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Expiratory Muscle Strength Training + Voice Therapy for Vocal Cord Paralysis

N/A
Waitlist Available
Led By Adam T Lloyd, SLP-D, MM, MA
Research Sponsored by University of Miami
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Adequate cognition evidenced by score of 24 or higher on the Mini-Mental State Examination (MMSE) survey to determine if the subject has the mental capacity to participate in therapy
Completed voice combination evaluation with speech pathologists and otolaryngologist
Must not have
Non English or Spanish speakers
Individuals with uncontrolled blood pressure
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 16 weeks
Awards & highlights

Summary

This trial tests if adding breathing muscle exercises to regular voice therapy helps people with voice problems due to vocal cords not closing properly. The goal is to see if it improves their breath control, speaking ability, and overall voice quality.

Who is the study for?
This trial is for adults over 18 with glottal insufficiency, who've seen a speech pathologist and otolaryngologist. They must score at least 24 on the MMSE, showing they can follow therapy instructions. It's not for those unable to consent, non-English/Spanish speakers, pregnant women, prisoners, or people with certain medical conditions like uncontrolled blood pressure or chronic respiratory diseases.
What is being tested?
The study tests if adding expiratory muscle strength training (EMST) to standard voice therapy improves breathing strength and voice quality in individuals with vocal cord issues. The goal is to see better maximal expiratory pressure and voice measures such as loudness and duration of sound.
What are the potential side effects?
Potential side effects from EMST may include discomfort while using the device or fatigue due to the exercises. Standard voice therapy generally has minimal risks but could also cause temporary vocal strain or fatigue.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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My mental ability to participate in therapy is confirmed by a test score.
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I have completed a voice check with speech and throat specialists.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I do not speak English or Spanish.
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My blood pressure is not under control.
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I do not have severe, unmanaged lung conditions like COPD.
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I am unable to give consent for medical procedures.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~16 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 16 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Amplitude
Maximum expiratory pressure
Secondary study objectives
Cepstral Peak Prominence (CPP)
Cepstral spectral index of dysphonia (CSID)
Dynamic pitch range
+4 more

Trial Design

3Treatment groups
Experimental Treatment
Group I: Unilateral vocal fold paralysis standard of care voice therapyExperimental Treatment1 Intervention
The participants will receive the standard of voice therapy including improved breath coordination, sustained humming and vowels, vocal glides, resonant voice therapy, and relations techniques.
Group II: Unilateral paralysis standard of care voice therapy plus EMSTExperimental Treatment2 Interventions
The participants will receive the standard of voice therapy including improved breath coordination, sustained humming and vowels, vocal glides, resonant voice therapy, and relations techniques. EMST consists of blowing into respiratory device at a measure threshold pressure. As strength improves threshold resistance will be increased.
Group III: Parkinson's disease standard of care voice therapy plus EMSTExperimental Treatment2 Interventions
The participants will receive the standard of voice therapy including improved breath coordination, sustained humming and vowels, vocal glides, resonant voice therapy, and relations techniques. EMST consists of blowing into respiratory device at a measure threshold pressure. As strength improves threshold resistance will be increased.

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Expiratory Muscle Strength Training (EMST) strengthens the expiratory muscles to enhance respiratory support for phonation, which is crucial for improving voice quality in hoarseness patients. This approach directly addresses muscle weakness that can impair vocal function. Other treatments, such as visual EMG biofeedback and manual circumlaryngeal therapy, reduce laryngeal muscle tension and improve muscle coordination, further enhancing voice quality. These non-surgical therapies are vital for managing hoarseness, offering patients improved communication abilities and quality of life.
EMG biofeedback treatment of pediatric hyperfunctional dysphonia.The Immediate Impact of Targeted Exercises on Voice Characteristics in Female Speakers With Phonotraumatic Vocal Fold Lesions.Effectiveness of voice therapy in patients with vocal fold nodules: a systematic search and narrative review.

Find a Location

Who is running the clinical trial?

University of MiamiLead Sponsor
935 Previous Clinical Trials
422,097 Total Patients Enrolled
Adam T Lloyd, SLP-D, MM, MAPrincipal InvestigatorUniversity of Miami

Media Library

Standard of Care Voice Therapy Clinical Trial Eligibility Overview. Trial Name: NCT03692494 — N/A
Hoarseness Research Study Groups: Unilateral paralysis standard of care voice therapy plus EMST, Unilateral vocal fold paralysis standard of care voice therapy, Parkinson's disease standard of care voice therapy plus EMST
Hoarseness Clinical Trial 2023: Standard of Care Voice Therapy Highlights & Side Effects. Trial Name: NCT03692494 — N/A
Standard of Care Voice Therapy 2023 Treatment Timeline for Medical Study. Trial Name: NCT03692494 — N/A
~80 spots leftby Jun 2026