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Myofunctional Therapy for Obstructive Sleep Apnea

Myofunctional Therapy for Obstructive Sleep Apnea

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07301125
Enrollment
30
Registered
2025-12-24
Start date
2026-10-15
Completion date
2027-09-30
Last updated
2026-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obstructive Sleep Apnea

Keywords

Obstructive Sleep Apnea, Myofunctional Therapy, High-Resolution Manometry

Brief summary

The purpose of this study is to explore a new way to examine the function of the muscles using a technique called high-resolution manometry. The study will enroll 30 adults with OSA, all of whom will use the myofunctional therapy (MFT) devices for 3 months. High-resolution manometry will be used to measure the amount of pressure generated by the muscles of the throat when drinking water or breathing air, both with and without the MFT devices, and before and after the MFT intervention. If successful, this method can help us understand why sleep improves after MFT.

Interventions

The intervention consists of 90 days of MFT (5-6 days/week) along with completing daily logs. MFT will include high-intensity swallowing exercises and respiratory muscle strength training.

Sponsors

University of Minnesota
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Adults aged 18-65 * New diagnosis of OSA (AHI ≥ 5) or failure of first-line OSA treatment * Willingness to forego first-line OSA treatment or stop current OSA treatment for 3 months

Exclusion criteria

* Medical comorbidities that require restricting fluid intake (e.g., dysphagia, renal disease, liver disease, hyponatremia) * Severe nasal obstruction * Severe ankyloglossia * Craniofacial abnormality * Severe pulmonary disease * Severe post-traumatic stress disorder (PCL-5 \> 33) * Very severe insomnia (ISI \> 22) * Body mass index (BMI) ≥30 kg/m2. * History of TBI * Known oropharyngeal or esophageal dysphagia * Pregnancy * Allergy to topical anesthetic * Inability to fast for 6 hours * Recent facial trauma * Recent nasal, pharyngeal, laryngeal, or esophageal surgery * Known nasal, pharyngeal or esophageal obstruction * Current upper respiratory infection * Insufficient internet/computer access to participate in remote study visit * Severe excessive daytime sleepiness (risk of motor vehicle accidents) * Heart failure, recent stroke, heart attack, etc. * Nasal Obstruction Symptom Evaluation (NOSE) Scale \>15

Design outcomes

Primary

MeasureTime frameDescription
MFT treatment fidelityDay 90Treatment fidelity of two common MFTs (high-intensity swallowing exercises, respiratory muscle strength training) in individuals with OSA. Treatment fidelity will be determined via measuring the percent of sessions completed relative to the targeted number of sessions.
Pressure generation in posterior upper airway musculatureDay 90Comparison of pressure generation in posterior upper airway musculature before and after MFT intervention as assessed with HRM

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORJesse Hoffmeister, PhD, CCC-SLP

University of Minnesota

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 17, 2026