Dysphagia Study Using Novel Microphone Device

This study is looking for people aged 40 to 85 who have difficulty swallowing (dysphagia) due to a stroke. Researchers are testing a new, non-invasive microphone device, which is a thin film patch, designed to be worn on your chin or between your thyroid and cricoid cartilages. This device collects sounds made while you swallow during a routine videofluoroscopic swallow study (VFSS), which is a special X-ray to watch you swallow. The goal is to use this sound data and machine learning to better understand patterns of abnormal swallowing. The main thing they'll be measuring is the normalized surface acoustic swallowing signal up to 30 minutes after the device is used.

Study design
This is an interventional study with a planned enrollment of 50 participants. It is a prospective cohort study, meaning participants are followed forward in time.
What's involved
You would have the investigational nanomembrane patch placed and calibrated during your scheduled barium swallowing test. Medical and demographic information will also be collected.
Compensation
Not stated in the trial record.
Follow-up
The primary measurement will be taken up to 30 minutes post-intervention.

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NCT07251140

Dysphagia Study Using Novel Microphone Device

Recruiting
NAAges 40–85InterventionalBasic science
Emory University
~50 participants
Updated 2025-11-26 on ClinicalTrials.gov
What's tested:Microphone device

At a glance

Recruiting sites
2 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Normalized Surface Acoustic Swallowing Signal
Measured over Up to 30 min post-intervention
Dysphagia
Stroke
2 sites across 1 states
Georgia2
  • Hyojung Choo, PhD · PRINCIPAL_INVESTIGATOR · Emory University

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Eligibility criteria

Inclusion

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.

Exclusion

Head and neck cancer treatment history
  • Normalized Surface Acoustic Swallowing SignalUp to 30 min post-intervention

    Surface acoustic swallowing signals will be collected using a wearable biopatch containing a microphone, placed on study participants. Raw acoustic data will be recorded in voltage and subsequently normalized against background acoustic levels, resulting in a unitless measure expressed in arbitrary units (a.u.).