Actively Recruiting
The Importance of Positive Expiratory Pressure Associated With the In-exsufflator in ALS Patients
Led by Groupe Hospitalier du Havre · Updated on 2026-01-21
11
Participants Needed
1
Research Sites
114 weeks
Total Duration
On this page
Sponsors
G
Groupe Hospitalier du Havre
Lead Sponsor
F
French Physiotherapy Society / Société Français de Physiothérapie
Collaborating Sponsor
AI-Summary
What this Trial Is About
Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disorder that impairs motor neurons, with a life expectancy of 2 to 7 years after diagnosis. ALS manifests as 'spinal' when it primarily affects limbs, or 'bulbar' when it impairs speech and swallowing. The disease progressively weakens all skeletal muscles, causing respiratory issues and increased risk of lung infections due to ineffective coughing. Mechanical cough assistance via In-exsufflation therapy/ mechanical in-exsufflator devie (INEX/MI-E) applies positive and negative airway pressures non-invasively to improve coughing. However, MI-E may fail in some ALS patients due to airway collapse, often related to brainstem muscle dysfunction.Research by Andersen et al. in 2017 highlighted that during MI-E, ALS patients often experience adverse laryngeal movements, which can obstruct airways and reduce the therapy's effectiveness. To combat this, they suggested individualized MI-E settings to minimize airway collapse. Modern MI-E devices, such as the EOVE-70, offer adjustable positive expiratory pressure (PEP) between cycles to potentially enhance airway stability and coughing efficiency. The current study focuses on the impact of PEP during therapy pauses on the peak expiratory flow rate in ALS patients, which could lead to improved therapeutic outcomes.
CONDITIONS
Official Title
The Importance of Positive Expiratory Pressure Associated With the In-exsufflator in ALS Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female patient aged over 18 years
- Patient diagnosed with Amyotrophic Lateral Sclerosis (ALS)
- Patients with established or beginning bulbar symptoms such as speech impairment, hypersalivation, or swallowing difficulties
- Patient naive to In-exsufflation (INEX) therapy but prescribed for installation or patient already treated with an INEX device
- Patient followed by the ALS mobile team of the Groupe Hospitalier du Havre or the CHU of Dijon
- Disease progression compatible with inclusion as judged by medical team
- Patient willing to participate after receiving adequate information
- Patient covered by social security or a similar scheme
You will not qualify if you...
- Recent respiratory infection episode within the past month
- Mental illness interfering with proper use of the device
- History of laryngospasm
- Inability to attend consultations with the ALS team at the Groupe Hospitalier du Havre or CHU of Dijon
- Pregnancy
- Person deprived of liberty by judicial or administrative decision or under legal protection measures
- Presence of any non-inclusion criterion
- Refusal to participate after inclusion
- Death from any cause
AI-Screening
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Trial Site Locations
Total: 1 location
1
GH Havre
Le Havre, Normandy, France, 76290
Actively Recruiting
Research Team
Y
Yann Combret, PT, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
2
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