TY - JOUR
T1 - Comparison of sprint interval and endurance training in team sport athletes
AU - Kelly, David T.
AU - Tobin, Críonna
AU - Egan, Brendan
AU - McCarren, Andrew
AU - O'Connor, Paul L.
AU - Mccaffrey, Noel
AU - Moyna, Niall M.
N1 - Funding Information:
The authors thank Lawrence Spriet, Chris Gerling, and Matt Palmer for their assistance with enzymatic analysis. This research was supported by a research grant from the Gaelic Athletic Association. The results of this study are presented clearly and honestly, without fabrication, falsification, or inappropriate data manipulation and do not constitute endorsement by the authors or the National Strength and Conditioning Association. No conflict of interest, financial or otherwise, is declared by the authors.
Publisher Copyright:
© 2017 NationalStrength and Conditioning Association.
PY - 2018
Y1 - 2018
N2 - High-volume endurance training (ET) has traditionally been used to improve aerobic capacity but is extremely time-consuming in contrast to low-volume short-duration sprint interval training (SIT) that improves maximal oxygen uptake (V O2 max) to a similar extent. Few studies have compared the effects of SIT vs. ET using running-based protocols, or in team sport athletes. Club level male Gaelic football players were randomly assigned to SIT (n = 7; 21.6 ± 2.1 years) or ET (n = 8; 21.9 ± 3.5 years) for ± sessions over 2 weeks. V O2 max, muscle mitochondrial enzyme activity, running economy (RE), and high-intensity endurance capacity (HEC) were measured before and after training. An increase in V O2 max (p ≤ 0.05) after 2 weeks of both SIT and ET was observed. Performance in HEC increased by 31.0 and 17.2% after SIT and ET, respectively (p ≤ 0.05). Running economy assessed at 8, 9, 10, and 11 km·h -1 , lactate threshold and vVO 2 max were unchanged after both SIT and ET. Maximal activity of 3-b-hydroxylacyl coenzyme A dehydrogenase (b-HAD) was increased in response to both SIT and ET (p ≤ 0.05), whereas the maximal activity of citrate synthase remained unchanged after training (p = 0.07). A running-based protocol of SIT is a time-efficient training method for improving aerobic capacity and HEC, and maintaining indices of RE and lactate threshold in team sport athletes.
AB - High-volume endurance training (ET) has traditionally been used to improve aerobic capacity but is extremely time-consuming in contrast to low-volume short-duration sprint interval training (SIT) that improves maximal oxygen uptake (V O2 max) to a similar extent. Few studies have compared the effects of SIT vs. ET using running-based protocols, or in team sport athletes. Club level male Gaelic football players were randomly assigned to SIT (n = 7; 21.6 ± 2.1 years) or ET (n = 8; 21.9 ± 3.5 years) for ± sessions over 2 weeks. V O2 max, muscle mitochondrial enzyme activity, running economy (RE), and high-intensity endurance capacity (HEC) were measured before and after training. An increase in V O2 max (p ≤ 0.05) after 2 weeks of both SIT and ET was observed. Performance in HEC increased by 31.0 and 17.2% after SIT and ET, respectively (p ≤ 0.05). Running economy assessed at 8, 9, 10, and 11 km·h -1 , lactate threshold and vVO 2 max were unchanged after both SIT and ET. Maximal activity of 3-b-hydroxylacyl coenzyme A dehydrogenase (b-HAD) was increased in response to both SIT and ET (p ≤ 0.05), whereas the maximal activity of citrate synthase remained unchanged after training (p = 0.07). A running-based protocol of SIT is a time-efficient training method for improving aerobic capacity and HEC, and maintaining indices of RE and lactate threshold in team sport athletes.
KW - Gaelic football
KW - Maximal oxygen uptake
KW - Mitochondrial enzyme activity
KW - Running
UR - http://www.scopus.com/inward/record.url?scp=85058607256&partnerID=8YFLogxK
U2 - 10.1519/JSC.0000000000002374
DO - 10.1519/JSC.0000000000002374
M3 - Article
C2 - 29373432
AN - SCOPUS:85058607256
SN - 1064-8011
VL - 32
SP - 3051
EP - 3058
JO - Journal of Strength and Conditioning Research
JF - Journal of Strength and Conditioning Research
IS - 11
ER -