Mechanisms of Air-pulse Pharyngeal Sensory Stimulation Regulation Post-stroke Swallowing Neural Network Remodeling Via TRPV4 Channel

ConditionDysphagia
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-76
SponsorFirst People's Hospital of Foshan

About this trial

This randomized, double-blind, sham-controlled clinical trial will investigate the effects and potential neural mechanisms of pharyngeal air-pulse sensory stimulation in patients with post-stroke dysphagia. A total of 80 participants with swallowing impairment after stroke will be randomly assigned in a 1:1 ratio to either an active stimulation group or a sham stimulation group. Both groups will receive conventional swallowing rehabilitation, while the active group will additionally receive pharyngeal air-pulse sensory stimulation and the control group will receive sham stimulation for 2 weeks.

Swallowing function and neurophysiological changes will be assessed before and after the intervention. Assessments will include clinical swallowing evaluations, videofluoroscopic swallowing study, surface electromyography, resting-state and task-based functional magnetic resonance imaging, and diffusion kurtosis imaging. The study aims to determine whether pharyngeal air-pulse sensory stimulation can improve swallowing function and to explore associated changes in swallowing-related sensory-motor brain networks after stroke.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Diagnosis of stroke according to the Chinese Guidelines for the Prevention and Treatment of Cerebrovascular Diseases.

Dysphagia confirmed by videofluoroscopic swallowing study (VFSS) or fiberoptic endoscopic evaluation of swallowing (FEES).

Functional Oral Intake Scale (FOIS) score of 1-5.

Stable vital signs.

Disqualifiers

Other neurological or mental system disorders

Severe sensory impairment.

Severe cardiac, pulmonary, hepatic, or renal disease.

History of seizures after stroke.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Air-Pulse Sensory Stimulation

    Device

    Active pharyngeal air-pulse sensory stimulation is delivered using a pharyngeal air-pulse sensory stimulation device. The stimulation site is the anterior wall of the piriform sinus or the aryepiglottic fold. Air-pulse stimulation is delivered at a frequency of 48 pulses per minute, with 1 minute of stimulation alternating with 1 minute of rest, for a total session duration of 20 minutes and approximately 480 air pulses per session.

  • sham intervention

    Device

    Sham pharyngeal air-pulse sensory stimulation is delivered using the same device. The catheter insertion procedure, placement method, and duration are kept consistent with those used in the active stimulation group to maintain blinding.

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: Active Pharyngeal Air-Pulse Sensory StimulationExperimental treatment 1 intervention
Group B: Sham Pharyngeal Air-Pulse Sensory StimulationSham comparator 1 intervention

Trial outcomes

Primary outcomes

1

The Functional Oral Intake Scale (FOIS)

The Functional Oral Intake Scale (FOIS) is a 7-point ordinal scale used to assess the functional level of oral food and liquid intake. Scores range from 1 (nothing by mouth) to 7 (total oral diet with no restrictions). Higher scores indicate better funct

Time frame
Baseline and immediately after completion of the 2-week intervention

Secondary outcomes

1

Penetration-Aspiration Scale (PAS) Score

The Penetration-Aspiration Scale (PAS) is an 8-point ordinal scale used to assess the severity of airway invasion during swallowing. Scores range from 1 to 8, with a score of 1 indicating that material does not enter the airway and a score of 8 indicating that material passes below the vocal folds with no attempt to eject it. Higher scores indicate greater severity of penetration or aspiration.

Time frame
Baseline and immediately after completion of the 2-week intervention
2

Dysphagia Outcome and Severity Scale (DOSS) Score

The Dysphagia Outcome and Severity Scale (DOSS) is a 7-point ordinal scale used to assess the functional severity of dysphagia and the level of dietary restriction and assistance required. Scores range from 1 to 7, with a score of 1 indicating severe dysphagia with inability to safely tolerate oral intake and a score of 7 indicating normal swallowing with a regular diet and no need for compensatory strategies or additional time. Higher scores indicate better swallowing function and lower severity of dysphagia.

Time frame
Baseline and immediately after completion of the 2-week intervention

Other outcomes

1

Oral Transit Time (OTT)

Oral Transit Time (OTT) will be measured from videofluoroscopic swallowing study (VFSS) recordings and expressed in seconds (s). OTT is defined as the time interval from the initiation of posterior oral bolus propulsion until the leading edge of the bolus reaches the ramus of the mandible. Measurements will be obtained using predefined bolus consistencies and volumes.

Time frame
Baseline and immediately after completion of the 2-week intervention
2

Upper Esophageal Sphincter Opening (UO)

Upper Esophageal Sphincter Opening (UO) will be measured from videofluoroscopic swallowing study (VFSS) recordings and expressed in millimeters (mm). UO is defined as the maximum opening diameter of the upper esophageal sphincter during bolus passage, measured on the lateral VFSS image at the point of maximal opening.

Time frame
Baseline and immediately after completion of the 2-week intervention
3

Hyoid Superior Movement (HSM)

Hyoid Superior Movement (HSM) will be measured from videofluoroscopic swallowing study (VFSS) recordings and expressed in millimeters (mm). HSM represents the maximum superior displacement of the hyoid bone from its resting position during swallowing.

Time frame
Baseline and immediately after completion of the 2-week intervention
4

Hyoid Anterior Movement (HAM)

Hyoid Anterior Movement (HAM) will be measured from videofluoroscopic swallowing study (VFSS) recordings and expressed in millimeters (mm). HAM represents the maximum anterior displacement of the hyoid bone from its resting position during swallowing.

Time frame
Baseline and immediately after completion of the 2-week intervention

Locations

This trial has no locations.

Sponsors and contacts

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