RoboHear™ Device: Advanced Haptic Technology That Allows the Deaf to Understand Speech

NCT ID: NCT03966144

Last Updated: 2020-05-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2020-03-25

Study Completion Date

2020-03-25

Brief Summary

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Pilot study to test the feasibility of translating the English language into haptics (touch sensations)

Detailed Description

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An adaptive pilot trial of RoboHear™ hardware and software to test the feasibility of learning to understand language using a haptic (touch) device installed in the stem of a pair of glasses. These tests are not meant to be exhaustive but will validate the hardware and software and provide an informal test platform for learning to 'hear' or interpret sounds and words using haptic technology.

Conditions

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Hearing Impairment Deafness

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Participants will undergo computer based testing using the device to determine the number of haptic stimuli that are correctly interpreted as phenomes.
Primary Study Purpose

DEVICE_FEASIBILITY

Blinding Strategy

NONE

Study Groups

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RoboHear Device

Subjects will wear the Robo-Hear device and receive haptic stimuli. They will be tested on their ability to interpret these haptic sensations as sounds and words.

Group Type EXPERIMENTAL

RoboHear Device

Intervention Type DEVICE

Delivery of haptic sensations followed by testing to assess the ability to interpret stimuli as sounds and words

Interventions

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RoboHear Device

Delivery of haptic sensations followed by testing to assess the ability to interpret stimuli as sounds and words

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Participants need to understand English.
* Participants must be able to sit at a computer for the training and evaluation session. The session may range from one hour to up to 4 hours in length (with breaks provided as needed).

Exclusion Criteria

* Inability to understand English
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Arkansas

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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John L Dornhoffer, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Arkansas

Locations

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University of Arkansas for Medical Sciences

Little Rock, Arkansas, United States

Site Status

Countries

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United States

Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

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228355

Identifier Type: -

Identifier Source: org_study_id

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