- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02006394
Novel Dietary Interventions for Treating Insulin Resistance
December 10, 2013 updated by: Dorothy Sears, University of California, San Diego
Clinical and rodent studies have demonstrated the impact of specific dietary factors in modulating inflammation-related diseases including insulin resistance, type 2 diabetes, and cardiovascular disease.
Such dietary factors include polyunsaturated fats, polyphenols, and glycemic index.
The investigators know from previous studies in the literature that reducing the glycemic index and increasing the omega-3 fat and polyphenol content of the diet results in improved metabolic indices and reduced inflammation.
These improvements can be observed even within the context of persistent obesity.
The investigators will implement a reduced-calorie, multi-pronged dietary approach for improving insulin sensitivity and reducing inflammation in obese subjects with the metabolic syndrome.
The active diet will include reduced glycemic index foods together with omega-3 fats and polyphenol supplements.
The primary hypothesis is that the dietary combination of reduced glycemic index foods, omega-3 fats and polyphenols will work to reduce insulin resistance and inflammation more efficiently than a placebo-controlled, calorie- and macronutrient-matched diet in obese subjects with the metabolic syndrome.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
41
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
San Diego, California, United States, 92093
- University of California, San Diego
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
21 years to 55 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Body Mass Index (BMI): 30.0-40.9 kg/m^2
- Metabolic Syndrome
Exclusion Criteria:
- Diabetes
- Inflammatory diseases
- Eating disorders
- Pregnancy
- Known kidney, coronary, gastrointestinal or peripheral artery disease
- Smoking
- Recent fish oil (>500mg eicosapentaenoic acid (EPA) + docosahexaenoic acid (DHA)/day) or polyphenol supplement use
- Recent weight change
- Strenuous exercise
- Fish/food allergies
- Current diabetic, lipid-lowering (fibrates, statins), anti-inflammatory, immune-suppressant, and/or anti-inflammatory hypertension medication use
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Active Diet
Reduced glycemic index bread products, fish oil capsules, and polyphenol capsules.
|
fish oil capsules
delphinidin polyphenol capsules
Made by Zone Labs
|
|
Placebo Comparator: Placebo Diet
Market variety bread products, corn oil capsules, and corn starch capsules.
|
Corn Oil Capsules
Maltodextrin capsules
placebo bread products
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in insulin resistance
Time Frame: Baseline, 6 weeks, and 12 weeks
|
Fasting plasma insulin, Homeostasis Model of Assessment - Insulin Resistance (HOMA-IR)
|
Baseline, 6 weeks, and 12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in inflammation biomarkers
Time Frame: Baseline, 6 weeks, 12 weeks
|
Fasting plasma cytokines and C-reactive protein (CRP), monocyte expression of inflammatory genes
|
Baseline, 6 weeks, 12 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in adipokines
Time Frame: Baseline, 6 weeks, 12 weeks
|
Fasting plasma adiponectin and leptin
|
Baseline, 6 weeks, 12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Dorothy Sears, PhD, University of California, San Diego
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2012
Primary Completion (Actual)
July 1, 2013
Study Completion (Actual)
November 1, 2013
Study Registration Dates
First Submitted
December 4, 2013
First Submitted That Met QC Criteria
December 4, 2013
First Posted (Estimate)
December 10, 2013
Study Record Updates
Last Update Posted (Estimate)
December 12, 2013
Last Update Submitted That Met QC Criteria
December 10, 2013
Last Verified
December 1, 2013
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB #110549
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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