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Vegetable Consumption in Relation to Health (8374)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00959790
Recruitment Status : Completed
First Posted : August 17, 2009
Last Update Posted : February 28, 2012
Netherlands: Ministry of Health, Welfare and Sports
Information provided by (Responsible Party):
W.J. Pasman, TNO

Brief Summary:

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.

Condition or disease Intervention/treatment Phase
Health Obesity Oxidative Stress Dietary Supplement: Vegetables Dietary Supplement: energy restriction Not Applicable

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.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 32 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Basic Science
Official Title: Beneficial Effects of Vegetable Consumption and a Diet Intervention on Health in Lean and Obese Men.
Study Start Date : January 2009
Actual Primary Completion Date : December 2009
Actual Study Completion Date : December 2010

Arm Intervention/treatment
Experimental: High vegetable dose
Consumption of 200 grams of vegetables daily, for four weeks.
Dietary Supplement: Vegetables
200 or 50 grams of vegetables daily for four weeks

Experimental: Low vegetable dose
Consumption of 50 grams of vegetables daily, for four weeks.
Dietary Supplement: Vegetables
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.
Dietary Supplement: energy restriction
Consume about 1000 kcal less daily, for four weeks, as a positive control to the vegetables interventions.

Primary Outcome Measures :
  1. 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 ]

Secondary Outcome Measures :
  1. 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 ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes

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.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00959790

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TNO Quality of Life, Metabolic ward
Zeist, Utrecht, Netherlands, 3700 AJ
Sponsors and Collaborators
Netherlands: Ministry of Health, Welfare and Sports
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Principal Investigator: Wilrike Pasman, PhD TNO
Study Director: Ineke Klöpping-Ketelaars, PhD, MD TNO

Publications automatically indexed to this study by Identifier (NCT Number):
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Responsible Party: W.J. Pasman, TNO, Zeist, The Netherlands, TNO Identifier: NCT00959790    
Other Study ID Numbers: P8374
First Posted: August 17, 2009    Key Record Dates
Last Update Posted: February 28, 2012
Last Verified: February 2012
Keywords provided by W.J. Pasman, TNO:
Oxidative stress
Challenge concept
Additional relevant MeSH terms:
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Nutrition Disorders
Body Weight
Signs and Symptoms