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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00915707
Other study ID # 14916B
Secondary ID
Status Completed
Phase N/A
First received June 3, 2009
Last updated September 4, 2013
Start date January 2007
Est. completion date July 2012

Study information

Verified date September 2013
Source University of Chicago
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This study is designed to study the pathways through which short sleep duration or poor sleep quality can lead to an increased risk of developing diabetes and obesity.


Recruitment information / eligibility

Status Completed
Enrollment 23
Est. completion date July 2012
Est. primary completion date July 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- Normal weight

- Healthy

- Normal sleep times

Exclusion Criteria:

- Sleep disorders

- Overweight

- Diabetes

- Other health conditions

- Excessive caffeine and alcohol intake

- Smoking

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject)


Related Conditions & MeSH terms


Intervention

Other:
Baseline
Subjects are allowed time in bed for sleep as their usual time at home.
Sleep restriction
Subjects sleep is reduced to 4.5 hours in bed for 4 nights.
Reduced Sleep Quality
Subjects sleep quality is reduced for 4 nights.

Locations

Country Name City State
United States The University of Chicago Chicago Illinois

Sponsors (1)

Lead Sponsor Collaborator
University of Chicago

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Disposition Index reflecting Diabetes Risk as a result of decreased sleep duration and/or quality. 3 months No
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