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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02069795
Other study ID # IRB # 1312958125
Secondary ID
Status Completed
Phase N/A
First received February 17, 2014
Last updated March 14, 2016
Start date February 2014
Est. completion date August 2014

Study information

Verified date March 2016
Source Methodist Sports Medicine
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The waveform assessment of an athlete's speech production has a high probability of showing abnormalities after brain injury (concussions) which could be used not only for diagnosis of the concussion, but for recovery of the brain. The aim of this study is to investigate this possibility using the Cobweb automated application system for acoustic processing.


Description:

Concussions affect cognitive and fine muscle motor control, and these changes will be reflected in the acoustic characteristics of the vowels being produced. The methods to identify and analyze the acoustics of vowels will greatly extend the detailed understanding of vowels produced after a concussion. The identification of the changes in formant frequencies, pitch, and duration will provide the means to use these parameters as an automated diagnostic tool. The waveform assessment of the athlete's speech production has a high probability of showing brain abnormalities immediately after a suspected or diagnosed concussion at the venue of the athletic sport. The aim of this study assessment is to investigate this possibility using the Cobweb system and greatly enhance the ability to diagnose a concussion in a timely manner to remove the athlete from practice or play.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date August 2014
Est. primary completion date August 2014
Accepts healthy volunteers No
Gender Both
Age group 6 Years to 21 Years
Eligibility Inclusion Criteria:

- All patients diagnosed or suspected of having a sports concussion seen in a clinical setting

- Ages 6 -21

Exclusion Criteria:

- Patients who have physical injuries to their lips, tongue or oral cavity will be excluded until they have healed.

- Patients with hearing or speech abnormalities who cannot consistently produce the stimulus materials.

- Non-native speakers who cannot read the materials or produce the stimuli consistently.

- Patients who cannot read the materials or produce the stimuli consistently due to their age.

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Other:
Voice recording


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Methodist Sports Medicine Waveform Communications LLC

Outcome

Type Measure Description Time frame Safety issue
Primary Change in formant frequencies 1. Changes in formant frequencies F0,F1,F2,F3 in patients following concussion to recovery time. 2 months No
Secondary Changes in duration of speech production Changes in duration of speech production in patients following concussion to recovery time . 2 months No
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