Dysphasia
Conditions
Interventions
Subject will be conducted to swallow attached laryngeal motion monitor on them flont neck.
Measurement items are 4 saliva swallow and 4 liquid swallow (In case of subject with modelate or severe dysph
Sponsors
Otaka Yohei
BANDO Chemical Industries
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. healthy subjects over 20 years old who have no history of stroke, neuromuscular or cardiac diseases and have given informed consent for this study 2. patients with dysphagia aged 20 years or older who are inpatients or outpatients of the Rehabilitation Department of our hospital, are in stable general condition, and have given informed consent for this study.
Exclusion criteria
Exclusion criteria: 1. patients with complaints of dysphagia, stroke, neuromuscular diseases, organic diseases of the larynx and pharynx, respiratory diseases, or upper digestive diseases 2. patients with unstable general condition, patients who are unable to perform voluntary movements due to impaired consciousness, patients who cannot receive instructions from a therapist, and patients whom the principal investigator or subinvestigators deem inappropriate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Laryngeal motion captured during swallowing by a swallowing motion monitor Laryngeal motion during swallowing detected by X-ray fluoroscopy | — |
Secondary
| Measure | Time frame |
|---|---|
| Laryngeal elevation duration during swallowing captured by a swallowing motion monitor Laryngeal elevation duration during swallowing detected by X-ray fluoroscory | — |
Contacts
Public ContactSeiko Shibara
Fujita Health University Hospital
Outcome results
None listed