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Clinical Trials/NCT02935062
NCT02935062
Completed
N/A

New Therapeutical Perspectives in Cases of Phonological Disorders

Universidade Federal de Santa Maria2 sites in 1 country24 target enrollmentJuly 2016

Overview

Phase
N/A
Intervention
Not specified
Conditions
Speech Sound Disorders
Sponsor
Universidade Federal de Santa Maria
Enrollment
24
Locations
2
Primary Endpoint
Percentage of Consonants Correct (PCC) Pre-treatment and Post-treatment Phonological Instrument
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The aim of this study is to verify phonological and auditory aspects of children submitted to traditional phonological therapy, phonological therapy using a software and placebo therapy in children with phonological disorders.

Detailed Description

The study will provide different therapeutic approaches for cases of phonological disorders, the classical approach would be mediated by Cycles Model, innovated approach is performed by means of an intervention speech software-SIFALA, there will still be the group that does not receive any of the proposals therapies that will be the placebo group.The study will provide 25 sessions for each group, with 30 minutes in each group. At the end of these sessions, the placebo group will receive one of the therapeutic approaches. With these three study groups, the investigators understand in what manner to obtain correct sounds is more effective.

Registry
clinicaltrials.gov
Start Date
July 2016
End Date
February 2018
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Marcia Keske Soares

Professora Doutora

Universidade Federal de Santa Maria

Eligibility Criteria

Inclusion Criteria

  • Parents/guardians and child agree to participate and have signed the Informed Consent Form;
  • Have age between 4:0 to 8:11 (years:months);
  • Present diagnosis of phonological disorders;
  • Present hearing thresholds within the normal range

Exclusion Criteria

  • Present neurological impairment, emotional and/or cognitive clearly diagnosed, or have complaint;
  • Present any degree of hearing loss is the type conductive, mixed or sensorineural, and middle ear disorders in time of selection, as well as having presented otitis complaints;
  • Present language impairment associated with speech sound disorder;
  • Present commitment in the stomatognathic system that can interfere in the speech production;
  • Have been received speech and language therapy before.

Outcomes

Primary Outcomes

Percentage of Consonants Correct (PCC) Pre-treatment and Post-treatment Phonological Instrument

Time Frame: 10 weeks

The percentage of correct consonants corresponds to the number of phonemes produced by the child, evaluated initially before starting treatment and at the end of treatment. The variable of this calculation is based on the percentage which is determined at what phonological level of disorder the child is at. It is expected that at the end of treatment the percentage of correct consonants will increase due to the therapy stimuli offered.

P300- Long-latency Auditory Evoked Potential

Time Frame: 10 weeks.

Electrophysiological evaluation of the auditory pathway through the protocol, Pretreatment and Post-treatment P300 waves were analyzed by the latency according to the parameters of MacPherson (1996). The electrophysiological protocol was performed before and after therapy. The marking of the waves was judged by specialist judges in the field of audiology. The variable that predicts P300 latency is quantified in milliseconds (ms

Study Sites (2)

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