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.

Abstract

Purpose: The training response of an intensified period of high-intensity exercise is not clear. Therefore, we compared the cardiovascular adaptations of completing 24 high-intensity aerobic interval training sessions carried out for either three or eight weeks, respectively.

Methods: Twenty-one healthy subjects (23.0±2.1 years, 10 females) completed 24 high-intensity training sessions throughout a time-period of either eight weeks (moderate frequency, MF) or three weeks (high frequency, HF) followed by a detraining period of nine weeks without any training. In both groups, maximal oxygen uptake (VO2max) was evaluated before training, at the 9(th) and 17(th) session and four days after the final 24(th) training session. In the detraining phase VO2max was evaluated after 12 days and thereafter every second week for eight weeks. Left ventricular echocardiography, carbon monoxide lung diffusion transfer factor, brachial artery flow mediated dilatation and vastus lateralis citrate maximal synthase activity was tested before and after training.

Results: The cardiovascular adaptation after HF training was delayed compared to training with MF. Four days after ending training the HF group showed no improvement (+3.0%, p = 0.126), whereas the MF group reached their highest VO2max with a 10.7% improvement (p<0.001: group difference p = 0.035). The HF group reached their highest VO2max (6.1% increase, p = 0.026) twelve days into the detraining period, compared to a concomitant reduction to 7.9% of VO2max (p<0.001) above baseline in the MF group (group difference p = 0.609).

Conclusion: Both HF and MF training of high-intensity aerobic exercise improves VO2max. The cardiovascular adaptation following a HF programme of high-intensity exercise is however delayed compared to MF training.

Trial registration: ClinicalTrials.gov NCT00733941.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological / physiology*
  • Adult
  • Brachial Artery / physiology
  • Echocardiography
  • Exercise / physiology*
  • Female
  • Humans
  • Male
  • Muscle, Skeletal / physiology*
  • Oxygen Consumption / physiology*
  • Respiratory Function Tests
  • Stroke Volume / physiology
  • Treatment Outcome
  • Ventricular Function / physiology*
  • Young Adult

Associated data

  • ClinicalTrials.gov/NCT00733941

Grants and funding

The present study was supported by grants from the K.G. Jebsen Foundation, Norwegian Council of Cardiovascular Disease, The Norwegian Research Council, and Funds for Cardiovascular and Medical Research at St Olav's University Hospital, Trondheim. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.