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NCT06517225 · ClinicalTrials.gov registry record · Phase 2
Visual-acoustic Intervention With Service Delivery In-person and Via Telepractice Trial
A Phase 2 study of Speech Sound Disorder, sponsored by New York University.
- Recruiting
- Registry status
- Phase 2
- Development phase
- 76
- Enrollment target
- 3
- Study locations
NCT06517225: Recruiting Phase 2 study of Speech Sound Disorder, sponsored by New York University.
NCT06517225 is a Phase 2 study of Speech Sound Disorder that is actively recruiting participants, run by New York University. The registered enrollment target is 76 participants, below the 84-participant average among 15 other Speech Sound Disorder trials with a reported enrollment target (10% lower). The trial reports 3 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06517225, a Phase 2 study of Speech Sound Disorder, is actively recruiting participants, sponsored by New York University.
- RECRUITING
- Registry status
- Phase 2
- Development phase
- 76 participants
- Enrollment target
- 3
- Study locations
Study Summary
Children with speech sound disorder show diminished intelligibility in spoken communication and may thus be perceived as less capable than peers, with negative consequences for both socioemotional and socioeconomic outcomes. New technologies have the potential to transform interventions for speech sound disorder, but there is a lack of rigorous evidence to substantiate this promise. This research will meet a public health need by systematically evaluating the efficacy of visual-acoustic biofeedback intervention delivered in-person versus via telepractice. The objective of this study is to test the hypothesis that treatment incorporating visual-acoustic biofeedback can be delivered via telepractice without a significant loss of efficacy. Participants will be randomly assigned to receive identical treatment either via online telepractice or in the laboratory setting. The same software for visual-acoustic biofeedback, staRt, will be used in both conditions. Participants' progress in treatment will be evaluated based on blinded listeners' perceptual ratings of probes produced before and after treatment. Pre and post treatment evaluations will be carried out in person for all participants.
Primary Outcome
To assess generalization of treatment gains to untreated words, participants will be assessed with standard probes (30 words \[considered the primary target\], 20 syllables, and 10 sentences containing /r/ in various phonetic contexts). Stimuli in each probe will be presented individually in randomized order with blocking by stimulus type (word, syllable, sentence). Individual words will be isolated from the audio record of each word probe and presented in randomized order for binary rating (cor
Conditions Studied
Interventions
- BEHAVIORAL Visual-acoustic biofeedback
Study Locations (3)
New York
- New York University - New York
- Syracuse University - Syracuse
New Jersey
- Montclair State University - Bloomfield
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 76 participants |
| Start Date | 2024-07-01 |
| Est. Completion | 2028-12-31 |
| Phase | Phase 2 |
What NCT06517225 shows while recruiting
NCT06517225 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 76 participants, a relatively small participant target, below the 84-participant average among 15 other Speech Sound Disorder trials with a reported enrollment target (10% lower).
The record links to 1 condition, with Speech Sound Disorder appearing as the primary indexed condition, and to 1 intervention - of which Visual-acoustic biofeedback is the first listed.
NCT06517225 reports a single indexed study location in New York, New Jersey.
Frequently Asked Questions
What is clinical trial NCT06517225 about?
NCT06517225 is a clinical study titled "Visual-acoustic Intervention With Service Delivery In-person and Via Telepractice Trial". Children with speech sound disorder show diminished intelligibility in spoken communication and may thus be perceived as less capable than peers, with negative consequences for both socioemotional and socioeconomic outcomes. New technologies have the potential to transform interventions for speech s...
What is the current status of trial NCT06517225?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 76 participants. The study started on 2024-07-01. Estimated completion is 2028-12-31.
What conditions does trial NCT06517225 study?
This clinical trial studies the following conditions: Speech Sound Disorder.
What interventions are being tested in trial NCT06517225?
The interventions under investigation include: Visual-acoustic biofeedback (BEHAVIORAL).
Who is sponsoring clinical trial NCT06517225?
This trial is sponsored by New York University, which has 83 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06517225 being conducted?
This trial has 3 study locations across New Jersey, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Speech Sound Disorder
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06517225's enrollment target sits among peer trials
76 6th of 15 higher than 9 of 15 other Speech Sound Disorder trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Speech Sound Disorder trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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