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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01964118
Other study ID # 201303081
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 2013
Est. completion date September 2016

Study information

Verified date May 2021
Source Washington University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of Intermittent Fasting study is to investigate whether intermittent fasting could decrease the chronic inflammation levels in overweight/obese people.


Description:

The primary objective of this study is to determine whether or not IF reduces the level of chronic inflammation as evidenced by a decrease in high sensitive C-reactive protein (hsCRP), as the main outcome measure


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date September 2016
Est. primary completion date September 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 30 Years to 65 Years
Eligibility Inclusion Criteria: - The participants in this study will be 50 men and women in the 30 to 65 year age range, who have a BMI in the high normal to moderately obese range (i.e. 24 to 35 kg/m2), - Participants who are eating usual US diets and are sedentary to moderately active (i.e. not exercise trained). Exclusion Criteria: - History of any chronic disease process that could interfere with interpretation of results - Smoking, pregnancy, alcoholism, psychiatric problems, life situations that would interfere with study participation and compliance.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Intermittent Fasting group
Intermittent fasting for 12 months
control group
usual diet for 6 months and intermittent fasting for other 6 months

Locations

Country Name City State
United States Washington University School of Medicine Saint Louis Missouri

Sponsors (1)

Lead Sponsor Collaborator
Washington University School of Medicine

Country where clinical trial is conducted

United States, 

References & Publications (1)

Goodrick CL, Ingram DK, Reynolds MA, Freeman JR, Cider NL. Effects of intermittent feeding upon growth and life span in rats. Gerontology. 1982;28(4):233-41. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change in HSCRP ( high sensitivity C-reactive protein) at 6 and 12 months HSCRP would be measured in mg/L Every 6 months- baseline, 6 month and 12 month
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