search
Back to results

Weight Loss and Changes in Cardiovascular Risk Markers With a Low Glycemic Diet Compared With a Standard Diet

Primary Purpose

Obesity, Metabolic Syndrome

Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Diet counseling
Sponsored by
Ullevaal University Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Obesity focused on measuring Obesity,, weight loss,, diet counseling, low-glycemic load

Eligibility Criteria

30 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Men or women age 30-65, BMI in the range 28-35 kg/m2 for women and 28-40kg/m2 for men. At least one of the following components of the metabolic syndrome; fasting triglycerides > 1,7, fasting glucose 6,0-6,9, HDL-cholesterol <1,03 (males) or <1,29 (females), Blood pressure >130/85 (with or without treatment), diet-treated diabetes mellitus or drug treated hypertension. Stable weight range of 4 kg or less the last 12 weeks, No major change in physical activity the last 12 weeks Exclusion Criteria: Any symptomatic cardiovascular disease Diabetes requiring drug treatment Currently on special diet Hepatic/renal dysfunction Hypothyroidism (unstable) GI disorder impairing compliance with diet recommendation, History of unstable psychiatric or medical disorder, Need of lipid lowering drug, Alcohol or drug abuse, Participation in drug trial the last 30 days, Use of drugs for weight reduction last 12 weeks, pregnancy or planned pregnancy, Obesity of known endocrine origin, history of obesity surgery, Uncontrolled hypertension (>160/100), Previous participation in >3 weight reduction programs, or within last 12 months, Not willing to be randomized, Individual judged to be unable to follow instructions and procedures of the study

Sites / Locations

  • Ulleval University Hospital, dep. of preventive cardiology

Outcomes

Primary Outcome Measures

The primary objective will be to compare the effects of the two different diet recommendations with respect to the one-year change in body weight.

Secondary Outcome Measures

Compare the consequences of the two strategies with respect to 3, 6, and 12 months development of the variables; glucose/insulin,
insulin sensitivity index,
number of metabolic syndrome factors,
high sensitive C-reactive protein,
lipids and lipoprotein B and
anthropometric indices (waist /hip ratio)
Fat cell hormones (leptin, adiponectin, ghrelin)
Inflammation markers (ICAM).
Weight at 18 months follow-up.

Full Information

First Posted
September 30, 2005
Last Updated
June 30, 2011
Sponsor
Ullevaal University Hospital
Collaborators
Norges Forskningsråd, Stenberggata 26, pb. 2700, N-0131 Oslo, Norway
search

1. Study Identification

Unique Protocol Identification Number
NCT00230919
Brief Title
Weight Loss and Changes in Cardiovascular Risk Markers With a Low Glycemic Diet Compared With a Standard Diet
Official Title
Weight Loss and Changes in Cardiovascular Risk Markers With a Low Glycemic Load Diet Compared With a Standard National Nutrition Council-recommended Diet: a Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2004
Overall Recruitment Status
Completed
Study Start Date
April 2004 (undefined)
Primary Completion Date
June 2006 (Actual)
Study Completion Date
November 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Ullevaal University Hospital
Collaborators
Norges Forskningsråd, Stenberggata 26, pb. 2700, N-0131 Oslo, Norway

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Overweight and obesity is increasing in most countries, including Norway, and the optimal diet for reducing weight is under discussion. The present study in overweight and moderate obese individuals compares a low glycemic load diet with a standard low-fat diet (as recommended from the National Nutrition Council) in an open, randomized trial over 12 months, with changes in weight loss and changes in cardiovascular risk markers as endpoints.
Detailed Description
Overweight and obesity is rapidly increasing in most countries, including Norway, and at present there is controversy regarding what diet should be recommended for reducing weight and the complications of obesity. The present study is performed in in 200 overweight and moderate obese individuals, that is in men with body mass index (BMI) from 28 to 40, and women with BMI 28-35. To be included, the participants should also have at least one component of the metabolic syndrome. After a medical examination and check for inclusion and exclusion criteria, the participants are randomized to one the two following diets: 1) A low-glycemic load diet aiming at a macronutrient composition with 25-30% of energy from protein, 35-40% from fat and 30-35% from carbohydrate or 2) A low-fat diet aiming at a macronutrient composition with 15% of energy from protein, 25-30% from fat and 55-60% from carbohydrate. Each group will have 9 dietary counselling sessions in the course of the study; baseline, week 2, month 1,3,4,5,6 and 9. Recommended total energy intake will be individualized based on the metabolic rate at rest for each subject, and using a physical activity level of 1,4. A 500 kcal/day deficit relative to the daily energy requirements will be recommended. The primary objective will be to compare the effects of the two different diet recommendations with respect to the one-year change in body weight. As secondary objectives the study will compare the consequences of the two strategies with respect to 3, 6, and 12 months development of the variables glucose/insulin, insulin sensitivity index, number of metabolic syndrome factors, high sensitive C-reactive protein, lipids, lipoprotein B and anthropometric indices (waist /hip ratio). Serum will be frozen for additional parameters as leptin, adiponectin, ghrelin and ICAM. Also to be studied is an additional weight at 18 months follow-up, when no more advice is given past the 9-month visit.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Metabolic Syndrome
Keywords
Obesity,, weight loss,, diet counseling, low-glycemic load

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (false)

8. Arms, Groups, and Interventions

Intervention Type
Behavioral
Intervention Name(s)
Diet counseling
Primary Outcome Measure Information:
Title
The primary objective will be to compare the effects of the two different diet recommendations with respect to the one-year change in body weight.
Secondary Outcome Measure Information:
Title
Compare the consequences of the two strategies with respect to 3, 6, and 12 months development of the variables; glucose/insulin,
Title
insulin sensitivity index,
Title
number of metabolic syndrome factors,
Title
high sensitive C-reactive protein,
Title
lipids and lipoprotein B and
Title
anthropometric indices (waist /hip ratio)
Title
Fat cell hormones (leptin, adiponectin, ghrelin)
Title
Inflammation markers (ICAM).
Title
Weight at 18 months follow-up.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men or women age 30-65, BMI in the range 28-35 kg/m2 for women and 28-40kg/m2 for men. At least one of the following components of the metabolic syndrome; fasting triglycerides > 1,7, fasting glucose 6,0-6,9, HDL-cholesterol <1,03 (males) or <1,29 (females), Blood pressure >130/85 (with or without treatment), diet-treated diabetes mellitus or drug treated hypertension. Stable weight range of 4 kg or less the last 12 weeks, No major change in physical activity the last 12 weeks Exclusion Criteria: Any symptomatic cardiovascular disease Diabetes requiring drug treatment Currently on special diet Hepatic/renal dysfunction Hypothyroidism (unstable) GI disorder impairing compliance with diet recommendation, History of unstable psychiatric or medical disorder, Need of lipid lowering drug, Alcohol or drug abuse, Participation in drug trial the last 30 days, Use of drugs for weight reduction last 12 weeks, pregnancy or planned pregnancy, Obesity of known endocrine origin, history of obesity surgery, Uncontrolled hypertension (>160/100), Previous participation in >3 weight reduction programs, or within last 12 months, Not willing to be randomized, Individual judged to be unable to follow instructions and procedures of the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tor Ole Klemsdal, MD, Ph.D
Organizational Affiliation
Ullevaal University Hospital, preventive medicine clinic
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Serena Tonstad, MD, Ph.D
Organizational Affiliation
Ullevaal University Hospital, preventive medicine clinic
Official's Role
Study Chair
Facility Information:
Facility Name
Ulleval University Hospital, dep. of preventive cardiology
City
Oslo
ZIP/Postal Code
N-0407
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
19502017
Citation
Klemsdal TO, Holme I, Nerland H, Pedersen TR, Tonstad S. Effects of a low glycemic load diet versus a low-fat diet in subjects with and without the metabolic syndrome. Nutr Metab Cardiovasc Dis. 2010 Mar;20(3):195-201. doi: 10.1016/j.numecd.2009.03.010. Epub 2009 Jun 6.
Results Reference
result
PubMed Identifier
22889406
Citation
Heggen E, Klemsdal TO, Haugen F, Holme I, Tonstad S. Effect of a low-fat versus a low-gycemic-load diet on inflammatory biomarker and adipokine concentrations. Metab Syndr Relat Disord. 2012 Dec;10(6):437-42. doi: 10.1089/met.2012.0012. Epub 2012 Aug 13.
Results Reference
derived

Learn more about this trial

Weight Loss and Changes in Cardiovascular Risk Markers With a Low Glycemic Diet Compared With a Standard Diet

We'll reach out to this number within 24 hrs