Dairy Products and Metabolic Syndrome

Sponsor
Norwegian University of Life Sciences (Other)
Overall Status
Completed
CT.gov ID
NCT01913756
Collaborator
Tine (Industry)
153
1
3
3
51.2

Study Details

Study Description

Brief Summary

The purpose of this trial is to investigate the effect of dairy products on the so called metabolic syndrome. Metabolic syndrome is a cluster of risk factors, such as high blood pressure and high cholesterol, for the development of diabetes and heart disease. Participants will be randomly assigned to either eat a portion of a Norwegian traditional cheese which is high in protein and low in fat (group 1), or eat a slightly higher than normal intake of regular Gouda-type cheese (group 2), or to limit their intake of cheese (group 3).

Dairy products are a significant source of bioactive peptides, small pieces of protein which may have an effect on our health. These effects may be antimicrobial, antioxidative, or blood pressure lowering. The traditional Norwegian cheese, Gamalost, which is naturally high in protein (50%) and low in fat (<1%), has been found to be particularly high in these bioactive peptides. Specifically, the cheese was found to have a very high ACE-inhibitory activity, meaning it has the potential to lower blood pressure without the use of pharmaceuticals.

A pilot study was performed in May 2012. No intervention was given in this trial, but participants answered an extensive questionnaire about dietary habits and lifestyle. This trial found that the people who ate the most Gamalost had a slightly lower blood pressure than those that did not eat the cheese. Since that was just a point-in-time study with no intervention or control, the investigators are not able to say anything certain about cause and effect, which is why the investigators want to perform this larger controlled study.

In total, the investigators aim to recruit 300 people to participate in this trial, i.e. 100 in each group. The participants will be randomly placed in one of the groups and they will have to do the intervention for eight weeks. At inclusion, the investigators measure blood pressure, fasting blood glucose, weight, height, waist circumference, and the investigators draw a fasting blood sample to measure cholesterol. The same measurements will be repeated at the end of the eight weeks. At inclusion they will also fill out an extensive questionnaire about their diet and lifestyle. A shorter version of the same questionnaire will also be given at the end of the trial period.

The overall goal of the study is to assess the effect of dairy products on the metabolic syndrome, but the main hypothesis is to assess whether a high intake of Gamalost can reduce blood pressure in a group of people.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Gamalost (Norwegian traditional cheese)
  • Dietary Supplement: Gouda-type cheese
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
153 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Prevention
Study Start Date :
Apr 1, 2013
Actual Primary Completion Date :
Jul 1, 2013
Actual Study Completion Date :
Jul 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Experimental: Gouda-type cheese

80 g/day Gouda-type cheese

Dietary Supplement: Gouda-type cheese

No Intervention: Low cheese intake

Experimental: Gamalost (Norwegian traditional cheese)

50 g/day Gamalost

Dietary Supplement: Gamalost (Norwegian traditional cheese)

Outcome Measures

Primary Outcome Measures

  1. Change in blood pressure [Baseline, 4 weeks and 8 weeks.]

Secondary Outcome Measures

  1. Change in serum cholesterol levels [Baseline and 8 weeks.]

  2. Change in body composition. [Baseline and 8 weeks.]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Healthy adults

  • Must be able to eat cheese evey day

Exclusion Criteria:
  • Pregnant women

  • Taking blood pressure lowering medication

  • Not able to read Norwegian

Contacts and Locations

Locations

Site City State Country Postal Code
1 Norwegian University of Life Sciences Aas Norway 1432

Sponsors and Collaborators

  • Norwegian University of Life Sciences
  • Tine

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Rita Nilsen, PhD Student, Norwegian University of Life Sciences
ClinicalTrials.gov Identifier:
NCT01913756
Other Study ID Numbers:
  • REK-340857
First Posted:
Aug 1, 2013
Last Update Posted:
Nov 18, 2014
Last Verified:
Nov 1, 2014
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 18, 2014