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NCT07061730 · ClinicalTrials.gov registry record · NA

Evaluating the Effectiveness of Hybrid and Traditional Speech Therapy for /ɹ/ and /s/ Sound Production

A NA study of Speech Sound Disorder, sponsored by Syracuse University.

Recruiting
Registry status
NA
Development phase
120
Enrollment target
1
Study location

NCT07061730 is a NA study of Speech Sound Disorder that is actively recruiting participants, run by Syracuse University. The registered enrollment target is 120 participants, above the 81-participant average among 15 other Speech Sound Disorder trials with a reported enrollment target (48% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT07061730, a NA study of Speech Sound Disorder, is actively recruiting participants, sponsored by Syracuse University.

RECRUITING
Registry status
NA
Development phase
120 participants
Enrollment target
1
Study location

Study Summary

The purpose of this research study is to evaluate the effectiveness of a hybrid Artificial Intelligence-assisted speech therapy model, which combines the use of an AI speech therapist (Jessica) with traditional speech therapy sessions led by a Speech-Language Pathologist (SLP). This study aims to determine whether the hybrid model improves articulation in children more effectively than traditional SLP-only therapy. Over the course of 8 weeks, participants will receive weekly therapy sessions, and those in the hybrid therapy group will also practice with Jessica between sessions. The study will also gather feedback from parents and speech therapists to assess their experiences and satisfaction with treatment.

Conditions Studied

Interventions

  • BEHAVIORAL Traditional Therapy
  • BEHAVIORAL Hybrid therapy

Study Locations (1)

New York

  • Syracuse University - Syracuse

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2025-05-01
Est. Completion 2026-02
Phase NA

Sponsor

Syracuse University

31 total trials

What the Registry Record Tells You About NCT07061730

The ClinicalTrials.gov registry entry for NCT07061730 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 81-participant average among 15 other Speech Sound Disorder trials with a reported enrollment target (48% higher). The listed sponsor is Syracuse University, which has 31 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Speech Sound Disorder appearing as the primary indexed condition, and to 2 interventions - of which Traditional Therapy is the first listed.

NCT07061730 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT07061730 about?

NCT07061730 is a clinical study titled "Evaluating the Effectiveness of Hybrid and Traditional Speech Therapy for /ɹ/ and /s/ Sound Production". The purpose of this research study is to evaluate the effectiveness of a hybrid Artificial Intelligence-assisted speech therapy model, which combines the use of an AI speech therapist (Jessica) with traditional speech therapy sessions led by a Speech-Language Pathologist (SLP). This study aims to de...

What is the current status of trial NCT07061730?

This trial is currently recruiting. It is a NA study. The enrollment target is 120 participants. The study started on 2025-05-01. Estimated completion is 2026-02.

What conditions does trial NCT07061730 study?

This clinical trial studies the following conditions: Speech Sound Disorder.

What interventions are being tested in trial NCT07061730?

The interventions under investigation include: Traditional Therapy (BEHAVIORAL), Hybrid therapy (BEHAVIORAL).

Who is sponsoring clinical trial NCT07061730?

This trial is sponsored by Syracuse University, which has 31 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07061730 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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