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Clinical Trials/NCT00733941
NCT00733941CompletedNot Applicable

Interval Training: Training, Detraining and Retraining; an Interventional Study

Norwegian University of Science and Technology2 sites in 1 country24 target enrollmentStarted: September 1, 2008Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
24
Locations
2
Primary Endpoint
Oxygen uptake

Study Overview

Brief Summary

Individuals who participate in regular physical exercise possess a lower prevalence of cardiovascular risk factors such as hypertension, type 2 diabetes, obesity and hypercholesterolemia, and aerobic exercise is therefore considered an important adjuvant therapy in risk factor modification and to promote health.

The main focus of the present study is therefore to detect how rapid it is possible to increase aerobic capacity with interval running exercise.

The hypothesis is that it is possible to improve maximal oxygen uptake faster when increasing training frequency. The total gain in maximal oxygen uptake will however be the same between the two groups when they have performed the same amount of training

Detailed Description

We will perform aerobic interval training at an intensity of 90-95% of maximum heart rate in healthy individuals. The subjects will be randomly assigned to carry out a total of 24 exercise-sessions, either at 3 times per week or 8 times per week.

The two groups will carry out 24 training sessions before 8 weeks of detraining will provide how rapidly aerobic capacity is lost due to inactivity. After the detraining period a retraining phase is introduced to detect if improvements in aerobic capacity occur more rapidly compared to before the first training period

The subjects will be tested for oxygen uptake, pumping capacity of the heart, blood volume, skeletal muscle enzyme activity, endothelial function.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 27 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •BMI<27, non-smokers, train less that 1-2 times per week, VO2max <60 for male and <50 for female.

Exclusion Criteria

  • •Hypertension, diabetes and cardiovascular disease.

Arms & Interventions

High frequency training

Experimental

24 interval exercises performed 8 times per week

Intervention: High frequency training (Behavioral)

Normal frequency training

Experimental

24 interval exercises performed 3 times per week

Intervention: normal frequence training (Behavioral)

Outcomes

Primary Outcomes

Oxygen uptake

Time Frame: Before and after the training-, detraining- and retraining-phase

Secondary Outcomes

  • Cardiac function and skeletal muscle enzyme activity(After training, detraining and retraining)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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