Effects of Food Cooking on Diabetes-2 Risk Factors

NCT ID: NCT01617304

Last Updated: 2013-01-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-12-31

Study Completion Date

2012-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The aim of the project is to investigate the effects of advanced glycation end products (AGEs) formed in food during the cooking process as well as AGEs formed naturally in the human body, on insulin sensitivity and risk factors for type 2 diabetes. The hypothesis is that i) food content of AGEs is lower using boiling and steaming cooking methods and that ii) AGEs formation in the body is lower at low dietary intake of certain sugar forms.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Obesity Type 2 Diabetes Insulin Resistance Cardiovascular Disease

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

low AGE, glucose

Food prepared by boiling/steaming and 20 g of glucose 3 times a day in a water solution

Group Type EXPERIMENTAL

Dietary intervention

Intervention Type OTHER

Food made by different cooking methods (boiling/steaming versus frying) and with glucose or fructose water solution

low AGE, fructose

Food prepared by boiling/steaming and 20 g of fructose 3 times a day in a water solution

Group Type EXPERIMENTAL

Dietary intervention

Intervention Type OTHER

Food made by different cooking methods (boiling/steaming versus frying) and with glucose or fructose water solution

high AGE, fructose

Food prepared by frying/baking and 20 g of fructose 3 times a day in a water solution

Group Type EXPERIMENTAL

Dietary intervention

Intervention Type OTHER

Food made by different cooking methods (boiling/steaming versus frying) and with glucose or fructose water solution

high AGE, glucose

Food prepared by frying/baking and 20 g of glucose 3 times a day in a water solution

Group Type EXPERIMENTAL

Dietary intervention

Intervention Type OTHER

Food made by different cooking methods (boiling/steaming versus frying) and with glucose or fructose water solution

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Dietary intervention

Food made by different cooking methods (boiling/steaming versus frying) and with glucose or fructose water solution

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* women, healthy between 20 and 50 y
* BMI between 25 and 40 kg/m2
* weight circumference over 88 cm

Exclusion Criteria

* weigh changes within the last 2 months more than +/- 3 kg
* Physical activity more than 8 h per week
* smoking
* medications and supplements
* being vegetarian or vegan
* pregnancy or breast feeding
* postmenopause
* chronic disease
* previous gastric bypass surgery
* blood donation within the last 3 months
* Involvement in other clinical trials
* allergic to paraaminobenzoic acid
Minimum Eligible Age

20 Years

Maximum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

The Ministry of Science, Technology and Innovation, Denmark

OTHER_GOV

Sponsor Role collaborator

University of Copenhagen

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

AAstrup

Head of Department

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Susanne G Bugel

Role: PRINCIPAL_INVESTIGATOR

Department of Human Nutrition, University of Copenhagen

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Department of Human Nutrition, University of Copenhagen

Frederiksberg, , Denmark

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Denmark

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

M201

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.