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Diaphragmatic Function in Stroke Patients.

Diaphragm Function Evaluation in Stroke Patients During Voluntary Cough Using Sonography

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01637649
Enrollment
75
Registered
2012-07-11
Start date
2012-06-30
Completion date
2013-06-30
Last updated
2013-06-19

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

Conditions

Cough, Paralytic Stroke

Keywords

dysphagia,diaphragm, ultrasonography, inspiration, expiration,

Brief summary

* This study attempts to elucidate whether stroke patients with dysphagia have reduced diaphragm movement during voluntary coughing, and also during deep inspiration and expiration than stroke patients without dysphagia. * This study will also compare various spirometric measurements with the diaphragmatic motions.

Detailed description

Stroke is a debilitating condition that can impair multiple functions, including swallowing. Stroke patients with dysphagia, are known to have reduced cough due to multiple mechanisms and this can impair their expectorate function. This can lead to accumulation of sputum and mucoid, ultimately resulting in aspiration pneumonia. Stroke patients, especially those with dysphagia, are also known to have expiratory muscle weakness and weak cough than healthy controls. Stroke patients are also known to have reduced diaphragm movement than healthy subjects. Sonography is a useful tool that can easily and reliability measure diaphragm movement. Whether stroke patients with dysphagia have reduced diaphragm movement than those without dysphagia and whether this affects voluntary cough have not been reported yet. This study attempts to evaluate diaphragm movements during voluntary cough in stroke patients with dysphagia and determine whether this reduced diaphragm movement correlates to their peak flow meters during voluntary cough.

Interventions

None listed

Sponsors

The Catholic University of Korea
Lead SponsorOTHER

Study design

Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Stroke patients with confirmed unilateral brain lesion * Gross aspiration confirmed via FEES or VFSS that would require non oral feeding for group 1. * No gross evidence of dysphagia that would require non oral feeding for group 2. * No prior episode of stroke or dysphagia for the healthy control group.

Exclusion criteria

* Episode of acute pneumonia or pulmonary embolism at time of enrollment * Previous history of chronic respiratory disorders or other systemic disorders that may affect respiratory function ( ex, rheumatoid arthritis, chronic renal disease, spinal cord injury) * Stroke patients with multiple brain lesions * Episode of Diaphragm weakness due to peripheral polyneuropathy or unilateral phrenic nerve palsy * Previous episode of abdominal or thoracic surgery within one year of enrollment * Concomitant diagnosis of myopathy, muscular dystrophy or other disorders that may affect respiratory muscles. * Episode of rib fracture within one year of enrollment * Chronic alcoholism * Patient with previous diagnosis of dementia or with impaired cognitive function that may limit full participation at the evaluation.

Design outcomes

Primary

MeasureTime frameDescription
Diaphragm movement during coughing1 dayDiaphragm movement during voluntary coughing will be recorded by musculoskeletal sonogrpahy

Secondary

MeasureTime frameDescription
Pulmonary Function test1 dayFVC, FEV1, FEF 25-75%, FVC/FEV1 ( % ), Peak cough flow
Motricity indexBaseline
Maximal inspiratory and expiratory pressure1 dayrespiratory pressure meter would be used to measure inspiratory and expiratory strength
Diaphragm movement during inspiration1 dayDiaphragm movement will be recorded after deep inspiration
Diaphragm movement during expiration1 dayDiaphragm movement during expiration will be recorded
Canadian Neurological Stroke ScaleBaseline

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026