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Supplementary Intake of Vitamin D During 12 Weeks Strength Training in Younger and Older People

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ClinicalTrials.gov Identifier: NCT01252381
Recruitment Status : Completed
First Posted : December 3, 2010
Last Update Posted : July 5, 2017
Sponsor:
Collaborator:
Institute of Sports Medicine, Copenhagen
Information provided by (Responsible Party):
Jakob Agergaard, Bispebjerg Hospital

Brief Summary:

The aim is to investigate the importance of vitamin D levels to achieve the effect of strength training. If we can show that vitamin D has an effect of training, the ultimate goal is to find out why and how vitamin D affects muscle.

This would potentially have important implications for public health. Since a large number of populations, including elderly, are shown to have too little vitamin D and also has low muscle strength, it will be essential that these people added vitamin D in relation to training and rehabilitation.


Condition or disease Intervention/treatment Phase
Muscle Strength Tendon Elasticity Muscle CSA Tendon CSA VDR Receptor Other: 12 weeks Strength exercise training Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 40 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Other
Official Title: The Importance of Supplementary Intake of Vitamin D on the Efficacy of 12 Weeks of Strength Training in Both Vitamin D Sufficient Younger and Older People
Study Start Date : November 2010
Actual Primary Completion Date : February 2012
Actual Study Completion Date : January 2013

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Vitamin D
Drug Information available for: Vitamin D

Arm Intervention/treatment
Active Comparator: Vitamin D Other: 12 weeks Strength exercise training
Training 3 times a week, leg extensions and leg press

Placebo Comparator: Calcium tablet Other: 12 weeks Strength exercise training
Training 3 times a week, leg extensions and leg press




Primary Outcome Measures :
  1. Cross-sectional area of thigh musculature and knee tendon [ Time Frame: 12 weeks ]
  2. VDR potential target CYP27b1 [ Time Frame: 12 weeks ]


Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 75 Years   (Adult, Older Adult)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Men 20-30 or 60-75 years old

Exclusion Criteria:

  • smokers Knee problems On medication affecting protein synthesis High exposure to sun light (ex. ski holiday) during the trial

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 ClinicalTrials.gov identifier (NCT number): NCT01252381


Locations
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Denmark
Institute of Sports Medicine - Bispebjerg Hospital
Copenhagen, Denmark, DK-2400
Sponsors and Collaborators
Bispebjerg Hospital
Institute of Sports Medicine, Copenhagen
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Jakob Agergaard, MSc, PhD Student, Bispebjerg Hospital
ClinicalTrials.gov Identifier: NCT01252381    
Other Study ID Numbers: BBH 77
First Posted: December 3, 2010    Key Record Dates
Last Update Posted: July 5, 2017
Last Verified: July 2017