MCI due to AD and mild and moderate AD.
  • Combine the characteristics of motor, language, and speech functions to gain more insight into the association of language, speech, and motor changes during MCI due to AD and mild and moderate AD.

Researchers will compare the outcomes to an age-matched control group without cognitive impairment.

Participants will undergo:

  • Two motor function tests to assess gait and hand grip strength.
  • Four language and speech function tests to assess spontaneous speech and verbal fluency..

Study Overview

Study Type

Observational

Enrollment (Estimated)

208

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Groningen, Netherlands, 9714CA
        • Recruiting
        • Hanze University
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

The envisaged total participants of this study is: 52 persons with MCI due to AD, 52 persons with mild AD, 52 persons with moderate AD, 52 and 52 age-matched persons without cognitive impairment. The first language of the participants is either Frisian and/or Dutch. The participants may in addition to that also speak a Dutch dialect or another language

Description

Inclusion Criteria:

A subject with MCI with a likelihood of underlying AD pathophysiology must meet the following criteria:

  • Established diagnosis of MCI due to AD with a likelihood according to NIA-AA criteria (Albert et al., 2011).
  • A score of stage three on the Global Deterioration Scale (GDS) (Reisberg et al., 1982).

A subject with AD must meet the following criteria:

  • Established diagnosis of AD (amnestic or non-amnestic) or etiologically mixed presentation of AD according to DSM-5 (American Psychiatric Association, 2013) or NINCDS-ARDRA criteria (Jack et al., 2018; McKann et al., 2011).
  • The following scores on the Global Deterioration Scale (GDS): four for mild AD, five for moderate AD (Reisberg et al., 1982).

All subjects of the control group must meet the following criteria:

  • A score of stage one or two on the Global Deterioration Scale (GDS) (Reisberg et al., 1982).
  • They are age-matched with the MCI due to AD or AD patients included in the study.

All subjects must meet the following criteria:

  • First language is Dutch and/or Frisian.
  • Able to walk independently with or without walking aid.
  • Able to squeeze with each hand.

Exclusion Criteria:

A subject with MCI due to AD or AD who meets the following criteria will be excluded from participation in this study:

  • Having a neurological or neurodegenerative disease or disorder that may be contributing to cognitive impairment above and beyond that caused by AD or mixed AD; Down's syndrome, other subtypes of dementia, autism spectrum disorder.
  • Having an established diagnosis of a psychiatric disorder, e.g. schizophrenia, depression.

All subjects in the control group who meets following criteria will be excluded from participation in this study:

● Suffers from a neurological, neurodegenerative or psychiatric disease or disorder.

All subjects in any group who meet any of the following criteria will be excluded from participation in this study:

  • Hearing loss (with or without hearing aid) that affects communication.
  • Vision loss (with or without glasses or lenses) that affects communication.
  • History of language problems, speech problems or dyslexia.
  • Suffers from additional disorders or diseases which may limit gait, hand grip strength, language and/or speech.
  • Medication use that influence gait, hand grip strength, speech or language performance at time of testing.
  • Being terminally ill (i.e., life expectancy < 2 weeks according to the attending physician).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Persons with Mild Cognitive Impairment due to AD
Gait will be assessed by the GAITRite walkway system OR the 4-meter walking speed test
Hand grip strength will be assessed by a Jamar hand dynamometer
Characteristics Dutch/Frisian language Language and speech will be assessed by the Cookie Theft Picture-task (a picture description task from Berube et al., 2019)
Other Names:
  • Cookie Theft Picture
Characteristics Dutch/Frisian language and speech will be assessed by an autobiographical semi-structured conversation
The mental lexicon of Dutch/Frisian language will be assessed by a two verbal fluency tests, including letter fluency and categorical fluency
Persons with mild AD
Gait will be assessed by the GAITRite walkway system OR the 4-meter walking speed test
Hand grip strength will be assessed by a Jamar hand dynamometer
Characteristics Dutch/Frisian language Language and speech will be assessed by the Cookie Theft Picture-task (a picture description task from Berube et al., 2019)
Other Names:
  • Cookie Theft Picture
Characteristics Dutch/Frisian language and speech will be assessed by an autobiographical semi-structured conversation
The mental lexicon of Dutch/Frisian language will be assessed by a two verbal fluency tests, including letter fluency and categorical fluency
Persons with moderate AD
Gait will be assessed by the GAITRite walkway system OR the 4-meter walking speed test
Hand grip strength will be assessed by a Jamar hand dynamometer
Characteristics Dutch/Frisian language Language and speech will be assessed by the Cookie Theft Picture-task (a picture description task from Berube et al., 2019)
Other Names:
  • Cookie Theft Picture
Characteristics Dutch/Frisian language and speech will be assessed by an autobiographical semi-structured conversation
The mental lexicon of Dutch/Frisian language will be assessed by a two verbal fluency tests, including letter fluency and categorical fluency
Persons without cognitive impairment, age-matched with persons with MCI due to AD and AD
Gait will be assessed by the GAITRite walkway system OR the 4-meter walking speed test
Hand grip strength will be assessed by a Jamar hand dynamometer
Characteristics Dutch/Frisian language Language and speech will be assessed by the Cookie Theft Picture-task (a picture description task from Berube et al., 2019)
Other Names:
  • Cookie Theft Picture
Characteristics Dutch/Frisian language and speech will be assessed by an autobiographical semi-structured conversation
The mental lexicon of Dutch/Frisian language will be assessed by a two verbal fluency tests, including letter fluency and categorical fluency

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Language and speech characteristics of spontaneous speech
Time Frame: 4 months
Autobiographical semi-structured interview and a picture description task ("The Cookie Theft Picture (Berube et al., 2019))
4 months
Verbal fluency
Time Frame: 4 months
Naming animals and professions
4 months
Letter fluency
Time Frame: 4 months
Naming letters starting with the letters D and A
4 months
Temporal and spatial parameters of gait
Time Frame: 4 months
Gaitrite walkway system (GAITRite) or 4-meter walking speed test
4 months
Hand grip strength
Time Frame: 4 months
Jamar hand dynamometer
4 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

July 12, 2024

Primary Completion (Estimated)

February 9, 2025

Study Completion (Estimated)

February 9, 2025

Study Registration Dates

First Submitted

May 22, 2024

First Submitted That Met QC Criteria

July 17, 2024

First Posted (Actual)

July 18, 2024

Study Record Updates

Last Update Posted (Actual)

July 18, 2024

Last Update Submitted That Met QC Criteria

July 17, 2024

Last Verified

July 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

This study is based on FAIR principles (Findable, Accessible, Interoperable and Reusable). This means that, all anonymized data and meta-data will be archived and shared during or after 5 years after completion of this study in one or more of the following database systems: Faith Research (https://www.faithresearch.nl/), DANS ('Data Archiving and Networked Services) and DataverseNL (https://dataverse.nl).

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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