Introduction: This study assessed the effect of individualized, domain-based exercise intensity prescription on changes in maximal oxygen uptake (V̇O2max) and submaximal thresholds.
Methods: Eighty-four young healthy participants (42 Females, 42 Males) were randomly assigned to six age, sex, and V̇O2max-matched groups (14 participants each). Groups performed continuous cycling in the 1) moderate (MOD)-, 2) lower heavy (HVY1)-, and 3) upper heavy-intensity (HVY2)- domain; interval cycling, in the form of 4) high-intensity interval training (HIIT) in the severe-intensity domain, or 5) sprint-interval training (SIT) in the extreme-intensity domain; or no exercise for, 6) control (CON). All training groups except SIT, were work-matched. Training participants completed three sessions per week for six weeks with physiological evaluations performed at PRE, MID and POST intervention.
Results: Compared to the change in V̇O2max (∆V̇O2max) in CON (0.1 ± 1.2 mL·kg-1·min-1), all training groups except MOD (1.8 ± 2.7 mL·kg-1·min-1), demonstrated a significant increase (p < 0.05). HIIT produced the highest increase (6.2 ± 2.8 mL·kg-1·min-1) followed by HVY2 (5.4 ± 2.3 mL·kg-1·min-1), SIT (4.7 ± 2.3 mL·kg-1·min-1), and HVY1 (3.3 ± 2.4 mL·kg-1·min-1), respectively. The Δ PO at the estimated lactate threshold (θLT) was similar across HVY1, HVY2, HIIT and SIT which were all greater than CON (p < 0.05). The Δ V̇O2 and Δ PO at θLT for MOD was not different from CON (p > 0.05). HIIT produced the highest Δ PO at maximal metabolic steady state, which was greater than CON, MOD, and SIT (p < 0.05).
Conclusions: This study demonstrated that i) exercise intensity is a key component determining changes in V̇O2max and submaximal thresholds and ii) exercise intensity domain-based prescription allows for a homogenous metabolic stimulus across individuals.
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