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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00716222
Other study ID # B40320084032
Secondary ID
Status Recruiting
Phase N/A
First received July 15, 2008
Last updated January 20, 2009
Start date May 2008
Est. completion date May 2009

Study information

Verified date January 2009
Source Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Contact Veronique VB Beauloye, PhD
Phone +3227641370
Email Veronique.Beauloye@uclouvain.be
Is FDA regulated No
Health authority Belgium: Institutional Review Board
Study type Observational

Clinical Trial Summary

There is a well-documented relationship between short sleep duration and high body mass index (BMI). The mechanism linking short sleep duration and weight gain is unknown. Current studies in healthy young volunteers have shown that experimental sleep restriction is associated with dysregulation of the neuroendocrine control of appetite and with alterations in glucose metabolism. The goal of our study is to determine the metabolic and hormonal modifications induced by chronic sleep curtailment in obese adolescents and young adults and to observe if short sleep is a negative prognostic factor in their weight evolution.


Description:

The main purpose of the study is investigate whether the concentrations of 2 hormones that regulate appetite (leptin, ghrelin), cytokines (TNF-a, IL-6) and CRP are modified in obese adolescents and young adults who had sleep disorders in comparison to obese adolescents and young adults who sleep longer.


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date May 2009
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 13 Years to 25 Years
Eligibility Inclusion Criteria:

- 13-25 years old

- BMI > 30 kg/m2 (If adolescents aged under 18 years: BMI equivalent to a BMI for age and sex to a BMI of 30, according to the Cole et al. obesity criteria).

Exclusion Criteria:

- Infection

- Liver disease

- Chronic inflammatory disease

- Endocrine disease

- Use of drugs that alter the sensitivity of insulin

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Belgium Cliniques Universitaires Saint Luc Brussels

Sponsors (1)

Lead Sponsor Collaborator
Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Country where clinical trial is conducted

Belgium, 

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