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RecruitingNCT06578416Updated Nov 10, 2026

The Development of Stuttering in Young Children

An observational study in Stuttering, Stuttering, Childhood and Stuttering, Developmental, sponsored by Michigan State University. Recruiting at 1 site in United States. Open to participants aged 3 Years to 6 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-10.

Sponsored by Michigan State University · Observational

From the registry’s dates

  • Started Jun 2023; still recruiting 3 years 5 months later.
Study type
Observational
Model
Case-control
Time perspective
Other
Enrollment
120
Ages
3 Years to 6 Years
Sex
All
01

Study summary

The goal of this longitudinal research is to learn why some children "grow out" of stuttering, while others persist. Children who do and do not stutter aged 3-6 years are eligible to participate in our study. During the study, children's speech and language abilities will be assessed with standardized assessments, and they complete several child-friendly experiments. During these experiments, brain activity will be recorded using specialized caps while children describe pictures, children will speak in two virtual-reality scenarios, and produce speech while keeping to a beat.

Read the detailed description

The length of participation in our study depends on the subset of activities completed. Families in the longitudinal study will take part in three visits each lasting approximately 2 hrs for up to 5 years.

Parents and caregivers will complete parent questionnaires (1 x each year for up to 5 years) and a 5-minute, online survey in between visits to the lab (1x each year for up to 5 years). Children will take part in standardized and observational assessments (1x each year for up to 5 years). These may cover aspects of social/emotional development, cognition, and speech, language, and hearing abilities. These tests are used to assess whether a child falls within or outside of the normative range for his/her age.

Children will participate in one or more of the following tasks (1x each year for up to 5 years)

  • Listen to sounds or words and view or name pictures presented on a monitor. Brain activity electroencephalography (EEG) will be recorded while children listen to speech sounds and name pictures. This will be done with an elastic cap that holds special sensors (electrodes). Sensors will also be placed behind each ear, beside each eye, and under the left eye.
  • Virtual reality (VR). Children wear a VR headset and experience virtual, age-appropriate talking situations (e.g., answering questions in a classroom). While they talk in these scenarios, the headset measures where they are looking (eye tracking), and sensors on their forehead, hand, and finger measure their heart rate and sweat response.
  • Children will watch cartoons of animals jumping to a consistent beat (rhythm) and produce a word in time with the animal jumping/beat.
  • Children will repeat nonwords, name pictures, or count while wearing a cap with sensors. Half of the sensors emit light through while the other half measures the reflected light. These sensors give us information about brain activity and are not harmful.
02

Conditions studied

  • Stuttering
  • Stuttering, Childhood
  • Stuttering, Developmental

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03

In context

Stuttering

74 studies on the registry are indexed under Stuttering; 23 are open to participants now.

This study's planned enrollment of 120 is above the median of 60 across 15 observational studies indexed under Stuttering.

Browse Stuttering studies →

Lead sponsor

Michigan State University is the lead sponsor of 143 studies on the registry; 27 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
3 Years to 6 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Preschool children who do and do not stutter

Eligibility criteria

Inclusion Criteria for controls:

  • English as first/primary language
  • No history of neurological disease
  • Normal or corrected visual acuity
  • No medications expected to affect performance
  • No intellectual impairment, autism spectrum disorder, ADHD
  • Age-appropriate scores on speech and language assessment battery
  • Pass hearing screening at 20 dB at 500, 1000, 2000, and 4000, bilaterally

Inclusion Criteria for children who stutter:

  • English as first/primary language
  • No history of neurological disease
  • Normal or corrected visual acuity
  • No medications expected to affect performance
  • No intellectual impairment or ASD Scores on speech and language assessments indicating stuttering, phonological (speech sound), or language disorders
  • Pass hearing screening at 20 dB at 500, 1000, 2000, and 4000, bilaterally
05

Study design

Observational model
Case-control
Time perspective
Other
Enrollment
120 participants (estimated)
Patient registry
No

Groups and cohorts

  • Children who stutter

    Preschool children who stutter aged 3 to 6-years

    Diagnostic Test: Standardized assessments of speech and language abilities

  • Children who do not stutter

    Preschool children who do not stutter aged 4 to 6-years

    Diagnostic Test: Standardized assessments of speech and language abilities

Interventions

  • Diagnostic testStandardized assessments of speech and language abilities

    Standardized and observational assessment of speech and language abilities

06

What researchers measure

Primary outcomes

  1. Stuttering Severity

    Assess speech for the presence of stuttering disfluencies and calculate the severity of stuttering based on parent ratings and calculated as the percentage of disfluent syllables out of the total syllables of speech produced.

    Time frame: 1 x each year for up to 5 years

  2. Virtual reality speaking scenarios

    Record looking events in msec during virtual reality scenarios (classroom of children and kitten)

    Time frame: 1 x each year for up to 5 years

  3. Virtual reality speaking scenarios

    Pulse oximetry measures will be taken with a photoplethysmograph transducer (Biopac TSD200) secured around the distal phalanx of the fourth finger of the child's non-dominant hand with a Velcro strap. Two measures will be analyzed. (1) Blood pulse volume (BPV) amplitude, the average trough-to-peak amplitude (in volts) of pulse cycles across segments where the child is producing speech and (2) Pulse rate (PR in pulses per minute ppm), will be recorded for each speech segment then averaged. These pulse oximetry measures will be taken during the viewing of virtual reality scenarios (classroom of children and kitten)

    Time frame: 1 x each year for up to 5 years

  4. Virtual reality speaking scenarios

    Electrodermal (skin conductance) recordings will be collected from the hands while children are immersed in virtual reality speaking scenarios (classroom of children and kitten). We report skin conductance levels and skin conductance response frequency and amplitude in microSiemens (mS).

    Time frame: 1 x each year for up to 5 years

  5. EEG recording of event-related brain potentials

    Electroencephalographic (EEG) recordings of event-related brain potentials will be conducted during a picture identification task. ERPs will be averaged across conditions and reported in microvolts.

    Time frame: 1 x each year for up to 5 years

  6. Speech production synchronization

    We record productions of a word spoken to the beat under different feedback conditions. We will assess timing measures reflecting the accuracy with which children synchronize their speech to the beat and retain the rhythm.

    Time frame: 1 x each year for up to 5 years

  7. fNIRS recording of cortical hemodynamic responses

    Cerebral hemodynamic responses are recorded during the experiment with a continuous-wave fNIRS system (NIRx, Inc). The system uses LED light source optodes, and avalanche photodiode optode detectors for measuring intensity changes in the diffused light at a 10-Hz sampling rate. The optodes are embedded in a standard EEG cap. The concentrations of oxygenated hemoglobin and deoxygenated hemoglobin in micromols will be calculated across trial intervals as participants describe child-friendly picture scenes. These responses will then be averaged across trials for each child.

    Time frame: 1 x each year for up to 5 years

07

Study locations

1 of 1 sites recruiting
  • Developmental Speech Lab
    East Lansing, Michigan 48824, United States
    Recruiting
08

Updates

1 registry update since Sep 25, 2026
Minor edits
Nothing that changes what the study is or who can join. Edited: verification date
1 update, last Nov 10, 2026
Show all 1 update
  1. Nov 10, 2026
    Minor edits only
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT06578416
Responsible party
Bridget Walsh (Associate Professor of Communicative Sciences and Disorders, Michigan State University) — Principal investigator
First posted
Aug 29, 2024
Start date
Jun 1, 2023
Primary completion
Jun 2027 (estimated)
Completion
Jun 2027 (estimated)
Last update
Nov 10, 2026

Study contacts

Katelyn Gerwin, Ph.D.
Contact
msustutteringlab@gmail.com
5173553410
Bridget Walsh, Ph.D.
Contact
msustutteringlab@gmail.com
5173553410

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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