Metabolic Syndrome Clinical Trial
— RehsolvasOfficial title:
Effects of an In-Patient Individualized Rehabilitation Program on Severity and Symptoms of Obstructive Sleep Apnea Syndrome (OSAS):Results of a Randomized Controlled Pilot Study
The obstructive sleep apnea/hypopnea syndrome (OSAS) is a common disease (2-4% of the
general population) that generates intermittent hypoxemia and sleep fragmentation. OSAS is
associated with various metabolic disorders such as metabolic syndrome, type 2 diabetes.
OSAS is a risk factor for cardio-vascular diseases by increasing morbidity/mortality. OSAS
patients suffer from excessive daytime sleepiness (EDS), a symptom also responsible for at
least 30% of traffic accidents but also other cognitive disorders with significant impact on
quality of life. OSAS generates oxidative stress, inflammation and resistance to insulin and
other systemic metabolic dysregulation of many whose levels are correlated with the severity
of the disease.
Treatment with Continuous Positive Airway Pressure (CPAP) has clearly demonstrated its
effectiveness to eliminate apneas and improve EDS but it is sometimes difficult to accept
and/or poorly tolerated, limiting its effectiveness.
Weight loss and regular physical activity are clearly recommended but rarely done in
clinical practice. A few studies have applied to study the effects of rehabilitation
training (REE) on the sleep apnea patients and have shown an improvement in sleep quality,
reduction of awakenings and arousals from sleep and the Index of Apnea/Hypopnea (AHI), but
their methodology was questionable, and the number of patients included was too low.
The investigators hypothesis is that an in-patient multidisciplinary rehabilitation program
comprising educational activities, dietary management and individualized exercise training
(IET) will decrease OSAS severity, improve sleep quality and symptoms (EDS, fatigue, QoL).
This IET program (24 sessions during 4 weeks) could also help to improve many metabolic
dysregulation, inflammation and oxidative stress (also markers of cardiovascular risk).
Leptin, a hormone involved in regulating appetite, energy expenditure and ventilatory
control is increased in OSA (mechanism of leptin resistance). The improved sensitivity to
leptin may play a role in enabling a better control of ventilation in these patients.
Status | Completed |
Enrollment | 26 |
Est. completion date | August 2010 |
Est. primary completion date | June 2010 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 30 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Moderate to severe Obstructive Sleep Apnea Hypopnea Syndrome (AHI > 15/h) - Sedentary patient (Activity Voorrips Questionnary score < 9,4) Exclusion Criteria: - OSAS already treated by CPAP or other therapy (OAM,...) - BMI > 40/m² - Hypnotic and sedative medications - Cranio-facial malformation - Obstructive respiratory disease (COPD, asthma,...) - Instable heart ischemic disease and all |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
France | Clinique du souffle "La Solane" | Osseja |
Lead Sponsor | Collaborator |
---|---|
5 Santé | A.E.R.O.B.I.E., INSERM U1046 Physiologie et médecine expérimentale du cœur et des muscles |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Delta of the Apnea/Hypopnea Index (AHI)between the two arms | Comparing Delta of AHI 4 weeks (J0/J28) after starting the intervention (assessed by polysomnography at inclusion - end monitoring) between the two arms using the Student t test or Wilcoxon test if the distribution is not Gaussian. | participants will be followed for the duration of hospital stay, an expected average of 4 weeks | Yes |
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