Visual and Auditory Breathing-swallowing Coordinated Training

NCT ID: NCT04590391

Last Updated: 2021-09-05

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

COMPLETED

Clinical Phase

NA

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-12-01

Study Completion Date

2021-03-31

Brief Summary

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Dysphagia is caused by multiple factors, and respiratory-swallowing discoordination is considered to be one of the factors. The investigators recently developed a visual and auditory breathing-swallowing coordinated training device. In this study, investigators examined the validity of a this device for healthy subjects. The investigators will examine which respiratory phase the swallowing occurs when the swallowing is started in accordance with the signal lighting and voice of this device.

Detailed Description

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Conditions

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Breathing-Swallowing Coordination Dysphagia Rehabilitation

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DEVICE_FEASIBILITY

Blinding Strategy

NONE

Study Groups

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Visual and Auditory Breathing-swallowing Coordinated Training device

Group Type OTHER

Visual and Auditory Breathing-swallowing Coordinated Training device

Intervention Type DEVICE

This device has a structure in which a band wrapped around the chest detects the respiratory phase from changes in the lung volume, and the connected device lights a signal and sounds a sound.

Interventions

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Visual and Auditory Breathing-swallowing Coordinated Training device

This device has a structure in which a band wrapped around the chest detects the respiratory phase from changes in the lung volume, and the connected device lights a signal and sounds a sound.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Subjects with written informed consent to participate in the study

Exclusion Criteria

* Subjects with an apparent swallowing disorder
* Subjects with clinically evident cerebrovascular diseases
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Hospital Organization Minami Kyoto Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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National Hospital Organization Minami Kyoto Hospital

Jōyō, Kyoto, Japan

Site Status

Countries

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Japan

Other Identifiers

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2020-20

Identifier Type: -

Identifier Source: org_study_id

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