SLEEP APNEA SYNDROME Clinical Trial
Official title:
Effects of a Comprehensive Management Program for the Treatment of Obstructive Sleep Apnea Syndrome
Study objetives : The aim of this study is to assess the impact of a combined therapy treatment (physical exercise, oropharyngeal exercises and dietary recommendations) on symptoms and quality of life in patients with OSAS, as an alternative or addition to therapeutic treatment with nocturnal CPAP.
The obstructive sleep apnea syndrome (OSAS) is characterized by repetitive obstruction of
the upper airway during sleep. OSAS is associated with a wide range of health consequences
such as daytime sleepiness, cognitive impairment and metabolic and cardiovascular diseases.
In Spain the prevalence of this disease is 3 to 6%, constituting a public health problem.
The recommended first line treatment for OSAS is continuous positive pressure airway (CPAP).
Physical exercise has been shown to ameliorate the consequences of OSAS such as
cardiovascular disease, glucose intolerance and fatigue. Scientific studies have shown that
vigorous physical activity is associated with a decrease in the prevalence of OSAS, improved
sleep efficiency and the Epworth Sleepiness Scale.
Moreover, recent evidence has shown that oropharyngeal exercises can be useful in the
treatment of OSAS decreasing neck circumference, snoring, subjective sleepiness and AHI as
well as improving the quality of life and saturation oxygen.
The 60-70% of patients with OSAS is overweight or obese showing that a high body mass index
(BMI) is an independent risk factor for the occurrence of OSAS. Many studies have shown that
weight loss is associated with significant reduction in AHI.
However, despite the scientific evidence to justify the inclusion of these modalities, there
is no study that has analyzed the impact of performing together all these interventions. It
is expected that the combination can produce a cumulative effect that impacts significantly
on improving indicators of OSAS.
The investigators will include patients with a recent diagnosis of moderate or severe OSA.
Patients will be randomized to interventional or control group.
Patients included in the study will be followed for almost three months and they will be
examined at baseline and after time of follow-up or intervention.
;
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
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