ClinicalTrials.Veeva

Menu

Evaluating the Efficacy of Opti-Speech for Speech Treatment

V

Vulintus

Status

Completed

Conditions

Prelingual Deafness
Dysarthria
Articulation Disorder

Treatments

Device: Opti-Speech

Study type

Interventional

Funder types

Other
Industry
NIH

Identifiers

NCT02705326
2R44DC013467 (U.S. NIH Grant/Contract)
VUL_2R44DC013467_OptiSpeech

Details and patient eligibility

About

The purpose of this study is to determine if feedback from a three-dimensional real-time visualization of the tongue, a program called Opti-Speech, can be used to improve speech.

Full description

Participants will be asked to complete the Goldman Fristoe Test of Articulation along with several other assessment tests. Then speech treatment, guided by Opti-Speech, will be provided to the participant for up to 10 treatment sessions. The participant will be asked to come back after the final treatment for a 2-month follow-up assessment.

Enrollment

37 patients

Sex

All

Ages

12 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • English speaking individuals with speech errors resulting from persistent speech sound disorder, individuals with dysarthria resulting from neurological disorders and individuals with pre-lingual or congenital deafness.

Exclusion criteria

  • Cognitive impairments that affect their ability to understand and follow instructions by the treating speech language pathologists

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

37 participants in 1 patient group

Opti-Speech
Experimental group
Description:
Speech treatment will be guided by Opti-Speech's visual feedback of tongue movement during speech
Treatment:
Device: Opti-Speech

Trial contacts and locations

2

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems