- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03101449
Analysis of the Effects of Vocal Conditioning Through Semi-occluded Vocal Tract Exercises in Choir Singers
March 30, 2017 updated by: Mauriceia Cassol, Federal University of Health Science of Porto Alegre
This research aims to evaluate the effects of vocal conditioning through two semioccluded vocal tract exercises (SOVTE) in choir singers.
Study Overview
Detailed 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.
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Rio Grande do Sul
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Porto Alegre, Rio Grande do Sul, Brazil, 90.050-170
- Federal University of Health Science of Porto Alegre
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- signing of the Informed Consent (IC).
Exclusion Criteria:
- voice disorders diagnosed by otolaryngologist physician;
- smokers;
- presence below 75% in the meetings.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group 1
20 individuals of Coral UFCSPA without voice problems carry out the exercise with Finnish tube before choir practice once a week for a period of 14 weeks.
The exercise will be carried out with blowing set to sound at regular frequency, with frequency variation and with the melody of "Happy Birthday"; each sequence will be held for 2 minutes with 1 minute interval between them.
|
Practice the exercise with Finnish tube before choir practice once a week for a period of 14 weeks.
|
|
Experimental: Group 2
20 individuals of Coral UFCSPA without voice problems carry out the exercise straw phonation before choir practice once a week for a period of 14 weeks.
The exercise will be carried out with blowing set to sound at regular frequency, with frequency variation and with the melody of "Happy Birthday"; each sequence will be held for 2 minutes with 1 minute interval between them.
|
Practice the exercise straw phonation before choir practice once a week for a period of 14 weeks.
|
|
No Intervention: Group 3
10 individuals of Coral UFCSPA without voice problems.
Untreated group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Voice quality
Time Frame: 3 months
|
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 Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mean fundamental frequency
Time Frame: 3 months
|
Improvement of acoustic parameters, demonstrated by VoxMetria software.
|
3 months
|
|
Jitter
Time Frame: 3 months
|
Improvement of acoustic parameters, demonstrated by VoxMetria software.
|
3 months
|
|
Shimmer
Time Frame: 3 months
|
Improvement of acoustic parameters, demonstrated by VoxMetria software.
|
3 months
|
|
Glottal to Noise Excitation (GNE)
Time Frame: 3 months
|
Improvement of acoustic parameters, demonstrated by VoxMetria software.
|
3 months
|
|
Profile vocal range
Time Frame: 3 months
|
Improved profile vocal range, shown by Vocalgrama software.
|
3 months
|
|
Maximun phonation time
Time Frame: 3 months
|
Improvement of maximum phonation time, demonstrated by measuring the maximum times of sustaining vowels and phonemes /s/ and /z/.
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2016
Primary Completion (Anticipated)
April 1, 2017
Study Completion (Anticipated)
July 1, 2017
Study Registration Dates
First Submitted
October 26, 2016
First Submitted That Met QC Criteria
March 30, 2017
First Posted (Actual)
April 5, 2017
Study Record Updates
Last Update Posted (Actual)
April 5, 2017
Last Update Submitted That Met QC Criteria
March 30, 2017
Last Verified
March 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- 50412515.9.0000.5345
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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