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Clinical Trials/NCT01097161
NCT01097161
Completed
N/A

The Speech Prosody of People With Stuttering and Developmental Apraxia: the Efficacy of an Intervention Program

Federal University of Minas Gerais1 site in 1 country4 target enrollmentApril 2007

Overview

Phase
N/A
Intervention
Not specified
Conditions
Stuttering
Sponsor
Federal University of Minas Gerais
Enrollment
4
Locations
1
Status
Completed
Last Updated
16 years ago

Overview

Brief Summary

Subjects' utterances were submitted to acoustic analysis before and after the intervention program applied on prosodic basis.

Detailed Description

The study has the aim of developing knowledge, methodology and technique in the prosody area, for its application on the speech therapy, with the assistance of a feedback system - with WinpitchPro (Philippe Martin). A database was constituted on the basis of a patterned corpus (EUROM1) by its translation, recording and editing on .wav format. Throughout model-sentences, an experimental intervention program initiates with the participation of 2 adults with stuttering problem and 2 with apraxia of speech. The efficacy of the therapeutic procedure is tested on the basis of the acoustical and the statistical analyses which have compared the first and the second speech samples taken before and after the twenty (20) therapy sessions held in a prosody approach only.

Registry
clinicaltrials.gov
Start Date
April 2007
End Date
June 2008
Last Updated
16 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Federal University of Minas Gerais

Eligibility Criteria

Inclusion Criteria

  • Clinical diagnosis of stuttering
  • Clinical diagnosis of apraxia of speech
  • 18 years of age or older
  • Portuguese native language
  • Agreement by the participant to enroll on 20 therapy sessions scheduled in a 3 month period

Exclusion Criteria

  • History of major medical illness unrelated to primary diagnosis of developmental stuttering and developmental apraxia of speech
  • Significant abnormalities on general physical and neurological examination unrelated to primary diagnosis

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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