The Ability of a Submaximal Cycle Ergometer Test to Detect Longitudinal Changes in VO2Max

Background: The purpose of the present study was to examine the ability of a submaximal cycling test to detect longitudinal changes in maximal oxygen uptake (VO 2 max) and examine the conformity between changes in measured and estimated VO 2 max over a time span of 5–8 years. Methods A total of 35 participants (21 men and 14 women), aged 29 to 63 years, performed the Ekblom-Bak (EB) submaximal cycle test for estimation of VO 2 max and a maximal treadmill running test for direct measurement of VO 2 max. The baseline tests were conducted between 2009 and 2012, and the follow-up tests were completed 5 to 8 years later. Pearson’s coefficient of correlation ( r ) and paired sample t- test were used to analyse the association between change in measured and estimated VO 2 max. Random and systematic errors between the measured and estimated VO 2 max were evaluated using Bland-Altman plots. Repeated measures ANOVA were used to test differences between changes over time. Results There was no significant change in mean measured VO 2 max between baseline and follow-up ( p  = 0.91), however large individual variations were noted (-0.78 to 0.61 L/min). The correlation between individual change in measured and estimated VO 2 max was r  = 0.75 ( p  < 0.05), and the unstandardised B-coefficient from linear regression modelling was 0.88 (95% CI: 0.61 to 1.15), i.e. , for each litre of change in estimated VO 2 max, the measured value had changed 0.88 L. The correlation between baseline and follow-up errors (the difference between estimated-measured VO 2 max at each occasion) was r  = 0.84 ( p  < 0.05). With regard to the testing procedure, repeated measures ANOVA revealed that there was no significant difference between the group who exercised at the same work rates at baseline and follow-up (n = 25), and those who required a change in work rate (n = 10). Conclusion The EB test detected a change in VO 2 max with reasonably good precision over a time span of 5–8 years. Further studies are needed to evaluate if the test can be used in clinical populations and in subjects with different medications.