NCT04075929

Brief Summary

To compare the effects of short and long high intensity interval training (HIT) conducted with the same total accumulated duration on physiological- and performance parameters during a 4-week training period.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
22

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Nov 2017

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2017

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 15, 2017

Completed
5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

December 20, 2017

Completed
1.7 years until next milestone

First Submitted

Initial submission to the registry

August 29, 2019

Completed
5 days until next milestone

First Posted

Study publicly available on registry

September 3, 2019

Completed
Last Updated

September 3, 2019

Status Verified

August 1, 2019

Enrollment Period

1 month

First QC Date

August 29, 2019

Last Update Submit

August 30, 2019

Conditions

Keywords

Cyclingendurance performanceintermittent exercisemaximal oxygen consumptionphysiological adaptionswell-trained athletes

Outcome Measures

Primary Outcomes (1)

  • Maximal oxygen uptake

    VO2max

    4 weeks

Secondary Outcomes (2)

  • Functional threshold power

    4 weeks

  • Peak power output

    4 weeks

Study Arms (3)

4x8 min

OTHER

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

Other: Training effects on aerobic output

4x(8x40/20s)

OTHER

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

Other: Training effects on aerobic output

4x(12x40/20s)

OTHER

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

Other: Training effects on aerobic output

Interventions

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.

4x(12x40/20s)4x(8x40/20s)4x8 min

Eligibility Criteria

Age18 Years - 40 Years
Sexmale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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.

You may not qualify if:

  • disease/injuries
  • frequent absence of HIT sessions during the period.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Agder

Kristiansand, 4630, Norway

Location

Study Officials

  • Monica K. Torstveit, Professor

    Universitetet i Agder

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

August 29, 2019

First Posted

September 3, 2019

Study Start

November 1, 2017

Primary Completion

December 15, 2017

Study Completion

December 20, 2017

Last Updated

September 3, 2019

Record last verified: 2019-08

Data Sharing

IPD Sharing
Will not share

Locations