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Design of an eccentric recumbent ergometer to elicit delayed onset muscle soreness. 设计一种偏心式腰部测力计,以诱发迟发性肌肉酸痛。
Pub Date : 2021-01-01 Epub Date: 2021-04-15
Sara A Harper, Frederick J Peters, Brandon S Pollock, Keith Burns, John McDaniel, Angela L Ridgel

Introduction: Our objective was to design an eccentric bicycle design to elicit delayed onset muscle soreness (DOMS).

Methods: To assess the bicycle designs' ability to elicit DOMS, fourteen, recreationally active, males performed five-minutes of eccentric bicycling at 50% of their individualized power determined from a modified six-second Wingate test. Outcome measures to assess DOMS included the Likert pain scale, creatine kinase, lactate blood concentration, and pressure algometry detection evaluated at four time points (baseline (before the eccentric bicycling), immediate post, 24 hours post, and 48 hours post).

Results: The Likert pain scale was different (F = 75.88, p < 0.001) at baseline (0.14 ± 0.36) and immediate post (0.21 ± 0.43), compared to 24 hours post (3.07 ± 0.83), and 48 hours post (2.93 ± 1.07). No changes were reported for creatine kinase (F = 0.7167, p = 0.475), lactate blood concentration (F = 2.313, p = 0.107), or pressure algometry detection.

Conclusions: To understand mechanisms of DOMS, there is a need for a consistent, reliable method for producing DOMS. Our eccentric bicycle design and protocol offers an alternative approach to previous eccentric ergometer designs - demonstrating the potential to elicit DOMS in one, five-minute session.

简介:我们的目的是设计一种偏心自行车,以引起延迟性肌肉酸痛(DOMS):我们的目的是设计一种偏心自行车,以引起延迟性肌肉酸痛(DOMS):为了评估自行车设计引起 DOMS 的能力,14 名从事娱乐活动的男性在改良的六秒 Wingate 测试中,以 50%的个人化力量进行了五分钟的偏心自行车运动。评估 DOMS 的结果指标包括李克特疼痛量表、肌酸激酶、乳酸血液浓度以及在四个时间点(基线(偏心骑车前)、刚骑车后、骑车后 24 小时和骑车后 48 小时)进行的压力算法检测:李克特疼痛量表在基线(0.14 ± 0.36)和刚开始时(0.21 ± 0.43)与 24 小时后(3.07 ± 0.83)和 48 小时后(2.93 ± 1.07)之间存在差异(F = 75.88,p < 0.001)。肌酸激酶(F = 0.7167,P = 0.475)、乳酸血液浓度(F = 2.313,P = 0.107)或压力算法检测均无变化:为了了解 DOMS 的机制,需要一种一致、可靠的方法来产生 DOMS。我们的偏心自行车设计和方案提供了一种替代以往偏心测力计设计的方法--证明了在一次五分钟的训练中激发 DOMS 的潜力。
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引用次数: 0
The Validity of a Novel Low-Cost, Wearable Physical Activity Monitor in a Laboratory Setting 一种新型低成本、可穿戴式运动监测仪在实验室环境中的有效性
Pub Date : 2017-05-01 DOI: 10.1249/01.mss.0000519036.63655.29
A. Newton, E. Glickman, Curtis Fennell, J. Gunstad, Jacob E. Barkley
Introduction: Wearable physical activity monitors are popular and may provide a more accurate data than subjective methods. The present study assessed the validity of a novel, low-cost wearable physical activity monitor (Movband 3) relative to established measures.Methods: Participants (N = 19) completed four treadmill stages (1.5, 3.0, 4.0, 6.0 MPH) while wearing the Movband 3 and the validated Actigraph GT1M monitor. Oxygen consumption (VO2 ml/kg/min) and heart rate (beats/min) were recorded. The relationship between Movband data and established measures was assessed via Pearson’s correlations. Tests of agreement were performed for actual and Movband miles traveled.  Results: There were large, positive, significant (p < 0.001) effect sizes for the associations between Movband counts and Actigraph counts (r = 0.72), VO2 (r = 0.59), and heart rate (r = 0.63). There was also a large, positive, significant (p < 0.001) association between actual and Movband miles (r = 0.97). However, the difference (Δ) between Movband and actual miles was greater than a null hypothesis of zero (∆ = 0.77 ± 0.45 miles or 31.8%, t = 7.4, p < 0.001).Conclusion: While there was evidence to support the validity of the Movband 3 for the assessment of physical activity intensity this device did not provide an accurate measure of miles traveled.  
简介:可佩戴的身体活动监测仪很受欢迎,它可能比主观方法提供更准确的数据。本研究评估了一种新型低成本可穿戴身体活动监测仪(Movband 3)相对于既定测量的有效性。方法:参与者(N=19)在佩戴Movband 3和经验证的Actigraph GT1M监测仪的情况下完成了四个跑步机阶段(1.5、3.0、4.0、6.0 MPH)。记录耗氧量(VO2ml/kg/min)和心率(次/分)。通过Pearson相关性评估了Movb与数据和既定测量之间的关系。对实际行驶里程和Movband行驶里程进行了一致性测试。结果:Movband计数与Actigraph计数(r=0.72)、VO2(r=0.59)和心率(r=0.63)之间的相关性存在较大的、积极的、显著的(p<0.001)效应大小。实际值与Movband英里数之间也存在较大的正性、显著的相关性(r=0.97)。然而,Movband和实际里程之间的差异(Δ)大于零的零假设(∆=0.77±0.45英里或31.8%,t=7.4,p<0.001)。
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Research Directs in health sciences
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