Actively Recruiting
Strengthening Inspiratory and Oropharyngeal Muscles in Moderate Obstructive Sleep Apnea Hypopnea Syndrome
Led by Centre Hospitalier Universitaire de Saint Etienne · Updated on 2025-01-29
38
Participants Needed
2
Research Sites
82 weeks
Total Duration
On this page
Sponsors
C
Centre Hospitalier Universitaire de Saint Etienne
Lead Sponsor
A
Association aide à la recherche médicale de proximité (AIRE)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The Obstructive Sleep Apnea hypopnea Syndrome (OSAS), whose prevalence is 4% of the French population, can lead to serious health consequences (risk of road accidents, onset of cardiovascular disease, etc.). OSAS corresponds to a certain number of interruptions (apneas) or reductions (hypopneas) of ventilation during sleep. The weakening of the tone of the inspiratory and oropharyngeal muscles is one of the main causes of upper airways obstruction during the inspiratory phase.
CONDITIONS
Official Title
Strengthening Inspiratory and Oropharyngeal Muscles in Moderate Obstructive Sleep Apnea Hypopnea Syndrome
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Moderate SAHOS (15 3 AHI 3 30)
- Body Mass Index (BMI) < 35
- Patient affiliated or entitled to a social security scheme
- Patient having signed a consent to participate in the study
You will not qualify if you...
- Excessive daytime sleepiness: Epworth sleepiness score > 10
- Professional driving and history of accidents related to sleepiness
- Severe obstructive or restrictive ventilatory disorders of neuromuscular origin authenticated by respiratory function tests
- Patients undergoing treatment for OSAS or requiring immediate initiation of continuous positive airway pressure (CPAP) or a mandibular advancement orthosis
- Patients who have stopped CPAP or orthosis treatment in less than one month
- Patients undergoing cardiorespiratory exercise rehabilitation or starting regular physical training
- Uncompensated heart failure, thoracic sternotomy surgery < 4 months
- Marked osteoporosis with history of rib fractures
- History of spontaneous pneumothorax
- Severe asthma
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
CHU de Grenoble
Grenoble, France, 38000
Not Yet Recruiting
2
Centre Hospitalier Universitaire
Saint-Etienne, France, 42055
Actively Recruiting
Research Team
A
Amandine ZELLAG, physiotherapist
CONTACT
P
Pierre LABEIX, physiotherapist
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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