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Virtual Reality in Teachers' Vocal Motor Behavior Acquisition (VirtuVox)

Virtual Reality in Teachers' Vocal Motor Behavior Acquisition (VirtuVox): Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04096352
Acronym
VirtuVox
Enrollment
41
Registered
2019-09-19
Start date
2019-09-29
Completion date
2020-02-20
Last updated
2020-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Virtual Reality Therapy, Voice Disorders

Keywords

Speech Therapy, Virtual Reality, Teacher's voice, Background Noise, School Teachers

Brief summary

Scientific literature supports that teachers are at greater risk for voice disorders than the general population. In the classroom, the teacher's voice represents the main communication tool. Optimal voice use is indispensable to ensure effective teaching and preserve the teacher's vocal health. This project investigates how virtual reality (VR) facilitates the learning of effective vocal skills and their application in real-world contexts. Based on acoustic analyses and self-assessment scales, the investigators compare 100 future teachers randomly assigned in two groups. The experimental group (n=50) receives a voice training by VR simulations and voice information. The control group (n=50) only receives voice information.

Detailed description

Experimental group participants receive direct method (three 1-hour sessions of voice training by virtual reality simulations over a course of 3 weeks) and indirect method (one 1-hour session of information on voice function and voice hygiene). Control group participants receive indirect method (one 1-hour session of information on voice function and voice hygiene).

Interventions

BEHAVIORALDirect Method

Learning effective vocal skills using speech therapy exercises and virtual reality simulations.

BEHAVIORALIndirect Method

Information on voice function and voice hygiene.

Sponsors

Universite du Quebec en Outaouais
CollaboratorOTHER
University of Liege
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* future teacher having completed at least one internship as a schoolteacher * speaking French fluently

Exclusion criteria

* hearing impairment * voice pathology at the time of the study

Design outcomes

Primary

MeasureTime frameDescription
Self-perceived voice changes between the baseline and the end of the intervention3 weeksSelf-assessment of perceived vocal effort using the Adapted BORG Category Ratio (CR-10) physical exertion scale. On the scale, verbal expressions regarding vocal effort are anchored to the correct positions on a logarithmic ratio scale from zero (No vocal effort at all) to 10 (Maximum vocal effort), according to their quantitative meaning.
Voice frequency changes between the baseline and the end of the intervention3 weeksAcoustic measurements of participants' voice frequency (in hertz) when speaking with and without background noise.
Voice intensity changes between the baseline and the end of the intervention3 weeksAcoustic measurements of participants' voice intensity (in dB) when speaking with and without background noise.
Voice spectrum changes between the baseline and the end of the intervention3 weeksAcoustic measurements of participants' voice spectrum (in Hertz) when speaking with and without background noise.
Speech rate changes between the baseline and the end of the intervention3 weeksMeasurements of participants' speech rate (in syllables per second) when speaking with and without background noise.

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026