RecruitingNot ApplicableNCT05273190
Stimulation of the Larynx to Treat Unexplained Chronic Cough
Vibrotactile Stimulation of the Larynx to Treat Unexplained Chronic Cough
Sponsor
University of Minnesota
Enrollment
60 participants
Start Date
Jul 13, 2021
Study Type
INTERVENTIONAL
Conditions
Summary
Researchers will test the effect of non-invasive vibrotactile stimulation of the larynx on symptom severity of unexplained chronic cough.
Eligibility
Min Age: 18 YearsMax Age: 88 Years
Inclusion Criteria5
- Adults aged 18-88
- \>8 weeks of cough
- Cough visual analogue scale (VAS): Rating of 30 or greater on a 0-100 cough severity scale
- Ability to provide informed consent and independently complete questionnaires
- Ability to read and speak English
Exclusion Criteria13
- Electronic implants (e.g., pacemaker)
- Currently doing speech therapy for cough
- Contraindications to safe or effective VTS device use
- No regular access to wifi internet Neuromuscular impairment that may affect cough/laryngeal sensation and/or function (e.g., multiple system atrophy, Parkinson, CVA, vocal fold paralysis or paresis)
- Untreated carotid disease
- BMI \> 40 (for transmission of VTS through soft tissue)
- Current or recent (quit \< 3 months ago) smoking
- Known currently infectious cause for cough (e.g., TB, pertussis, COVID)
- History of known or suspected aspiration pneumonia
- Diagnosis or clinical suspicion of chronic obstructive pulmonary disease (COPD)
- Diagnosis or clinical suspicion of interstitial lung disease (ILD)
- Unmanaged reflux
- Unmanaged allergies/postnasal drip
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Interventions
DEVICEVibrotactile Stimulation
Small electric motors, similar to a vibrating cell phone or gaming joystick, deliver vibration to the throat. Participants will assess cough symptoms throughout the study period.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT05273190
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