Vegetable Consumption in Relation to Health (8374)

February 27, 2012 updated by: W.J. Pasman, TNO

Beneficial Effects of Vegetable Consumption and a Diet Intervention on Health in Lean and Obese Men.

Rationale: Consumption of vegetables is generally considered to be associated with several positive effects on health. Vegetables are a heterogeneous group of our diet which is rich in bio-actives. The vegetables contain a range of vitamins, minerals, dietary fibres and phytochemicals like potassium, flavonoids, carotenoids, and vitamin C. The recommended intake of vegetables by the Dutch Health Council is 200 grams daily (Health Council, 2006).

Health in this project is defined as the possibility of a subject to change and adapt easily in response to a certain challenge. Healthy subjects show resilience in different physiological processes related to oxidative stress, metabolic stress, neurological stress and inflammatory stress. The reaction/response to a challenge might be changed when subjects have consumed more or less vegetables and have an improved health status. The response might also differentiate between subjects differing in BMI (healthy weight versus overweight/obese). Supplementation of vegetables will be provided in two conditions: a low and a high daily intake (50 versus 200 grams daily). An intervention known to have positive effects on health is weight loss. This will be studied in relation to health (the reaction to the challenge test) as well.

A beneficial effect is present when 5% improvement of health markers is shown with vegetable supplementation, similar as is known from weight loss studies.

Objective: The primary objective of the present study is to set-up a methodology to investigate health based on the resilience to challenge. A secondary objective is the effectiveness of the challenge concept with a food intervention. The vegetable supplementation study is a first example to test the challenge concept. Therefore, vegetable consumption according to the recommendations of the Dutch Health Council of 200 grams of vegetables daily will be studied with an exercise challenge test, to investigate the beneficial 'health' effects.

Study Overview

Detailed Description

Study design: The study is designed as a randomized, cross-over and parallel, open study.

Study population: The number of subjects participating in the study will be 32, healthy, lean and obese men, aged between 18-45 years.

Intervention: each intervention lasts four weeks:

  • High Vegetable treatment: consumption of 200 grams of vegetables daily;
  • Low Vegetable treatment: consumption of 50 grams of vegetables daily;
  • An energy restricted diet intervention with the habitual vegetable consumption.

Main study parameters/endpoints: A 'challenge test' will be used as a physical stress test to examine whether subjects show more or less resilience to the test. The reaction and recovery of the human system to the exercise test may be used as indicators of health status on different biological analyses (transcriptomics; metabolomics; rules based medicine pm). Different analyses to measure oxidative stress will be performed. Also standard health biomarkers will be determined to examine the intervention effects.

Study Type

Interventional

Enrollment (Actual)

32

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

    • Utrecht
      • Zeist, Utrecht, Netherlands, 3700 AJ
        • TNO Quality of Life, Metabolic ward

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

18 years to 45 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  1. Healthy as assessed by the

    • health and lifestyle questionnaire, (P8374 F02; in Dutch)
    • physical examination
    • results of the pre-study laboratory tests
  2. Males aged between 18 and 45 years at Day 01 of the study
  3. Body Mass Index (BMI): for the lean : between 20 and 25 kg/m2; obese between 30 and 35 kg/m2
  4. Normal Dutch eating habits as assessed by P8374 F02
  5. Used to consume vegetables daily and liking vegetables (P8374 F02 and F06)
  6. Physically able to perform a maximal cycling exercise test
  7. Voluntary participation
  8. Having given written informed consent
  9. Willing to comply with the study procedures
  10. Appropriate veins for blood sampling according to TNO
  11. Willing to accept use of all nameless data, including publication, and the confidential use and storage of all data for at least 15 years
  12. Willing to accept the disclosure of the financial benefit of participation in the study to the authorities concerned.

Exclusion Criteria:

  1. Participation in any clinical trial including blood sampling and/or administration of substances up to 90 days before Day 01 of this study
  2. Participation in any non-invasive clinical trial up to 30 days before Day 01 of this study, including no blood sampling and/or oral, intravenous, or inhalatory administration of substances
  3. Having a history of medical or surgical events that may significantly affect the study outcome, including cardiovascular disease or hypertension and/or (food) allergy
  4. Using prescribed medication or taking pain killers on a regular basis (judged by the medical investigator) ;
  5. Smoking
  6. Exercise regularly and exceed the Dutch Standard of Healthy Physical Activity of 2.5 hours/week
  7. Alcohol consumption > 28 units/week
  8. Reported unexplained weight loss or gain of > 2 kg in the month prior to the pre-study screening
  9. Reported slimming or medically prescribed diet
  10. Recent blood donation (<1 month prior to the start of the study)
  11. Not willing to give up blood donation during the study
  12. Personnel of TNO Quality of Life, their partner and their first and second degree relatives
  13. Not having a general practitioner
  14. Not willing to accept information-transfer concerning participation in the study, or information regarding his health, like laboratory results, findings at anamnesis or physical examination and eventual adverse events to and from his general practitioner.

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: High vegetable dose
Consumption of 200 grams of vegetables daily, for four weeks.
200 or 50 grams of vegetables daily for four weeks
Experimental: Low vegetable dose
Consumption of 50 grams of vegetables daily, for four weeks.
200 or 50 grams of vegetables daily for four weeks
Active Comparator: Weight loss interventio
Consumption of - 1000 kcal daily, for four weeks to be used as a positive control for the vegetables interventions.
Consume about 1000 kcal less daily, for four weeks, as a positive control to the vegetables interventions.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Investigate whether the maximal exercise performance test is a good concept for a challenge test, to examine 'health'. Health is defined as the ability to adapt in different circumstances.
Time Frame: after 4 weeks intervention
after 4 weeks intervention

Secondary Outcome Measures

Outcome Measure
Time Frame
Compare outcomes on the exercise test after high or low vegetable consumption and after weight loss. Differences are expected between the lean and obese subjects.
Time Frame: after four weeks of intervention
after four weeks of intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

TNO

Investigators

  • Principal Investigator: Wilrike Pasman, PhD, TNO
  • Study Director: Ineke Klöpping-Ketelaars, PhD, MD, TNO

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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, 2009

Primary Completion (Actual)

December 1, 2009

Study Completion (Actual)

December 1, 2010

Study Registration Dates

First Submitted

August 14, 2009

First Submitted That Met QC Criteria

August 14, 2009

First Posted (Estimate)

August 17, 2009

Study Record Updates

Last Update Posted (Estimate)

February 28, 2012

Last Update Submitted That Met QC Criteria

February 27, 2012

Last Verified

February 1, 2012

More Information

Terms related to this study

Other Study ID Numbers

  • P8374

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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