- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05754086
A Multidimensional Study on Articulation Deficits in Parkinsons Disease
A Multidimensional Study on Articulation Deficits in Parkinson's Disease
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Dysarthria is a motor speech disorder that affects individuals with various etiologies. Parkinson's disease (PD) alone affects nearly one million individuals in the U.S., with dysarthria developing in approximately 90% of these individuals within the first two years of onset. The dysarthria associated with PD is characterized by reduced movement, which has been supported by findings of reduced lip, tongue, and jaw movement in speakers with PD. However, it remains unclear if hypokinetic dysarthria causes a global reduction across all articulators, or if specific articulators are disproportionally affected by the disease. Further, it is not fully understood what factors contribute to speech intelligibility. Specifically, little is known about the articulatory-kinematic correlates of speech intelligibility. This missing link is vital to understand, as articulation deficits are a universal characteristic of dysarthria, regardless of etiology. The proposed study provides a linked investigation of kinematic, acoustic, and perceptual characteristics in speakers with PD and neurologically healthy speakers.
This research aims to (1) examine the perceptual, acoustic, and articulator-specific movement deficits in speakers with PD and (2) understand the relationship between articulatory movement and measures of speech perception. Specific Aim 1 will examine the group differences between speakers with PD and neurologically healthy speakers using perceptual, acoustic, and articulator-specific kinematic measures. The investigators hypothesize the perceptual, acoustic, and tongue-related kinematic measures will differentiate individuals with PD from neurologically healthy speakers. Specific Aim 2 will model speech intelligibility (Specific Aim 2a) and ratings of articulatory precision (Specific Aim 2b) using selected acoustic and kinematic measurements. The investigators hypothesize that the acoustic measures will be stronger predictors of speech intelligibility than the kinematic measures, as they are both derived from the speech signal. Further, the investigators hypothesize the selected kinematic measures may demonstrate a stronger relationship to articulation ratings than speech intelligibility. This study is a requisite step toward our long-term goal of advancing dysarthria management strategies. The primary outcome will be explanatory models that identify acoustic and articulatory correlates of speech intelligibility and articulatory precision. This study has important implications for developing articulator-specific dysarthria management strategies to supplement universal dysarthria management strategies.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Florida
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Tallahassee, Florida, United States, 32309
- Florida State University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- neurological diagnosis of PD (for the PD group only)
- diagnosis of dysarthria (for the PD group only)
- native English speaker
- no evidence of cognitive impairment, as indicated by a score above 26 on the Montreal Cognitive Assessment
- able to read a paragraph in 19-point font
Exclusion Criteria:
- Not within the age limits
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Parkinsons (PD) Group
This cohort includes individuals who have been diagnosed with Parkinson's disease.
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This behavioral modification asks participants to speak more clearly, as if they were "speaking to someone with a hearing loss".
This behavioral modification asks participants to speak less clearly, as if they were "in a room with many people and they were mumbling something to the person next to them that they didn't want other people in the room to hear."
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Neurotypical (NT) Group
This group consists of age-matched control participants.
They are neurologically healthy and do not have any neurological diagnoses.
|
This behavioral modification asks participants to speak more clearly, as if they were "speaking to someone with a hearing loss".
This behavioral modification asks participants to speak less clearly, as if they were "in a room with many people and they were mumbling something to the person next to them that they didn't want other people in the room to hear."
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Vowel Space Area
Time Frame: Baseline
|
Vowel space area is a measure of the planar area among the four corner vowels /i/, /ae/, /a/, and /u/.
It is calculated using the first and second formant resonant frequencies obtained from the acoustic signal, using the software PRAAT.
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Baseline
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Tongue and Jaw Speed
Time Frame: Baseline
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This is measured as the tongue and jaw speed during the diphthong in "Buy".
Specifically, this will be calculated as tongue/jaw movement (measured in mm), divided by movement duration (measured in ms).
The tongue and jaw movement will be collected using the electromagnetic articulography (EMA) device used in this study.
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Baseline
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Acoustic Distance
Time Frame: Baseline
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This is measured as the Euclidean distance between the second formant frequency (F2) onset and offset of the diphthong in "Buy" in an F1-F2 (first and second formant frequency) space.
Measured in Hz.
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Baseline
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Tongue and Jaw Distance
Time Frame: Baseline
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This is measured as the Euclidean distance between the tongue and jaw onset and offset of the diphthong in "Buy" in a two-dimensional space.The tongue and jaw movement will be collected using the electromagnetic articulography (EMA) device used in this study.
|
Baseline
|
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F2 Slope
Time Frame: Baseline
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Second formant frequency (F2) slope is measured as the rate of F2 change during the diphthong in "Buy."
To calculate this measure, first the investigators will obtain the extent of F2 change (max F2 - min F2) from the diphthong "Buy."
Then this F2 change is divided by the duration of the diphthong "Buy."
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Baseline
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Yunjung Kim, Ph.D., Florida State University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Neurologic Manifestations
- Neurobehavioral Manifestations
- Parkinsonian Disorders
- Basal Ganglia Diseases
- Movement Disorders
- Synucleinopathies
- Neurodegenerative Diseases
- Language Disorders
- Communication Disorders
- Speech Disorders
- Articulation Disorders
- Parkinson Disease
- Dysarthria
Other Study ID Numbers
- STUDY00002525
- F31DC020121 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- ANALYTIC_CODE
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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