iPad Application to Treat Prosodic Deficits in Students With Communication Disorders

Sponsor
Yale University (Other)
Overall Status
Completed
CT.gov ID
NCT01917864
Collaborator
Handhold Adaptive (Other)
200
1
1
34
5.9

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the utility of a specialized iPad application designed to treat difficulties with intonation (e.g., melody in voice) in children with autism spectrum disorders (ASD) and other communication disorders.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: iPad Application
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Handheld Technology for Speech Development in Students With Autism Spectrum Disorders
Study Start Date :
Jul 1, 2013
Actual Primary Completion Date :
May 1, 2016
Actual Study Completion Date :
May 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: iPad Application

Student participants will use specialized iPad software under the supervision of a speech-language pathologist over the course of 12 months, approximately one session per week, one hour per session.

Behavioral: iPad Application
A specialized iPad application, entitled SpeechPrompts, has been developed to treat prosodic difficulties commonly seen in ASDs. SpeechPrompts provides the SLPs that work with students with ASDs an additional tool to treat prosody. The SpeechPrompts software offers visual support and biofeedback to change prosody. These two tools are not typically available for school-based SLPs.

Outcome Measures

Primary Outcome Measures

  1. Effectiveness of software [12 months]

    The effectiveness of the software will be measured in two ways. Perceptual ratings of prosody. Pre- and post-treatment speech samples will be collected from each student participant. These samples will be rated by a member of the research staff on the following prosodic characteristics: rate, rhythm, stress, volume. Questionnaires. Questionnaires will be completed pre- and post-treatment by the students' classroom teacher and speech-language pathologist. These questionnaires will measure the students' use and generalization of skills taught during the intervention.

Secondary Outcome Measures

  1. Usability of software [12 months]

    Usability of software will be measured through questionnaires completed by the speech-language pathologists. Questionnaires will measure ease of software use, utility of software functions, and student engagement during intervention sessions.

  2. Student engagement in treatment [12 months]

    Student engagement will be evaluated indirectly by rating scales completed by the speech-language pathologist. Likert scales will be used to quantify student engagement on the following parameters: time engaged in on-task behavior, time engaged in off-task behavior, perceived enjoyment of software.

  3. Improvement in peer acceptance [12 months]

    Changes in peer acceptance will be evaluated using two different methodologies. Classroom teacher questionnaire. Each student's classroom teacher will complete a questionnaire pre- and post-treatment measuring the student's interaction with classroom peers. Semi-structured observation. A member of the research staff will observe each student pre- and post-treatment and complete frequency tallies on the number of peer interactions initiated during a 15-minute semi-structured activity.

Eligibility Criteria

Criteria

Ages Eligible for Study:
4 Years to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • SLPs, in Connecticut Public Schools, who provide intervention to students with autism spectrum disorders and related disorders

  • Students, ages 4-18, who attend school in Connecticut and demonstrate prosodic difficulties secondary to a diagnosis of ASD, apraxia of speech, or other communication disorder

Exclusion Criteria:
  • Students with concomitant genetic disorders

Contacts and Locations

Locations

Site City State Country Postal Code
1 Yale Child Study Center New Haven Connecticut United States 06510

Sponsors and Collaborators

  • Yale University
  • Handhold Adaptive

Investigators

  • Principal Investigator: Frederick Shic, Ph.D, Yale University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Yale University
ClinicalTrials.gov Identifier:
NCT01917864
Other Study ID Numbers:
  • 1306012259
  • ED-IES-13-R-0005
First Posted:
Aug 7, 2013
Last Update Posted:
Jun 14, 2016
Last Verified:
Jun 1, 2016

Study Results

No Results Posted as of Jun 14, 2016