- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06508268
Language, Speech and Motor Function in MCI Due to AD and Alzheimer's Disease
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
Status
Conditions
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Marlies Oegema, Master
- Phone Number: 0031+0505953730
- Email: m.oegema@pl.hanze.nl
Study Locations
-
-
-
Groningen, Netherlands, 9714CA
- Recruiting
- Hanze University
-
Contact:
- Oegema Marlies, Master
- Phone Number: 0031505953730
- Email: m.oegema@pl.hanze.nl
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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
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:
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:
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:
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:
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
Collaborators
Study record dates
Study Major Dates
Study Start (Estimated)
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
- NL79836.042.23
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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