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Efficacy of swallowing measurement device

Efficacy of swallowing measurement device using elasticity sensor - Efficacy of swallowing measurement device

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs042180013
Enrollment
160
Registered
2018-11-13
Start date
2019-01-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with dysphagia dysphagia

Interventions

Measure the hyolaryngeal elevation during swallowing saliva or liquid

Sponsors

Saitoh Eiichi
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Number of swallows, Duration of hyolaryngeal elevation

Secondary

MeasureTime frame
Number of swallows by visual examination, Number of swallows counted by subject, Time measurement of structures movement

Contacts

Public ContactSeiko Shibata

Fujita Health University Hospital

sshibata@fujita-hu.ac.jp+81-562-93-2167

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026