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Effect of Floorball on Healthy Subjects

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.
 
ClinicalTrials.gov Identifier: NCT03371238
Recruitment Status : Active, not recruiting
First Posted : December 13, 2017
Last Update Posted : May 29, 2019
Sponsor:
Information provided by (Responsible Party):
Morten Hostrup, PhD, University of Copenhagen

Brief Summary:
To investigate the effect of floorball on health and performance in healthy subjects over 65 years.

Condition or disease Intervention/treatment Phase
Aging Problems Behavioral: Floorball Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 500 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Basic Science
Official Title: The Effect of Floorball on Health and Performance Parameters in Healthy Seniors
Actual Study Start Date : September 14, 2017
Actual Primary Completion Date : May 27, 2019
Estimated Study Completion Date : June 2020

Arm Intervention/treatment
Experimental: Floorball Behavioral: Floorball
The subjects in this group are set to play floorball three times pr. week for 39 weeks.

No Intervention: Control



Primary Outcome Measures :
  1. Echocardiogram [ Time Frame: Changes from baseline measured after 12 weeks and 39 weeks ]
    The measure of the hearts geometric dimensions

  2. Bodycomposition [ Time Frame: Changes from baseline measured after 12 weeks and 39 weeks ]
    DXA scan



Information from the National Library of Medicine

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Ages Eligible for Study:   65 Years to 85 Years   (Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Healthy
  • age 65-85
  • physical activity <2 hours pr. week.

Exclusion Criteria:

  • age <18 years
  • Injuries that prevent the subject from playing floorball
  • Alcohol >14 units pr. week.
  • Pregnancy
  • Other serious conditions

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): NCT03371238


Locations
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Denmark
August Krogh Building
Copenhagen, Denmark
Sponsors and Collaborators
University of Copenhagen
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Responsible Party: Morten Hostrup, PhD, PhD, University of Copenhagen
ClinicalTrials.gov Identifier: NCT03371238    
Other Study ID Numbers: MFloorball
First Posted: December 13, 2017    Key Record Dates
Last Update Posted: May 29, 2019
Last Verified: May 2019

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No