None listed
Conditions
Interventions
A thoracic antisupine device with novel design features will be worn during sleep. At the end of one month a home-based overnight sleep study with the device in situ will be performed. After a one week washout, followed by a month on nCPAP the study will be repeated.
Sponsors
University of Otago
Study design
Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Blinded (masking used)
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Adults with positional obstructive sleep apnoea (OSA) with at least 10% of sleep in supine and apnoea hypopnoea index (AHI) twice as much in supine and non supine.
Exclusion criteria
Other co-morbidities interefering with sleep.
Outcome results
None listed