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OpenTrials
Completed

NCT Number: NCT00965783

Predictors of the Metabolic Effect of Sleep Loss

To test whether baseline levels of slow wave activity (SWA) during sleep are lower in obese adults, and even lower in persons with sleep disordered breathing (SDB) compared to lean adults.

To compare levels of SWA in individuals in relation to their sleep time, blood pressure, heart rate, and markers of glucose metabolism.

Completed

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Key information

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • healthy,
  • normal sleepers,
  • lean, overweight,
  • obese,
  • pre menopausal

Exclusion criteria

  • no shift workers or night-shift workers,
  • no mental health disorders,
  • no acute or chronic health conditions (stable, well controlled hypertension are accepted),
  • no hormonal treatments,
  • no substances that may interfere with sleep,
  • problems with sleep

Treatment and study plan

Restriction

Other

Time in bed for each subject is restricted by two hours per night for 4 nights

Extension

Other

Bedtime is extended by 2 hours per night for 4 nights

Primary outcomes

  1. Correlation between SWA, sleep duration,sleep architecture, and biomarkers of the metabolic syndrome in lean, obese with and without obstructive sleep apnea.

    Time frame: study completion

Sponsors and collaborators

Lead sponsor

University of Chicago

Other

Registry information

Acronym: SDBO

Important dates

Study start
2007
Primary completion
2009
Study completion
2009
First posted
Aug 26, 2009
Registry last updated
Sep 5, 2013

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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