Single centred, interventional study on abdominal breathing to eliminate/reduce sleep apnoea.
- Conditions
- Sleep Disordered Breathing (SDB)Sleep ApnoeaRespiratory - Sleep apnoea
- Registration Number
- ACTRN12618000694213
- Lead Sponsor
- Dr Peter Keller
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 2000
1. People who have experienced disturbed sleep patterns,
2. People who have been witnessed to have apnoeic episodes,
3. People who have been medically diagnosed with mild/moderate/severe Sleep Disordered Breathing (SDB), on treatment but not compliant partially/fully.
Exclusion criteria will be PPs with pacemaker, implantable cardioverter defibrillator (ICD), on dialysis, pregnancy or lactation, current participation in another clinical trial, medication usage that could influence respiration or sleep (eg, regular use of sedatives, heavy alcohol consumption), OSA with uncontrolled or untreated cardiovascular disease, severe somatic or psychiatric disorders those who were tested positive for narcolepsy/cataplexy, idiopathic somnolence, severe somatic or psychiatric disorders, children and young people, People highly dependent on medical care, people who may be involved in illegal activities, people with cognitive impairment and intellectual disability or a mental illness.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method