Individual Differences in Diabetes Risk: Role of Slow WaveSleep
This study has been completed.
Sponsor:
University of Chicago
Information provided by:
University of Chicago
ClinicalTrials.gov Identifier:
NCT00989378
First received: October 1, 2009
Last updated: January 27, 2011
Last verified: January 2011
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Purpose
This study will examine the relationship between the amount of slow wave sleep (deep sleep) and the ability of the body to bring the blood sugar level to a normal range after receiving glucose.
| Condition | Intervention |
|---|---|
|
Sleep Diabetes |
Behavioral: baseline study |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort |
| Official Title: | Ancillary Studies to Major Ongoing NIDDK Clinical Research Studies |
Resource links provided by NLM:
Further study details as provided by University of Chicago:
Biospecimen Retention: Samples Without DNA
serum
| Estimated Enrollment: | 12 |
| Study Start Date: | November 2008 |
| Study Completion Date: | September 2010 |
| Primary Completion Date: | September 2010 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
control
normal healthy men and women
|
Behavioral: baseline study
normal bedtimes
|
Eligibility| Ages Eligible for Study: | 18 Years to 20 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Study Population
normal healthy men and women
Criteria
Inclusion Criteria:
- healthy volunteers age 18-20 with a BMI < 27kg/m2 in women and < 28 kg/m2 in men with normal findings on clinical examination, routine laboratory tests and EKG
- only subjects who have regular life styles (no shift work, no travel across time zone during the previous 4 weeks)
- habitual bedtimes between 7.0-8.5 hours/night
- do not take medications will be recruited
Exclusion Criteria:
- women taking hormonal contraceptive therapy and pregnant women will be excluded
- individuals with a history of psychiatric, endocrine, cardiac or sleep disorders will be excluded
- other exclusion criteria will be: tobacco use, habitual alcohol use of more than 1 drink per day, excessive caffeine intake of more than 300 mg per day
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00989378
Locations
| United States, Illinois | |
| University of Chicago | |
| Chicago, Illinois, United States, 60637 | |
Sponsors and Collaborators
University of Chicago
Investigators
| Principal Investigator: | Eve Van Cauter, Ph.D. | University of Chicago |
More Information
No publications provided
| Responsible Party: | Eve Van Cauter, PhD, Professor, The University of Chicago |
| ClinicalTrials.gov Identifier: | NCT00989378 History of Changes |
| Other Study ID Numbers: | 16026A |
| Study First Received: | October 1, 2009 |
| Last Updated: | January 27, 2011 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by University of Chicago:
|
sleep insulin diabetes determine association between sleep characteristics and diabetes risk |
Additional relevant MeSH terms:
|
Diabetes Mellitus Glucose Metabolism Disorders Metabolic Diseases Endocrine System Diseases |
ClinicalTrials.gov processed this record on May 16, 2013