Clinical trial Recruiting at 1 site Interventional Ages 7 to 17

Improving speech clarity in children with cerebral palsy using augmentative communication

Official title: Speech Supplementation Strategies for Improving Intelligibility in Children With Cerebral Palsy (CP)

Run by University of Wisconsin, Madison · NCT07173049 · Data updated 2026-11-12

This test checks whether having children with cerebral palsy point to letters or pictures while they speak can make their speech easier to understand.

Quick facts

Study typeInterventional
Ages7 Years to 17 Years
SexAll
Enrollment100 (estimated)
SponsorUniversity of Wisconsin, Madison
Academic / other
Locations1 site (Madison, Wisconsin)
StatusRecruiting
StartedJuly 27, 2026
Main results expectedMarch 2029
Study endsJuly 2029
Registry record updatedAugust 3, 2026
Trial IDNCT07173049 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Children aged 7–17 with a diagnosis of cerebral palsy (or a similar early-onset motor disorder), clinical dysarthria with intelligibility between 10–85%, ability to produce connected English speech of at least three words, ability to point with their hands, basic picture identification skills, and passing a hearing screen are ideal candidates.

Probably not a fit

Children who cannot see or point to items on a communication board, cannot produce connected English utterances of at least three words, have intelligibility outside the 10–85% range, or have other clinical issues that make participation unsuitable are unlikely to benefit from this intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a one-session pre/post intervention with 100 children aged 7–17 who have cerebral palsy and dysarthria. Participants produce a baseline set of 60 sentences, receive one-on-one training from a speech-language pathologist in a speech supplementation AAC strategy (pointing to first letters or topical pictures while speaking), then produce the same sentences using the strategy. Post-test samples and a set of emphasized-word repetition tasks are played to blinded listeners who orthographically transcribe and score intelligibility in both habitual and supplemented conditions. The study compares intelligibility scores across conditions to determine how much change is needed for meaningful improvement.

Why it matters

Potential benefit: If successful, this approach could make everyday speech easier to understand for some children with cerebral palsy, improving communication with family, classmates, and caregivers.

How similar studies have gone: Related AAC and speech supplementation approaches have shown promise in prior smaller studies, but one-session effects on intelligibility in a larger pediatric CP sample are less well established.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Medical diagnosis of cerebral palsy, or a similar, related condition that affects early motor development and presents as a chronic motor disability
* Age between 7 and 17 years
* Clinical dysarthria with speech intelligibility between 10-85 percent
* Able to produce connected speech in English, with a minimum utterance length of 3 words
* Able to use hands to point to items on a communication board
* Cognitive/language skills that enable basic picture identification on a communication board
* Pass pure tone hearing screening

Exclusion Criteria:

* Failure to meet all inclusion criteria.
* Vision impairment that precludes being able to see items on a communication board.
* Not suitable for participation due to other reasons at the discretion of the investigators.

Where it's running

  • University of Wisconsin-Madison Waisman Center
    Madison, Wisconsin, United States
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.