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Clinical Trials/NCT00486746
NCT00486746
Unknown
N/A

Lifestyle Intervention Treatment for Patients With Mild Obstructive Sleep Apnea

Kuopio University Hospital1 site in 1 country81 target enrollmentOctober 2004

Overview

Phase
N/A
Intervention
Not specified
Conditions
Obstructive Sleep Apnea
Sponsor
Kuopio University Hospital
Enrollment
81
Locations
1
Primary Endpoint
To evaluate, if weight reduction and lifestyle intervention improve the symptoms of mild obstructive sleep apnoea
Last Updated
6 years ago

Overview

Brief Summary

The main objective of the study is to determine whether a supervised lifestyle intervention including individualized dietary counseling could be a curative treatment for patients with mild OSA.

Detailed Description

Obstructive sleep apnea (OSA) is one of the most common sleep disturbances, and it has been estimated that one out of five adults has at least some degree of sleep related breathing disturbances. Obstructive sleep apnea affects mostly the middle-aged work force, and causes a negative impact on public health by increasing both morbidity and mortality. Obesity is related to many diseases including diabetes, cardiovascular diseases, and metabolic syndrome,and obesity is also considered as the most important risk factor for OSA.Considering the prevalence of mild OSA, and the beneficial effects of even a slight weight loss on both the severity of OSA and the likelihood of developing OSA, lifestyle intervention including weight reduction represents a viable option for the treatment of patients with mild OSA.However, although included in the clinical guidelines, there is a definite lack of well executed studies on the effect of weight reduction upon OSA. Accordingly, we are conducting a randomized study on the effects of lifestyle intervention in the most prevalent subgroup of OSA patients, overweight patients with mild OSA. The study is an on-going prospective, randomized, parallel group trial. The main objective of the study is to determine whether a supervised lifestyle intervention including individualized dietary counseling could be a curative treatment for patients with mild OSA.

Registry
clinicaltrials.gov
Start Date
October 2004
End Date
December 2021
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Kuopio University Hospital
Responsible Party
Principal Investigator
Principal Investigator

Juha Seppa

PhD

Kuopio University Hospital

Eligibility Criteria

Inclusion Criteria

  • Age 18-65 years
  • Apnea-hypopnea index 5-15
  • BMI 28-40

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

To evaluate, if weight reduction and lifestyle intervention improve the symptoms of mild obstructive sleep apnoea

Time Frame: 3 months

To evaluate, if these favourable changes remain in follow-up.

Time Frame: 1, 2 and 5 years

Secondary Outcomes

  • To evaluate, whether the treatment of mild OSA prevents the development of diseases in general associated with sleep apnoea(5 years)
  • To evaluate, whether the mild OSA has detrimental effects on cardiovascular functions and glucose-, insulin- and lipid metabolisms, regulation of autonomous nervous system, endothelial function, baroreflex sensitivity(baseline, 3 months, 1, 2 and 5 years)
  • To evaluate, if improvement of mild OSA has beneficial influence on quality of life, cardiovascular functions and glucose-, insulin- and lipid metabolisms, regulation of autonomous nervous system, endothelial function, and anatomy of the pharynx(1,2,5 years)

Study Sites (1)

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