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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04096352
Other study ID # VirtuVox2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 29, 2019
Est. completion date February 20, 2020

Study information

Verified date April 2020
Source University of Liege
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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).


Recruitment information / eligibility

Status Completed
Enrollment 41
Est. completion date February 20, 2020
Est. primary completion date February 20, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Direct Method
Learning effective vocal skills using speech therapy exercises and virtual reality simulations.
Indirect Method
Information on voice function and voice hygiene.

Locations

Country Name City State
Belgium Université de Liège Liège Wallonia

Sponsors (2)

Lead Sponsor Collaborator
University of Liege Universite du Quebec en Outaouais

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Self-perceived voice changes between the baseline and the end of the intervention Self-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. 3 weeks
Primary Voice frequency changes between the baseline and the end of the intervention Acoustic measurements of participants' voice frequency (in hertz) when speaking with and without background noise. 3 weeks
Primary Voice intensity changes between the baseline and the end of the intervention Acoustic measurements of participants' voice intensity (in dB) when speaking with and without background noise. 3 weeks
Primary Voice spectrum changes between the baseline and the end of the intervention Acoustic measurements of participants' voice spectrum (in Hertz) when speaking with and without background noise. 3 weeks
Primary Speech rate changes between the baseline and the end of the intervention Measurements of participants' speech rate (in syllables per second) when speaking with and without background noise. 3 weeks
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