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Background: Dancers face significant physical demands and are at high risk for lower extremity injuries due to the complexity and intensity of their movements, which require strong dynamic balance. Improving dynamic balance through training can potentially enhance performance and reduce injury risk.
Objective: This study aimed to investigate the effects of a 12-week combined balance and plyometric training program (BP) compared to plyometric training alone (PL) on dynamic balance and lower extremity injury risk among college dancers.
Methods: A total of 30 female college dancers were randomly assigned to either the BP group (n = 15) or the PL group (n = 15). Both groups participated in a 12-week training program, with the BP group engaging in both balance and plyometric exercises, and the PL group performing only plyometric exercises. Dynamic balance was assessed using the Dynamic Posture Stability Index (DPSI). Lower extremity injury risk was evaluated using the Limb Symmetry Index (LSI) and Center of Pressure (COP) measurements, pre- and post-intervention.
Results: The BP group showed significant improvements in dynamic balance compared to the PL group, with a reduction in DPSI values (DF-DPSI: p < 0.001, partial η = 0.625; DL-DPSI: p < 0.001, partial η = 0.559). Additionally, the BP group showed significant reductions in COP displacements, particularly in the anterior-posterior direction (DF-COPAP: p < 0.015, partial η = 0.101; DL-COPAP: p = 0.019, partial η = 0.094). The BP group also demonstrated greater improvements in LSI-3C and LSI-6, which reflect dynamic stability (LSI-3C: p < 0.001, partial η = 0.229; LSI-6: p = 0.006, partial η = 0.128).
Conclusion: The 12-week combined balance and plyometric training program was more effective than plyometric training alone in improving dynamic balance and reducing lower extremity injury risk in college dancers. This combined training approach is recommended for improving performance and preventing injuries in dancers.
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http://dx.doi.org/10.3389/fphys.2025.1501828 | DOI Listing |
Zhonghua Jie He He Hu Xi Za Zhi
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Center of Drug Metabolism and Pharmacokinetics, China Pharmaceutical University, Nanjing 210009, China. Electronic address:
Prodrugs with enzymatic activation requirements, such as the weakly basic biopharmaceutical classification system (BCS) class IV compound abiraterone acetate (ABA), face considerable bioequivalence (BE) risks owing to their pH-dependent solubility, food effects, and variable intestinal hydrolysis. This study established clinically relevant dissolution specifications for ABA using biorelevant dissolution and physiologically based biopharmaceutics modelling (PBBM). Two dissolution methods, two-stage (gastrointestinal transfer simulation) and single-phase (biorelevant media), were evaluated under fasted and fed conditions.
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