- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04075929
Short or Long High Intensity Training
Aerobic Short or Long High Intensity Interval Training - Does it Matter
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Studies among elite athletes have documented the importance of large amounts of training volume in order to perform at a high level in endurance sports. It is also well documented that both low intensity training (LIT), moderate intensity training (MIT) and high intensity training (HIT) should be included in the overall training efforts. It is well documented that HIT has a positive effect on the aerobic endurance among both elite athletes and recreational athletes.
Despite the fact that there is general agreement that HIT is an important part of the overall training, it is unclear how this part of the training should be organized in order to optimize the training effects. The adaptions of endurance performance seem to depend on both the intensity and the accumulated duration of the HIT sessions. Therefore, the aim of this study was to compare the effects of SI and LI training, including equal accumulated HIT duration, during a 4-week intervention period, conducted as 4x8-min with 2-min recovery periods, 4x(12x40/20-sec) with 2-min recovery periods and 4x(8x40/20-sec) with 2-min recovery periods, in different physiological- and performance parameters among well-trained cyclists.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Kristiansand, Norway, 4630
- University of Agder
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- male < 40 years,
- peak oxygen uptake (VO2peak) > 55 ml.kg-1.min-1,
- training volume >3 sessions per week (within cycling)
- absence of disease and injuries.
Exclusion Criteria:
- disease/injuries
- frequent absence of HIT sessions during the period.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: 4x8 min
4x8-min intervals with 2-min recovery periods.
The same accumulated duration of these three interval groups means that the total interval time is the same for each group: 4x8-min = 32 min
|
The cyclists were allowed to perform ad libitum low intensity (LIT) in addition to high intensity (HIT) sessions that were determined to each group.
The cyclists completed 12 supervised HIT sessions during the intervention period, three HIT sessions per week with at least 48 hours between each HIT-session.
All HIT sessions were performed as supervised group training sessions.
Each HIT session started with an individual 30 minutes' warm up at low intensity (55-70% HRmax) interspersed by freely chosen progressive sprints.
For all groups the power output during the recovery periods was 50 % of the power output used during work intervals.
The cyclists in all groups were instructed to perform each interval session at their maximal sustainable intensity.
Each session ended with 15-20 minutes' cool down (55-70% HRmax).
All HIT sessions were supervised and performed in groups on the University of Agder's (UiA) premises at Spicheren fitness center in Kristiansand.
|
Other: 4x(8x40/20s)
4x(12x40/20-sec) intervals with 2-min recovery periods The same accumulated duration of these three interval groups means that the total interval time is the same for each group:4x(12x40/20-sec) = 32 min if the 20-sec recovery is not included in the total time of HIT
|
The cyclists were allowed to perform ad libitum low intensity (LIT) in addition to high intensity (HIT) sessions that were determined to each group.
The cyclists completed 12 supervised HIT sessions during the intervention period, three HIT sessions per week with at least 48 hours between each HIT-session.
All HIT sessions were performed as supervised group training sessions.
Each HIT session started with an individual 30 minutes' warm up at low intensity (55-70% HRmax) interspersed by freely chosen progressive sprints.
For all groups the power output during the recovery periods was 50 % of the power output used during work intervals.
The cyclists in all groups were instructed to perform each interval session at their maximal sustainable intensity.
Each session ended with 15-20 minutes' cool down (55-70% HRmax).
All HIT sessions were supervised and performed in groups on the University of Agder's (UiA) premises at Spicheren fitness center in Kristiansand.
|
Other: 4x(12x40/20s)
4x(8x40/20-sec) intervals with 2-min recovery periods The same accumulated duration of these three interval groups means that the total interval time is the same for each group: 4x(8x40/20-sec) = 32 min if the 20-sec recovery is included in the total time of HIT
|
The cyclists were allowed to perform ad libitum low intensity (LIT) in addition to high intensity (HIT) sessions that were determined to each group.
The cyclists completed 12 supervised HIT sessions during the intervention period, three HIT sessions per week with at least 48 hours between each HIT-session.
All HIT sessions were performed as supervised group training sessions.
Each HIT session started with an individual 30 minutes' warm up at low intensity (55-70% HRmax) interspersed by freely chosen progressive sprints.
For all groups the power output during the recovery periods was 50 % of the power output used during work intervals.
The cyclists in all groups were instructed to perform each interval session at their maximal sustainable intensity.
Each session ended with 15-20 minutes' cool down (55-70% HRmax).
All HIT sessions were supervised and performed in groups on the University of Agder's (UiA) premises at Spicheren fitness center in Kristiansand.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Maximal oxygen uptake
Time Frame: 4 weeks
|
VO2max
|
4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Functional threshold power
Time Frame: 4 weeks
|
FTP
|
4 weeks
|
Peak power output
Time Frame: 4 weeks
|
PPO
|
4 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Monica K. Torstveit, Professor, Universitetet i Agder
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Aerobic short og long interval
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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