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CompletedNCT02847923Updated Jul 28, 2016

Software for Alternative Communication

An interventional study of Presentation of alternative communication application and Familiarization with the software interface in Speech Impairment, sponsored by University of Mogi das Cruzes. Completed at 2 sites in Brazil. Open to participants aged 12 Years and older. Per ClinicalTrials.gov, last updated 2016-07-28.

Sponsored by University of Mogi das Cruzes · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Not applicable
Ages
12 Years and older
Sex
All
01

Study summary

The aim of this study is evaluate a software developed for alternative communication designed for people with speech difficulties. The software was executed by 30 volunteers using mobile devices that helped to play the scenarios simulated of communication situations.

Read the detailed description

Communication is a fundamental element that contributes to the development of the human being, promoting their coexistence in society. However, several factors, among them the Cerebral palsy (CP), can cause changes in muscle tone, causing injury in phono-articulatory which prevent or impair the speech production. This research aims to the development of a mobile application to promote the augmentative and alternative communication for people with CP, which adapt to the characteristics of motor limitations of these users. A mobile application was developed with pictographic resources and a voice synthesis engine, which can be customized according to the level of motor impairment and need for communication of the user. Were recruited 30 volunteers with CP who have speech difficulties and motor impairment. By means of a test script, these volunteers have used the mobile application and evaluated their usability using the questionnaire System Usability Scale (SUS), which contains 10 questions related to the ease of learning, efficiency, ease of memorization, occurrence of runtime errors of execution and level of user satisfaction.

02

Conditions studied

  • Speech Impairment

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Keywords

  • Mobile Devices
  • Augmentative and Alternative Communication
  • Cerebral Palsy
03

In context

Speech Disorders

65 studies on the registry are indexed under Speech Disorders; 23 are open to participants now.

This study's enrollment of 30 is below the median of 44 across 45 interventional studies indexed under Speech Disorders.

Browse Speech Disorders studies →

Lead sponsor

University of Mogi das Cruzes is the lead sponsor of 16 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
12 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Cerebral Palsy and speech disorder

Exclusion criteria

Exclusion Criteria:

  • visual impairment and / or severe cognitive impairment
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    Group Experimental

    All the volunteers will use the software and then answer the questionnaire. They will be familiar with the software interface, performs an initial test to learn how to use the software, run a test script and answer the questionnaire.

    Other: Presentation of alternative communication application · Other: Familiarization with the software interface · Other: Test of the software · Other: Answer the questionnaire

Interventions

  • OtherPresentation of alternative communication application

    At this stage the purpose of the application is submitted, what its purpose and its features in a brief and clear manner.

  • OtherFamiliarization with the software interface

    At this stage, the volunteer will be asked to use the application by himself for a short time so that he can get acquainted and learn to use it

  • OtherTest of the software

    Then, the volunteer is instructed to use the application following a script task that will expose a simple and fast way all the application features. These tasks have easy actions to be executed, for example: The user must communicate through the application the phrase "I want to drink water," so that he will be instructed to perform the actions to select the option and then drink the water option.

  • OtherAnswer the questionnaire

    After performing all the tasks the user replies to a questionnaire to evaluate the usability of the application after you use.

06

What researchers measure

Primary outcomes

  1. Questionnaire

    Questionnaire based in System Usability Scale (SUS) with 10 item questionnaire and five response options for respondents. Each response can be chosen in range: totally disagree, disagree, neither agree nor disagree, agree and totally agree.

    Time frame: 15 minutes

07

Study locations

2 sites
  • Cid Torquato
    Mogi das Cruzes, São Paulo, Brazil
  • Sesi Suzano
    Suzano, São Paulo 08673-270, Brazil
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 28, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02847923
Lead sponsor
University of Mogi das Cruzes
Collaborators
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior., Instituto Federal de Educação, Ciência e Tecnologia de São Paulo - IFSP
Responsible party
Flavio Cezar Amate (Research Professor, University of Mogi das Cruzes) — Principal investigator
First posted
Jul 28, 2016
Start date
Oct 2015
Primary completion
Oct 2015
Completion
Nov 2015
Last update
Jul 28, 2016

Study contacts

Flávio C Amate, Dr
principal investigator · Núcleo de Pesquisas Tecnologicas - NPT/UMC

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2016. You cannot join it, but the record below documents what was studied.

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