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Behavioural Intervention
Experimental and Reference Devices for Communication for Speech Disorder
N/A
Waitlist Available
Led By Gianluca DeLuca
Research Sponsored by Altec Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 30 mins to 2 hours
Awards & highlights
No Placebo-Only Group
Summary
This trial will test MyoVoice, a device that helps people who can't speak naturally by using muscle signals to create speech. It targets patients who lost their voice due to cancer surgery. MyoVoice works by reading muscle signals when someone mouths words and turning those signals into speech. The trial will compare MyoVoice to other speech aids to see how well it works and how easy it is to use.
Eligible Conditions
- Speech Disorder
- Speech Disorders in Children
- Speech and Language Therapy
- Alaryngeal Speech
- Assistive Communication Devices
- Speech Perception
- Speech Clarity
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 30 mins to 2 hours
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~30 mins to 2 hours
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Loudness Recognition Accuracy
Pitch Recognition Accuracy
Speech Naturalness
Secondary study objectives
Acceptability
Acoustic Identity
Emotional Content
+2 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Experimental and Reference Devices for CommunicationExperimental Treatment2 Interventions
Each participant listens to speech produced by an experimental ("MyoVoice") and reference (electrolarynx) systems that are used to communicate. Participants rate the naturalness of the speech produced from each device (audio files presented in a randomized order). Duration: 30 mins to 1 hour.
Group II: Development of Speech CorporaActive Control1 Intervention
Each participant produces a list of speech tasks that include syllables, phrases, reading passages, and open-ended questions using the MyoVoice system. Myovoice pitch and loudness recognition accuracy of speech is evaluated. Duration: 30 mins to 2 hours.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Experimental System: MyoVoice
2021
N/A
~30
Reference System: Electrolarynx
2021
N/A
~30
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Who is running the clinical trial?
Altec Inc.Lead Sponsor
4 Previous Clinical Trials
80 Total Patients Enrolled
Gianluca DeLucaPrincipal InvestigatorAltec Inc.
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