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Efficacy of swallowing measurement device

Not Applicable
Conditions
Patients with dysphagia
dysphagia
Registration Number
JPRN-jRCTs042180013
Lead Sponsor
Saitoh Eiichi
Brief Summary

The elastic sensors of the device were stretched as the larynx was elevated and descended during the swallowing, and the waveforms of each channel were shown to change in mountainous and valley shapes following the laryngeal movement. The timing when the thyroid cartilage prominence passed through the channel coincided with the timing when the elastic sensor in that channel was stretched the most. The automatic measurement of the number of swallows by the elastic sensor showed good sensitivity and accuracy.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
105
Inclusion Criteria

Subjects who met all the following criteria
Healthy:
1.No history of stroke, neuromuscular diseases, or heart disease
2.Twenty years of age or more
3.Perceived informed consent of this study
Patients:
1.Dysphagia patients who are inpatient or outpatient of Department of Rehabilitation at Fujita Helath University Hospital
2.Medically stable
3.Twenty years of age or more
4.Perceived informed consent of this study

Exclusion Criteria

Subjects who are applicable to the following criteria
Healthy:
History of swallowing difficulty, stroke, neuromuscular diseases, organic dysfunction of larynx and pharynx, respiratory diseases, upper digestive diseases
Patients:
1.Medically instable
2.Who cannot do voluntary movement due to impaired consciousness
3.Who cannot follow the command of therapists

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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