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The Influence of a High Intensity Physical Activity Intervention on a Selection of Health Related Outcomes: An Ecological Approach

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ClinicalTrials.gov Identifier: NCT01027156
Recruitment Status : Completed
First Posted : December 7, 2009
Last Update Posted : December 7, 2009
Sponsor:
Collaborator:
Swansea University
Information provided by:
University of the West of Scotland

Brief Summary:
The purpose of this study is to determine whether a High Intensity exercise intervention can elicit cardiovascular disease protection in adolescents.

Condition or disease Intervention/treatment Phase
To Assess the Impact of the HIT Intervention on Physiological Responses To Assess the Role of a Secondary High School as a Setting for Promoting Healthy Eating and PA Behaviours To Determine the Associations Between CVD Risk Factors at Baseline in 15 - 18 Year Old Youth Behavioral: High Intensity Exercise Not Applicable

Study Type : Interventional  (Clinical Trial)
Primary Purpose: Prevention
Study Start Date : October 2009
Actual Primary Completion Date : December 2009
Actual Study Completion Date : December 2009

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: High Intensity Exercise Behavioral: High Intensity Exercise
In this study, participants will be instructed to sprint maximally for a period of 30 seconds. Following 30s rest, the participants will be instructed to repeat this procedure a further 3 times. This equates to 2 minutes of maximal effort sprinting interspersed with 2 minutes recovery. Participants will be requested to perform this protocol 3 times weekly. Training progression will be implemented by increasing the number of repeats from four repetitions during weeks 1 and 2, to five repetitions during weeks 3 and 4, to six repetitions during weeks 5 and 6. Finally, during week 7 participants will still perform six repetitions but interspersed by only 20 s recovery.




Primary Outcome Measures :
  1. To improve blood lipid profiles and lower levels of plasma inflammatory markers.

Secondary Outcome Measures :
  1. To determine the associations between CVD risk factors at baseline in 15 - 18 year old youth.


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Ages Eligible for Study:   15 Years to 18 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Healthy
  • 15 - 18 yer old that are capable of performing vigorous exercise

Exclusion Criteria:

  • Any health condition that would prevent them from undertaking vigorous exercise

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): NCT01027156


Locations
United Kingdom
Holy Cross High School
Hamilton, South Lanarkshire, United Kingdom, ML3 0BN
Sponsors and Collaborators
University of the West of Scotland
Swansea University

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Duncan Buchan, Lecturer, University of the West of Scotland
ClinicalTrials.gov Identifier: NCT01027156     History of Changes
Other Study ID Numbers: HI Intervention
First Posted: December 7, 2009    Key Record Dates
Last Update Posted: December 7, 2009
Last Verified: December 2009

Keywords provided by University of the West of Scotland:
Public Health
Biochemistry
Ecological