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Clinical Trials/NCT05098808
NCT05098808
Completed
Not Applicable

Classification of Dysphagia Patients at Risk of Aspiration Pneumonia Using Machine Learning Algorithms Incorporating Acoustic Features From Phonetic Evaluation

The Catholic University of Korea1 site in 1 country449 target enrollmentSeptember 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Respiration Disorders
Sponsor
The Catholic University of Korea
Enrollment
449
Locations
1
Primary Endpoint
Functional Oral Intake Scale
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

In this prospective study we extracted acoustic parameters using PRAAT from patient's attempt to phonate during the clinical evaluation using a digital smart device. From these parameters we attempted (1) to define which of the PRAAT acoustic features best help to discriminate patients with dysphagia (2) to develop algorithms using sophisticated ML techniques that best classify those i) with dysphagia and those ii ) at high risk of respiratory complications due to poor cough force.

Detailed Description

This study was prospective study, and patients who visited the department of rehabilitation medicine in a single university-affiliated tertiary hospital with dysphagic symptoms from September 2019 to March 2021 were included.Voice recording was performed at the enrollment with blinded assessment, where the participants first visited the rehabilitation department with chief complaints of dysphagia. The cough sounds were recorded with an iPad (Apple, Cupertino, CA, USA) through an embedded microphone. From the acoustic files we extracted fourteen voice parameters that include the average value and standard deviation of the fundamental frequency (f0), harmonic-to-noise ratio (HNR), the jitter that refers to frequency instability, and the shimmer that represents the amplitude instability of the sound signal. Machine learning algorithms and sophisticated deep neural network analysis will be performed.

Registry
clinicaltrials.gov
Start Date
September 1, 2019
End Date
October 1, 2021
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sun Im

associate professor

The Catholic University of Korea

Eligibility Criteria

Inclusion Criteria

  • Inclusion criteria
  • Suspected swallowing disorder who were referred for swallowing assessment
  • Dysphagia attributable to brain lesion including stroke

Exclusion Criteria

  • Participants who were unable to perform phonation
  • Participants who had no VFSS or standardized swallowing assessment results
  • Participants with no spirometric measurements

Outcomes

Primary Outcomes

Functional Oral Intake Scale

Time Frame: during the intervention

Dysphagia severity as measured by the the Functional Oral Intake Scale obtained from standardized swallowing tests

Cough strength

Time Frame: during the intervention

Spirometry values : cough strength as measured by the spirometric values during voluntary cough

Study Sites (1)

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