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OpenTrials
Active, Not Recruiting

NCT Number: NCT00005557

Epidemiology of Sleep-Disordered Breathing in Adults

To characterize the natural history and biologic spectrum of sleep disordered breathing (SDB) and other sleep problems and disorders, and test hypotheses regarding the causes and consequences of SDB and other sleep problems and disorders.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

About this study

BACKGROUND:

Recent research has shown that sleep disordered breathing (SDB) is much more common than previously thought. While it is known that in clinic samples, SDB is associated with hypertension, cardiovascular disease and mortality, little is known about the natural history of this disorder, particularly in the general population, nor about the causal role of known risk factors. The knowledge obtained from the results of this study will help advance the field of sleep disorders medicine. Information about longitudinal effects and causal relationships may be applied to clinical situations, thus reducing the morbidity and mortality associated with this disorder.

DESIGN NARRATIVE:

In this longitudinal study, follow-up polysomnography and other protocols are conducted on an established cohort of men and women (age 30-60 years at the time of initial recruitment in 1989), currently enrolled in the Wisconsin Sleep Cohort Study. The study aims to : 1) describe the natural history of SDB across middle and older age; 2) investigate associations of SDB with early and intermediate markers of cardiovascular dysfunction, damage, and cardiovascular disease; 3) investigate the longitudinal association of SDB in accelerated cognitive decline; 4) investigate the association of SDB and adverse sleep characteristics with age-related risk factors and outcomes.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Employee of one of the 4 Wisconsin state agencies
  • Age 30-60 in 1988

Exclusion criteria

  • Current pregnancy
  • Unstable or decompensated cardiopulmonary disease
  • Airway cancer
  • Recent upper respiratory surgery

Treatment and study plan

Primary outcomes

  1. sleep disorders and problems, cardiovascular and cognitive outcomes

    Time frame: measured at each study visit

    Overnight polysomnography is used to assess sleep pathology. Questionnaires are used to assess sleep habits. A variety of clinical and laboratory assessments measure cardiovascular and cognitive outcomes.

Secondary outcomes

  1. cardiovascular outcomes

    Time frame: measured at each study visit

    A variety of clinical and laboratory assessments measure cardiovascular outcomes.

Other outcomes

  1. cognitive outcomes

    Time frame: measured at each study visit

    A variety of clinical and laboratory assessments measure cognitive outcomes.

  2. gait and balance

    Time frame: measured at each study visit

    A series of walking tests are conducted.

  3. mental health outcomes

    Time frame: evaluated at each study visit

    Questionnaires assess mood, depression, and anxiety.

Sponsors and collaborators

Lead sponsor

University of Wisconsin, Madison

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

Registry information

Important dates

Study start
1999
Primary completion
2028
Study completion
2031
First posted
May 26, 2000
Registry last updated
Oct 22, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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