Vowel Space Expansion Sensorimotor Adaptation
Behavioral and Neural Measures of Speech Motor Control
4 other identifiers
interventional
117
1 country
1
Brief Summary
The purpose of this research study is to understand how the brain processes and controls speech in healthy people. The investigators are doing this research because it will help identify the mechanisms that allow people to perceive their own speech errors and to learn new speech sounds. 117 participants will be enrolled into this part of the study and can expect to be on study between 1 day (Experiment 1) and 4 weeks (Experiment 2).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Feb 2024
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 22, 2024
CompletedFirst Posted
Study publicly available on registry
January 31, 2024
CompletedStudy Start
First participant enrolled
February 15, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 1, 2026
April 9, 2026
August 1, 2025
2.3 years
January 22, 2024
April 8, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Average Vowel Spacing (AVS) Measured as the Mean of Pairwise Formant Distances Between Vowels
AVS is a local measure of vowel spacing.
up to 1 hour (Exp 1,3); eight visits of 1 hour each over 4 weeks (Exp 2)
Quadrilateral Vowel Space Area (qVSA)
qVSA measures the area (in Hz\^2) between the F1/F2 coordinates of the corner vowels. This is a global measure of working vowel space.
up to 1 hour (Exp 1,3); eight visits of 1 hour each over 4 weeks (Exp 2)
Intelligibility measured by Percent of words correctly identified by 5 independent transcribers
Intelligibility is a perceptual measure. Four repetitions of each spoken production from each adaptation phase, as well as the minimal-pair neighbors from the calibration phase, will be identified by all transcribers. Because intelligibility in healthy speakers is expected to be near ceiling, speech signals will be masked by speech-shaped noise and delivered at 72 dB over closed-ear headphones. Signal-to-noise ratio will be determined prior to testing as the ratio where, on average, 50% of stimuli in the calibration phase are correctly identified. Transcribers will be native English speakers with no history of neurological/hearing disorders who pass a pure-tone hearing test.
up to 1 hour (Exp 1,3); eight visits of 1 hour each over 4 weeks (Exp 2)
Auditory acuity is measured as the average just noticeable difference (JND) along 4 vowel formant continua
Auditory acuity is measured as the average just noticeable difference (JND) along 4 vowel formant continua: /i/-/ɪ/, /ɛ/-/æ/, /u/-/ʊ/, and /ɑ/-/ʌ/. Acuity will be measured at continua midpoint (across-category acuity) and at the four corner vowel endpoints (within-category acuity). JNDs will be measured through a 4-interval, 2-alternative forced choice task (AABA or ABAA) via a staircase procedure.
up to 1 hour (Exp 1,3); eight visits of 1 hour each over 4 weeks (Exp 2)
Study Arms (1)
Healthy Adult Speakers
EXPERIMENTALhealthy adult participants across the lifespan in three groups:18-35, 36-55, and 56+
Interventions
Participant will sit in front of a computer screen in a quiet room and to produce speech based on what is on the screen. Participant may see real words or nonsense words to read. Investigators may play sounds through headphones and ask the participant to repeat them. Participant speech will be recorded by a microphone. This task takes about one hour to complete.
Eligibility Criteria
You may qualify if:
- English-speaking adults
- normal hearing and speech
- no history of stroke or neurological conditions
You may not qualify if:
- Native language other than English
- Any neurological disorders other than the disorder of interest
- Any history of hearing disorders
- Uncorrected vision problems that prevent participants from seeing visually-presented stimuli
- Significant cognitive impairments that prevent participants from carrying out the task or from giving informed consent
- Vulnerable populations (minors and prisoners)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Wisconsin
Madison, Wisconsin, 53705, United States
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Carrie Niziolek, PhD
University of Wisconsin, Madison
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 22, 2024
First Posted
January 31, 2024
Study Start
February 15, 2024
Primary Completion (Estimated)
June 1, 2026
Study Completion (Estimated)
June 1, 2026
Last Updated
April 9, 2026
Record last verified: 2025-08
Data Sharing
- IPD Sharing
- Will share