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Stuttering, ChildhoodNCT05286151

Network Connectivity and Temporal Processing in Adolescents Who Stutter

A study testing Rhythm discrimination in people with Stuttering, Childhood and Stuttering, run by University of Michigan at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

The specific purpose of this clinical trial is to compare performance on rhythm perception and production tasks between children who stutter and children who do not stutter. The overall project also aims to investigate how performance on rhythm tasks may be related to brain activity (non-clinical trial). Read more about this study

Who is it for?
Ages 9 to 13 yearsHealthy volunteers can take part
Conditions the study is for
Stuttering, Childhood, Stuttering
What is being tested?
Rhythm discrimination
Could I receive a placebo?
No, everyone receives an active treatment
How many people
500 participants
Where
1 siteUnited States
Study dates
23 Jul 2022to 31 Jan 2028
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 9 to 13 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • English as primary language
  • Current or past stuttering diagnosis
  • English as primary language

Who cannot join

  • Diagnosed/under treatment for any neurological or psychiatric conditions
  • Head trauma with loss of consciousness
  • Major medical illness
  • Hearing loss- Language/motor delay (below -2 standard deviations on standardized assessments)
  • Face, motor, or reflex abnormalities
  • Personal or family history of stuttering
Show all 12Show fewer
  • Diagnosed/under treatment for any neurological or psychiatric conditions
  • Head trauma with loss of consciousness
  • Major medical illness
  • Hearing loss
  • Language/motor delay (below -2 standard deviations on standardized assessments
  • Face, motor, or reflex abnormalities

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Soo-Eun Chang, PhD contact

734-232-0300

sooeunc@umich.edu

Emily Garnett, PhD contact

734-232-3371

emilyog@umich.edu

United States1 site, 1 recruiting
  • University of Michigan

    Ann Arbor, Michigan, 48109

    Soo-Eun Chang, PhD, 734-232-0300, sooeunc@umich.edu

    Soo-Eun Chang, PhD

    Recruiting

Other trials in United States

About this study

Official title: Subcortical Network Connectivity and Temporal Processing in Children With Persistent and Recovered Stuttering

The specific purpose of this clinical trial is to compare performance on rhythm perception and production tasks between children who stutter and children who do not stutter. The overall project also aims to investigate how performance on rhythm tasks may be related to brain activity (non-clinical trial).

Read the detailed description

Participants in the clinical trial portion of this study will complete rhythm discrimination and finger tapping experiments once a year for 3 years. The study team will compare performance between groups. Participants will also participate in the non-trial portion of the project that includes having magnetic resonance imaging (MRI) each year for 3 years.

Being tested
Rhythm discrimination
Keywords
Rhythm, Temporal processing, Healthy children, Speech disorders, Timing
Medical subject headings
Stuttering, Speech Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Rhythm discriminationBehavioural

    Participants will complete a rhythm discrimination task once per year for 3 years.

Study groups in NCT05286151
Study groupRoleWhat they receive
Children who stutterExperimentalChildren who stutter
Receives: Behavioral: Rhythm discrimination
Children who do not stutterExperimentalChildren who do not stutter
Receives: Behavioral: Rhythm discrimination

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Rhythm discrimination (d')

    Performance on the rhythm discrimination task will be assessed using a signal detection analysis to distinguish between participants' ability to discriminate same and different rhythms from any general tendency to respond same or different. Hit rates (HRs) and false alarm rates (FARs) will be obtained to calculate d' (a measure of sensitivity; determined by z(HR) - z(FAR)).

    Measured: Year 1

  2. Rhythm discrimination (d')

    Performance on the rhythm discrimination task will be assessed using a signal detection analysis to distinguish between participants' ability to discriminate same and different rhythms from any general tendency to respond same or different. Hit rates (HRs) and false alarm rates (FARs) will be obtained to calculate d' (a measure of sensitivity; determined by z(HR) - z(FAR)).

    Measured: Year 2

  3. Rhythm discrimination (d')

    Performance on the rhythm discrimination task will be assessed using a signal detection analysis to distinguish between participants' ability to discriminate same and different rhythms from any general tendency to respond same or different. Hit rates (HRs) and false alarm rates (FARs) will be obtained to calculate d' (a measure of sensitivity; determined by z(HR) - z(FAR)).

    Measured: Year 3

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Mar 2022
  2. Study start23 Jul 2022
  3. Primary completion31 Jan 2028 (estimated)
  4. Study completion31 Jan 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05286151
Sponsor's protocol ID
HUM00196133
Other IDs
2R01DC011277
Status last verified
Oct 2026
First submitted
9 Mar 2022
Last updated
15 Oct 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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