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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03101449
Other study ID # 50412515.9.0000.5345
Secondary ID
Status Active, not recruiting
Phase N/A
First received October 26, 2016
Last updated March 30, 2017
Start date March 2016
Est. completion date July 2017

Study information

Verified date March 2017
Source Federal University of Health Science of Porto Alegre
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This research aims to evaluate the effects of vocal conditioning through two semioccluded vocal tract exercises (SOVTE) in choir singers.


Description:

This research aims to evaluate the effects of vocal conditioning through two semioccluded vocal tract exercises (SOVTE) - Finnish tube and phonation in high strength straw - in vocal parameters, vocal extension profile and maximum phonation time for a period of four months in a group of singers. acoustic analysis will be performed of the average parameters of the fundamental frequency (F0), jitter, shimmer and glottal to Noise Excitation (GNE) by VoxMetria program and perceptual analysis through Consensus Assessment Perceptual Hearing the Voice Protocol (CAPE-V) three times: before the vocal conditioning, after the last meeting of the technical realization and a week after the vocal conditioning period.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 30
Est. completion date July 2017
Est. primary completion date April 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- signing of the Informed Consent (IC).

Exclusion Criteria:

- voice disorders diagnosed by otolaryngologist physician;

- smokers;

- presence below 75% in the meetings.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Finnish tube
Practice the exercise with Finnish tube before choir practice once a week for a period of 14 weeks.
Staw phonation
Practice the exercise straw phonation before choir practice once a week for a period of 14 weeks.

Locations

Country Name City State
Brazil Federal University of Health Science of Porto Alegre Porto Alegre Rio Grande do Sul

Sponsors (1)

Lead Sponsor Collaborator
Federal University of Health Science of Porto Alegre

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Voice quality Improved singing voice quality standard demonstrated by the perceptual analysis of voice with CAPE- V, in which there is a decrease in score value pre and post intervention. 3 months
Secondary Mean fundamental frequency Improvement of acoustic parameters, demonstrated by VoxMetria software. 3 months
Secondary Jitter Improvement of acoustic parameters, demonstrated by VoxMetria software. 3 months
Secondary Shimmer Improvement of acoustic parameters, demonstrated by VoxMetria software. 3 months
Secondary Glottal to Noise Excitation (GNE) Improvement of acoustic parameters, demonstrated by VoxMetria software. 3 months
Secondary Profile vocal range Improved profile vocal range, shown by Vocalgrama software. 3 months
Secondary Maximun phonation time Improvement of maximum phonation time, demonstrated by measuring the maximum times of sustaining vowels and phonemes /s/ and /z/. 3 months
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