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Outcomes of Sleep Disorders in Older Men - Article


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Cardiovascular Diseases And Disorders

Cardiovascular Diseases


Clinical Trial: Outcomes of Sleep Disorders in Older Men

This study is no longer recruiting patients.

Sponsored by: National Heart, Lung, and Blood Institute (NHLBI)
Information provided by: National Heart, Lung, and Blood Institute (NHLBI)

Purpose

To determine the effects of sleep disorders on cardiovascular function and disease in older men.

Condition Treatment or Intervention
Cardiovascular Diseases
Heart Diseases
Sleep
Sleep Apnea Syndromes
Neurologic Manifestations
Osteoporosis
Bone Diseases
 Procedure: Polysomnography

MedlinePlus related topics:  Bone Diseases;   Heart Diseases;   Heart Diseases--Prevention;   Neurologic Diseases;   Osteoporosis;   Sleep Apnea;   Vascular Diseases

Study Type: Observational
Study Design: Defined Population

Further Study Details: 

Study start: September 2003;  Study completion: June 2007

BACKGROUND: It is estimated that over 50 percent of adults aged 65 and older report some sleep disruption, while about 20 percent suffer from chronic insomnia. Obstructive sleep apnea, a major cause of daytime drowsiness, occurs in an estimated 20-60 percent of older people, depending on the definition used and the specific population being studied. Despite the high prevalence of sleep disorders in the elderly, there have been relatively few studies focused on the consequences. Most studies have been limited by cross-sectional design, small sample size, or lack of comprehensive and objective assessment of sleep. The study, Outcomes of Sleep Disorders in Older Men, will take advantage of the established cohort that has been recruited for the Osteoporotic Fractures in Men (MrOS) Study (5U01AR045647-Dr. Eric Orwoll, PI). MrOS, a 7-year study that began in July 1999, is a multi-center prospective study of approximately 6,000 men aged 65 and older. During the MrOS baseline visit, a broad variety of measurements were collected, including body composition and body fat distribution by dual energy X-ray absorptiometry (DEXA) and quantitative computed tomography, bone density, anthropometry, performance-based tests of strength and balance, medical history, medication use, smoking and alcohol use, and other parameters. Blood, urine, and DNA specimens have been archived for use in future studies of importance to the health of older men.

DESIGN NARRATIVE: In a subcohort of 3,000 MrOS participants, comprehensive and accurate assessments of sleep will be added using in-home polysomnography, wrist actigraphy, questionnaires and other measures; and prospective adjudication of cardiovascular disease (CVD) events, to the extensive measures that have already been performed or planned in the MrOS cohort study. These new measures will enable testing of several important hypotheses: 1) to characterize the associations between sleep disruption and subsequent CVD events during 3.5 years of follow-up, 2) to determine if sleep disturbances are associated with an increased risk of total and cause-specific mortality in older men, 3) to test whether sleep disturbances are associated with increased risk of falls and decreased physical function, 4) to test whether sleep disturbances are associated with impaired cognitive function in older men, and 5) to test whether sleep disorders are associated with bone density and fracture risk in older men. The bank of MrOS specimens will be supplemented to allow for testing of future hypotheses concerning the role of sleep in the development of age-related diseases and conditions.

Eligibility

Ages Eligible for Study:  65 Years and above,  Genders Eligible for Study:  Male

Criteria

No eligibility criteria

Location Information

Study chairs or principal investigators

Elizabeth Barrett-Connor,  University of California at San Diego   
Jane Cauley,  University of Pittsburgh   
Kristine Ensrud,  University of Minnesota Twin Cities   
Cora Lewis,  University of Alabama, Birmingham   
Eric Orwoll,  Oregon Health & Science University   
Susan Redline,  Case Western Reserve University   
Marcia Stefanick,  Stanford University   
Katie Stone,  University of California, San Francisco   

More Information

Study ID Numbers:  158
Record last reviewed:  December 2004
Last Updated:  January 10, 2005
Record first received:  October 6, 2003
ClinicalTrials.gov Identifier:  NCT00070681
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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Page Updated: September 6, 2005
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