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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01196611
Other study ID # ETIC 0521.0.203.000-09
Secondary ID
Status Completed
Phase N/A
First received September 3, 2010
Last updated March 28, 2017
Start date September 2010
Est. completion date March 2013

Study information

Verified date September 2010
Source Federal University of São Paulo
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study compares two different approaches of voice therapy. Vocal Functional Exercises (Stemple,1997) and Voice Amplification using a portable amplifier (Tsi Supervoz II - Tecnisystem do Brasil TSI 1210).


Description:

Both approaches combined with Vocal Hygiene Program (Behlau, 2007).The target population are female teachers because they have the highest risk for developing voice problems. For this study the investigators are primarily interested in seeing if Vocal Functional Exercises and Voice Amplification are equally effective at improving vocal functioning in teachers with voice disorders. The Fiberoptic endoscopic evaluation will be done before randomization. All the participants will complete before and after a 6-week treatment phase (a) Voice Activity and Participation Profile (PPAV), an instrument designed to appraise the self-perceived psychosocial consequences of voice disorders to assess the impact of voice disorders on daily activities (b) Audio voice recording for later acoustic analysis, through the Kay Elemetrics Multi Dimensional Voice Program (c) Audio recording for later perceptual analysis through Consensus Auditory-Perceptual Evaluation of Voice (CAPE_V). It is believed that the search for evidence in clinical studies like this can contribute to awareness programs and vocal training for teachers.


Recruitment information / eligibility

Status Completed
Enrollment 162
Est. completion date March 2013
Est. primary completion date September 2012
Accepts healthy volunteers No
Gender Female
Age group 21 Years to 50 Years
Eligibility Inclusion Criteria:

- Female teacher

- 21-50 years old.

- Full or part time elementary to middle school teacher ( Prefeitura Municipal de Belo Horizonte).

- Minimum 20 hour weekly workload.

- Medical reference to speech therapy due to behavioral dysphonia

Exclusion Criteria:

- Physical education or daycare teachers.

- Professional singers.

- Neurological and/or psychiatric voice disorders

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Voice Amplification
Behavioral: Voice Amplification. Patients use VA over a course of 6 weeks Control group. No treatment over a course of 6 weeks.
Function Voice Exercises
Function Voice Exercises Patients will receive 6 sessions of therapy over a course of 6 weeks, with one session per week.

Locations

Country Name City State
Brazil Universidade Federal de Sao Paulo Sao Paulo

Sponsors (2)

Lead Sponsor Collaborator
Federal University of São Paulo Federal University of Minas Gerais

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fiberoptic endoscopic evaluation One year
Primary Score(CAPE_V); score(PPAV); score on acoustic analysis One year
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