Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
18 participants
INTERVENTIONAL
2015-12-31
2016-03-31
Brief Summary
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Detailed Description
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Objective:
The main objective is to investigate whether ionized magnesium concentration varies during one day, and whether it is changed after one bout of exercise
Study design:
This will be a cross-over design. With screening and preliminary tests before the exercise test day and the non-exercise test day. The order in which exercise day and non-exercise day will be done, will be randomly divided between the participants.
Intervention:
A rest day and an exercise day At exercise day: an exercise test of 90 min at 70% of VO2max. Blood samples are taken at set time points during rest day and exercise day
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
NONE
Study Groups
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Exercise day
Behavioral intervention: 90min bike ergometer test at 70% of VO2max. Blood samples are collected at set time points (08:30, 11:00, 12:30, 13:30, 15:00, 16:00 and 18:30). Blood samples are analyzed on the pHOx analyzer for their ionized magnesium concentration. And on the Dimension Vista 1500 from Siemens for their total magnesium concentration.
Exercise protocol
70% VO2max bike ergometer test for 90 minutes
Non exercise day (Rest day)
No exercise protocol. Estimating daily variation of magnesium concentration. Blood samples are collected at set time points (08:30, 11:00, 12:30, 13:30, 15:00, 16:00 and 18:30). Blood samples are analyzed on the pHOx analyzer for their ionized magnesium concentration. And on the Dimension Vista 1500 from Siemens for their total magnesium concentration.
No interventions assigned to this group
Interventions
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Exercise protocol
70% VO2max bike ergometer test for 90 minutes
Eligibility Criteria
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Inclusion Criteria
* BMI: 18.5 - 25
* Minimal of 5 hours of training per week, for at least 2 years
* Used to bike, at least 5 hours per week in high season
* No Mg and / or Ca supplementation during study
* No blood donation, during or in the 6 weeks preliminary the study
* Suitable veins
* No chronic medication, with the exception of paracetamol and or birth control
* No antibiotics in the month preliminary the study
* Good health
* Serum Mg \> 0.7 mmol/L
* Willing to give blood
* Able to be present and participate at all test days
Exclusion Criteria
* Use of medication with the exception of paracetamol and or birth control
* Mg and or Ca supplementation use
* Inadequate Mg intake (according to FFQ)
* Working at Human Nutrition
* Wageningen University Msc thesis or internship at Human Nutrition
* Participating in other scientific research (with the exception of EetMeetWeet)
18 Years
45 Years
ALL
Yes
Sponsors
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Gelderse Vallei Hospital
OTHER
Wageningen University
OTHER
Responsible Party
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Principal Investigators
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Jacqueline Klein Gunnewiek, Phd
Role: PRINCIPAL_INVESTIGATOR
Gelderse Vallei Hospital
Other Identifiers
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NL54333.081.15
Identifier Type: -
Identifier Source: org_study_id
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