1. Obstructive sleep apnoea syndrome (OSAS) 2. Chronic obstructive pulmonary disease (COPD) Respiratory 1. Obstructive sleep apnoea syndrome (OSAS) 2. Chronic obstructive pulmonary disease (COPD)
Conditions
Interventions
Participants attend a total of five study visits. At the first study visit, after provision of informed consent, participants complete a range of spirometry tests. The visit lasts for a total of aroun
Sponsors
Association pour le Développement et l'Organisation de la Recherche en Pneumologie et sur le Sommeil (ADOREPS)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Moderate to severe OSAS diagnosed thanks to polysomnography 2. COPD diagnosed thanks to the symptoms and functionnal respiratory analysis 3. Aged 18 years and over 4. Should understand the informations and sign the consent
Exclusion criteria
Exclusion criteria: 1. Pregnant or nursing women (female patients) 2. Under judicial protection 3. If the subject realises an other study wich prohibits him to be involved in another study 4. Aged under 18 years
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| 1. Angulations in posture is measured using the EOS® system on study visit 3 (as well as 4 and 5 for OSAS patients) 2. Gait velocity is measured using the stand up and go test on study visit 3 (as well as 4 and 5 for OSAS patients) | — |
Primary
| Measure | Time frame |
|---|---|
| Postural stability is assessed using a force platform and motion capture taken by an optoelectronic VICON system on study visit 3 (as well as 4 and 5 for OSAS patients) | — |
Countries
France
Contacts
Public ContactValérie Attali
Outcome results
None listed