The purpose of this study was to determine the concurrent validity of a new bench press power (BPP) test using the medicine ball put (MBP) as the criterion measure. Forty-three college-age students (19 males and 24 females) participated in the study. Participants performed 1 repetition at maximum speed using 61.4 kg (males) and 25 kg (females), at a grip width of 130% of biacromial breadth. Timing was initiated manually at the moment of upward bar movement and stopped automatically as the bar broke an infrared beam 0.3 m above the chest. All tests were conducted within 2 weeks. There was 1 practice session for the BPP test and 2 separate testing sessions, one for BPP and the other for the MBP. Three BPP trials were separated by >or=2 minutes of passive recovery. Individual scores were the average of the second and third tests and were expressed in Watts: Power=Bar mass kg.9.81x0.3 m/s. Medicine ball put scores were the average distance the ball was thrown on the second and third trials from a sitting position on a 45 degrees recumbent weight bench. Concurrent validity was determined by conducting a Pearson Correlation on BPP and MBP scores at an alpha level of 0.05: males, r=0.861; females, r=0.79, (p<0.000). In addition, results of an Intraclass R indicated excellent test-retest reliability for both males and females for BPP and the MBP (p<0.05). The conclusion was that the BPP test is a logically and concurrently valid method for coaches and trainers to use in assessing upper body power for both college-age males and females.
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http://dx.doi.org/10.1519/JSC.0b013e3181dad222 | DOI Listing |
Front Pharmacol
January 2025
Department of Emergency Intensive Care Unit, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
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School of Law, Chongqing University, Chongqing, China.
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SingHealth Duke-NUS Breast Centre, Singapore General Hospital, Outram Road 169608 Singapore.
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Mohn Medical Imaging and Visualization Centre (MMIV), Department of Radiology, Haukeland University Hospital, Jonas Lies vei 65, Bergen, 5021, Norway.
Background: Effective diagnostic tools for prompt identification of high-risk locally advanced cervical cancer (LACC) patients are needed to facilitate early, individualized treatment. The aim of this work was to assess temporal changes in tumor radiomics (delta radiomics) from T2-weighted imaging (T2WI) during concurrent chemoradiotherapy (CCRT) in LACC patients, and their association with progression-free survival (PFS). Furthermore, to develop, validate, and compare delta- and pretreatment radiomic signatures for prognostic modeling.
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Design: A cross-sectional survey. The reporting of this study followed the Strengthening the Reporting of Observational Studies in Epidemiology checklist.
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