Study Design: Randomized clinical trial.
Objectives: To investigate the clinical efficacy of the addition of the Protonics system to a standard exercise-based patellofemoral rehabilitation protocol.
Background: The Protonics system has been suggested as an intervention for patients with patellofemoral pain syndrome (PFPS). However, the effects of this system have not been compared to the effects associated with traditional exercise-based rehabilitation alone.
Methods And Measures: Seventeen of 34 females (mean age, 28 years; range, 13-55 years) diagnosed with PFPS were randomly assigned to wear the Protonics system while participating in a conventional exercise-based rehabilitation program. Functional and patient-reported outcome measures were evaluated, including Kujala score and the lateral step-up test. In addition, measurements of hip internal and external rotation, hip extension, and iliotibial band muscle length were compared between groups.
Results: Patients in both groups demonstrated improvement in Kujala score (P<.001), performance on the lateral step-up test (P<.001), and pain during the step-up test (P<.001) at the conclusion of the study. However, there was no difference between groups with respect to improvement in Kujala score (P = .33), step-up test performance (P = .47), or pain during the step-up test (P = .24). Patients using the Protonics system demonstrated greater gain in passive hip extension (P = .023) and increased hip external rotation motion (P = .017) at discharge versus patients treated with exercise alone. However, there was no difference in iliotibial band flexibility (P = .80) or hip internal rotation motion (P = .09) between groups. A greater proportion of patients in the Protonics group reported no pain with step-up testing at each 2-week interval. However, the 2.2 fewer visits required by patients in the Protonics group to meet discharge criteria did not achieve statistical significance (P = .08).
Conclusions: Patients using the Protonics system demonstrated a shift in available hip rotation and increased passive hip extension flexibility. However, these changes were not outside the bounds of potential measurement error and did not translate into significant functional differences from a similar group treated with exercise alone. The economic implications of an average 2.2-visit decrease in treatment sessions per patient using the Protonics system are uncertain.
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http://dx.doi.org/10.2519/jospt.2005.35.4.210 | DOI Listing |
J Am Chem Soc
January 2025
State Key Laboratory of Catalysis, Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, PR China.
A prevalent challenge in particulate photocatalytic water splitting lies in the fact that while numerous photocatalysts exhibit outstanding hydrogen evolution reaction (HER) activity in organic sacrificial reagents, their performance diminishes markedly in a Z-scheme water splitting system using electronic mediators. This underlying reason remains undefined, posing a long-standing issue in photocatalytic water splitting. Herein, we unveiled that the primary reason for the decreased HER activity in electronic mediators is due to the strong adsorption of shuttle ions on cocatalyst surfaces, which inhibits the initial proton reduction and results in a severe backward reaction of the oxidized shuttle ions.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Politecnico di Torino, Corso Duca degli Abruzzi 24, 10129, Torino, ITALY.
Ammonia electrosynthesis through the lithium-mediated approach has recently reached promising results towards high activity and selectivity in aprotic media, reaching high Faradaic efficiency (FE) values and NH3 production rates. To fasten the comprehension and optimization of the complex lithium-mediated nitrogen reduction system, for the first time a multivariate approach is proposed as a powerful tool to reduce the number of experiments in comparison with the classical one-factor-at-a-time approach. Doehlert design and surface response methodology are employed to optimize the electrolyte composition for a batch autoclaved cell.
View Article and Find Full Text PDFMetal oxides are promising catalysts for small molecule hydrogen chemistries, mediated by interfacial proton-coupled electron transfer (PCET) processes. Engineering the mechanism of PCET has been shown to control the selectivity of reduced products, providing an additional route for improving reductive catalysis with metal oxides. In this work, we present kinetic resolution of the rate determining proton-transfer step of PCET to a titanium-doped POV, TiVO(OCH) with 9,10-dihydrophenazine by monitoring the loss of the cationic radical intermediate using stopped-flow analysis.
View Article and Find Full Text PDFChemistry
January 2025
University of Oxford, Inorganic Chemistry Laboratory, UNITED KINGDOM OF GREAT BRITAIN AND NORTHERN IRELAND.
Combining experiment and theory, the mechanisms of H2 activation by the potassium-bridged aluminyl dimer K2[Al(NON)]2 (NON = 4,5-bis(2,6-diisopropylanilido)-2,7-di-tertbutyl-9,9-dimethylxanthene) and its monomeric K+-sequestered counterpart have been investigated. These systems show diverging reactivity towards the activation of dihydrogen, with the dimeric species undergoing formal oxidative addition of H2 at each Al centre under ambient conditions, and the monomer proving to be inert to dihydrogen addition. Noting that this K+ dependence is inconsistent with classical models of single-centre reactivity for carbene-like Al(I) species, we rationalize these observations instead by a cooperative frustrated Lewis pair (FLP)-type mechanism (for the dimer) in which the aluminium centre acts as the Lewis base and the K+ centres as Lewis acids.
View Article and Find Full Text PDFSci China Life Sci
January 2025
The Key Laboratory of Medical Molecular Cell Biology of Shanxi Province, Institutes of Biomedical Sciences, Shanxi University, Taiyuan, 030006, China.
The cGAS-STING pathway plays a crucial role in the innate immune system by detecting mislocalized double-stranded DNA (dsDNA) in the cytoplasm and triggering downstream signal transduction. Understanding the mechanisms by which cGAS and STING operate is vital for gaining insights into the biology of this pathway. This review provides a detailed examination of the structural features of cGAS and STING proteins, with a particular emphasis on their activation and inhibition mechanisms.
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