Patients With and Without Phonotrauma
Defining Clinically Important Differences in Cepstral and Spectral Measures in Individuals With and Without Phonotrauma
University of Texas Southwestern Medical Center
100 participants
Jan 17, 2023
OBSERVATIONAL
Conditions
Summary
There is a substantial need to identify objective measures associated with hyperadduction of the vocal folds to recognize those at higher risk of developing phonotrauma so that risk mitigation strategies can be implemented before phonotrauma develops. The overall objective of this proposed project is to investigate the sensitivity and direction of change in cepstral peak prominence (CPP) and the magnitude difference between the first two harmonics of the voice spectrum (H1-H2) in response to varied phonation patterns, which will be addressed using the following two aims: Aim 1: Determine how CPP and H1-H2 change as a function of using pressed voice production in individuals without laryngeal pathology. Aim 2: Examine the sensitivity (minimally detectable change) and responsiveness (minimal clinically important difference) of CPP and H1-H2 to detect changes in different voice production conditions.
Eligibility
Inclusion Criteria6
- Control Group:
- 18-65 years of age (to avoid confounding physiological factors related to puberty or presbyphonia)
- No history of or current voice disorder
- Auditory perceptual presentation globally within functional limits (as determined by a voice specialized SLP).
- Diagnosed with phonotrauma (i.e., vocal fold nodules, vocal fold polyp, vocal fold pseudocyst, mid-fold edema) by a laryngologist.
- 18-65 years of age
Exclusion Criteria5
- Atypical auditory-perceptual voice presentation
- History of voice disorder or laryngeal surgery.
- Patient Group:
- Diagnosis of voice disorder not related to phonotrauma (e.g., vocal fold immobility, laryngeal dystonia, primary muscle tension dysphonia, etc.)
- Previous history of laryngeal surgery or voice therapy (to avoid confounding effects of previous treatment).
Interested in this trial?
Get notified about updates and connect with the research team.
Interventions
Acoustic recordings will involve the five repetitions of three vowels (/ɑ, i, u/) and a standard reading passage (Rainbow Passage) in different voice conditions. Control participants will produce voice in breathy, typical, and pressed conditions. Patient participants will produce voice in typical production and in a resonant voice production. High-speed videoendoscopy and simultaneous acoustic recording will occur on one repetition of a sustained /i/ in each requested condition. Data will be collected using a head-mounted microphone.
High-speed videoendoscopy will occur on one repetition of a sustained /i/ in each requested condition. Exams will be recorded using the Phantom V311 high-speed camera (Vision Research, Wayne, NJ) connected to a Storz 70° rigid laryngoscope using a 400 Watt Xenon light source (Titan 400E).
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT05625191