Interval Training in Young Healthy Individuals

NCT ID: NCT00733941

Last Updated: 2015-05-27

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

24 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-09-30

Study Completion Date

2009-12-31

Brief Summary

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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

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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.

Conditions

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Healthy Subjects Exercise Test

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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High frequency training

24 interval exercises performed 8 times per week

Group Type EXPERIMENTAL

High frequency training

Intervention Type BEHAVIORAL

24 training sessions, 8x weekly, followed by detraining phase 8 weeks, and retraining

Normal frequency training

24 interval exercises performed 3 times per week

Group Type EXPERIMENTAL

normal frequence training

Intervention Type BEHAVIORAL

24 training sessions, 3x weekly, followed by detraining phase 8 weeks, and retraining

Interventions

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High frequency training

24 training sessions, 8x weekly, followed by detraining phase 8 weeks, and retraining

Intervention Type BEHAVIORAL

normal frequence training

24 training sessions, 3x weekly, followed by detraining phase 8 weeks, and retraining

Intervention Type BEHAVIORAL

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

27 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Norwegian University of Science and Technology

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Øivind Rognmo, PhD

Role: PRINCIPAL_INVESTIGATOR

Norwegian University of Science and Technology

Ulrik Wisløff, Professor

Role: PRINCIPAL_INVESTIGATOR

National Taiwan Normal University

Locations

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Norwegian University of Science and Technology

Trondheim, , Norway

Site Status

NTNU

Trondheim, , Norway

Site Status

Countries

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Norway

References

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Hatle H, Stobakk PK, Molmen HE, Bronstad E, Tjonna AE, Steinshamn S, Skogvoll E, Wisloff U, Ingul CB, Rognmo O. Effect of 24 sessions of high-intensity aerobic interval training carried out at either high or moderate frequency, a randomized trial. PLoS One. 2014 Feb 7;9(2):e88375. doi: 10.1371/journal.pone.0088375. eCollection 2014.

Reference Type RESULT
PMID: 24516645 (View on PubMed)

Other Identifiers

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4.2008.1755

Identifier Type: -

Identifier Source: org_study_id

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