Novel Acoustic Biopatch for the Investigation of Dysphagia

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study aims to collect swallowing acoustics with a novel non-invasive wearable surface microphone device during routine work-up, videofluoroscopic swallow study (VFSS), of patients with dysphagia (swallowing trouble). The collected microphone data will be analyzed to find the pattern of abnormal swallowing by machine learning algorithm.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Maximum Age: 85
Healthy Volunteers: f
View:

• Diagnosis or suspected stroke

• Stroke with additional neurological disorders

• Age between 40 and 85

• Male and Female

• Scheduled to VFSS due to suspected dysphagia, which is determined by bedside water swallowing test and EAT-10 questionnaire as a standard of care.

Locations
United States
Georgia
Emory University Hospital
RECRUITING
Atlanta
Emory University Hospital Midtown
RECRUITING
Atlanta
Contact Information
Primary
Hyojung Choo, PhD
hyojung.choo@emory.edu
404-727-3727
Time Frame
Start Date: 2025-10-12
Estimated Completion Date: 2026-09-30
Participants
Target number of participants: 50
Treatments
Experimental: Novel Acoustic Biopatch for the Investigation of Dysphagia Cohort
The device is composed of a sensor (disposable part) and a circuit (reusable part).~The device will be applied to the anterior neck of dysphagia symptomatic patients who will be accessed with routine dysphagia investigation, such as standard swallowing evaluation with a modified barium swallow (VFSS). Device will be applied by authorized investigators to specific area to target specific neck muscles where no interference occurs for X-ray imaging (VFSS) interpretation. Acoustic data collected via device will be compared with X-ray imaging (VFSS) to train Convolutional neural network (CNN) algorithm to improve accuracy and to determine accuracy of device.
Related Therapeutic Areas
Sponsors
Leads: Emory University

This content was sourced from clinicaltrials.gov