Reference Values for Videofluoroscopic Measures of Swallowing (NIA_RV)
Dysphagia, Oropharyngeal
About this trial
This is an interventional basic science trial for Dysphagia, Oropharyngeal focused on measuring Deglutition
Eligibility Criteria
Inclusion Criteria:
- Healthy Volunteers: no history of swallowing difficulties.
- Clinical cohorts: physician confirmed diagnosis of the condition of interest plus symptoms of swallowing difficult, defined as a score >/=200 on the Sydney Swallow Questionnaire.
Exclusion Criteria:
- cognitive communication difficulties that may hinder comprehension of the study documents
- known allergies to latex, due to the possibility that these items will come into contact with the oral mucosa during data collection
- current pregnancy
Sites / Locations
- University of Florida
- McMaster University
- University Health Network
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Other
Other
Other
Other
Other
Healthy adults
Parkinson Disease
Chronic Obstructive Pulmonary Disease
Post-ICU
Cardiac Surgery
Adults aged 18 or older with no history of swallowing impairment
Adults with a neurologist-confirmed diagnosis of Parkinson Disease who also report symptoms of swallowing impairment, defined as a score >/= 200 on the Sydney Swallow Questionnaire.
Adults with a respirologist-confirmed diagnosis of Chronic Obstructive Pulmonary Disease who also report symptoms of swallowing impairment, defined as a score >/= 200 on the Sydney Swallow Questionnaire.
Adults who have been hospitalized in the past 3 months and have required intensive care including mechanical ventilation for at least 48 hours. Inclusion in this cohort also requires symptoms of swallowing impairment, defined as a score >/= 200 on the Sydney Swallow Questionnaire.
Adults who have undergone cardiovascular or cardiothoracic surgery in the past 6 months. Inclusion in this cohort also requires symptoms of swallowing impairment, defined as a score >/= 200 on the Sydney Swallow Questionnaire.