Prediction of Visual Feedback Effects on Speech Motor Adaptation in Healthy Adults
PVF
2 other identifiers
interventional
40
1 country
1
Brief Summary
This study examines whether individual differences in how speakers respond to hearing versus physical sensation during speech can predict who benefits most from visual feedback during a speech task. Healthy adults will complete a series of tasks in which auditory feedback is altered in real time through headphones, with and without an added visual display of the speech signal. A computational model will be used to estimate how strongly each participant relies on hearing versus physical sensation when monitoring speech. The study will then test whether this individual profile predicts how much the visual display improves each participant's ability to respond to the altered feedback.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable healthy-volunteers
Started Apr 2026
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
April 2, 2026
CompletedFirst Posted
Study publicly available on registry
April 15, 2026
CompletedStudy Start
First participant enrolled
April 20, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
August 15, 2026
Study Completion
Last participant's last visit for all outcomes
November 30, 2026
April 15, 2026
April 1, 2026
4 months
April 2, 2026
April 8, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Mean difference in F1 compensation magnitude between auditory-visual and auditory-only feedback conditions of standard adaptive feedback task
Visual gain is defined as the within-participant difference in acoustic compensation magnitude (measured from formant frequencies) between the auditory-visual feedback condition and the auditory-only condition of the standard adaptive feedback task. Greater visual gain indicates a larger compensatory response when visual feedback is available.
During study visit (Day 1)
Study Arms (1)
Altered Auditory Feedback With and Without Visual Feedback
EXPERIMENTALAll participants complete altered auditory feedback tasks without visual feedback (baseline phase) followed by the same task with simultaneous real-time visual-acoustic biofeedback. Both conditions are administered within a single study visit.
Interventions
Participants produce speech while hearing real-time altered auditory feedback delivered through headphones. Two task variants are administered: a fast-adapt design in which the altered feedback is introduced and withdrawn repeatedly, and a standard adaptive design in which the altered feedback is introduced once and maintained for an extended run. Administered to all participants as the baseline condition.
Participants perform the standard adaptive auditory feedback task with the addition of real-time visual display. The visual display presents the altered auditory signal alongside a visual target derived from the participant's baseline production. Administered to all participants following the auditory-only baseline phase.
Eligibility Criteria
You may qualify if:
- Age 18 to 45 years
- Self-reported English as dominant or equally dominant language (learned English by age 3)
- No self-reported history of significant speech, language, or hearing difficulty
- Pass pure-tone hearing screening at 25 dB HL
- Pass qualitative screening of speech, voice, and resonance based on connected speech sample
You may not qualify if:
- Learned English after age 3
- English is not a dominant language
- History of speech or language disorder, hearing loss, or neurodevelopmental disorder (e.g., autism spectrum disorder, Down syndrome)
- Failure to pass pure-tone hearing screening
- Failure to pass qualitative screening of speech, voice, and resonance
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
New York University
New York, New York, 10012, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Tara McAllister, PhD
New York University
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
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
April 2, 2026
First Posted
April 15, 2026
Study Start (Estimated)
April 20, 2026
Primary Completion (Estimated)
August 15, 2026
Study Completion (Estimated)
November 30, 2026
Last Updated
April 15, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- ANALYTIC CODE
- Time Frame
- Data will be shared within 1 year of the study end date and will be made available indefinitely.
- Access Criteria
- Publicly accessible
Complete de-identified data and scripts to reproduce analyses reported in study manuscripts