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NCT04625062 · ClinicalTrials.gov registry record · Phase 1

Comparing Traditional and Biofeedback Telepractice Treatment for Residual Speech Errors

A Phase 1 study, sponsored by New York University.

Completed
Registry status
Phase 1
Development phase
7
Enrollment target

NCT04625062 is a Phase 1 study that has completed, run by New York University. The registered enrollment target is 7 participants.

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The verdict

NCT04625062, a Phase 1 study, has completed, sponsored by New York University.

COMPLETED
Registry status
Phase 1
Development phase
7 participants
Enrollment target

Study Summary

This study aims to evaluate the relative efficacy of biofeedback and traditional treatment for residual speech errors when both are delivered via telepractice. In a single-case randomization design, up to eight children with RSE will receive both visual-acoustic biofeedback and traditional treatment via telepractice. Acoustic measures of within-session change will be compared across sessions randomly assigned to each condition. It is hypothesized that participants will exhibit a clinically significant overall treatment response and that short-term measures of change will indicate that biofeedback is associated with larger increments of progress than traditional treatment.

Interventions

  • BEHAVIORAL Visual-acoustic biofeedback
  • BEHAVIORAL Motor-based treatment

Trial Details

FieldValue
Enrollment Target 7 participants
Start Date 2020-09-01
Est. Completion 2021-03-18
Phase Phase 1

Sponsor

New York University

83 total trials

What the Registry Record Tells You About NCT04625062

The ClinicalTrials.gov registry entry for NCT04625062 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 7 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is New York University, which has 83 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Visual-acoustic biofeedback is the first listed.

NCT04625062 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04625062 about?

NCT04625062 is a clinical study titled "Comparing Traditional and Biofeedback Telepractice Treatment for Residual Speech Errors". This study aims to evaluate the relative efficacy of biofeedback and traditional treatment for residual speech errors when both are delivered via telepractice. In a single-case randomization design, up to eight children with RSE will receive both visual-acoustic biofeedback and traditional treatment...

What is the current status of trial NCT04625062?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 7 participants. The study started on 2020-09-01. Estimated completion is 2021-03-18.

What interventions are being tested in trial NCT04625062?

The interventions under investigation include: Visual-acoustic biofeedback (BEHAVIORAL), Motor-based treatment (BEHAVIORAL).

Who is sponsoring clinical trial NCT04625062?

This trial is sponsored by New York University, which has 83 total clinical trials registered on ClinicalTrials.gov.

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

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