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首页> 外文期刊>Trials >Protocol, and practical challenges, for a randomised controlled trial comparing the impact of high intensity interval training against standard care before major abdominal surgery: study protocol for a randomised controlled trial
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Protocol, and practical challenges, for a randomised controlled trial comparing the impact of high intensity interval training against standard care before major abdominal surgery: study protocol for a randomised controlled trial

机译:关于随机对照试验的议定书和实际挑战,比较高强度间隔训练对主要腹部手术前的标准护理的影响:用于随机对照试验的研究方案

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Risk factors, such as the number of pre-existing co-morbidities, the extent of the underlying pathology and the magnitude of the required operation, cannot be changed before surgery. It may, however, be possible to improve the cardiopulmonary fitness of the patient with an individualised exercise program. We are performing a randomised controlled trial (RCT) assessing the impact of High Intensity Interval Training (HIIT) on preoperative cardiopulmonary fitness and postoperative outcomes in patients undergoing major abdominal surgery. Consecutive eligible patients undergoing elective abdominal surgery are being randomised to HIIT or standard care in a 1:1 ratio. Participants allocated to HIIT will perform 14 exercise sessions on a stationary cycle ergometer, over a period of 4-6 weeks before surgery. The sessions, which are individualised, aim to start with ten repeated 1-min blocks of intense exercise with a target of reaching a heart rate exceeding 90% of the age predicted maximum, followed by 1 min of lower intensity cycling. As endurance improves, the duration of exercise is increased to achieve five 2-min intervals of high intensity exercise followed by 2 min of lower intensity cycling. Each training session lasts approximately 30?min. The primary endpoint, change in peak oxygen consumption (Peak VO2) measured during cardiopulmonary exercise testing, is assessed at baseline and before surgery. Secondary endpoints include postoperative complications, length of hospital stay and three clinically validated scores: the surgical recovery scale; the postoperative morbidity survey; and the SF-36 quality of life score. The standard deviation for changes in Peak VO2 will be assessed after the first 30 patients and will be used to calculate the required sample size. We want to assess if 14 sessions of HIIT is sufficient to improve Peak VO2 by 2?mL/kg/min in patients undergoing major abdominal surgery and to explore the best clinical endpoint for a subsequent RCT designed to assess if improving Peak VO2 will translate into improving clinical outcomes after surgery. Australian New Zealand Clinical Trials Registry, ACTRN12617000587303 . Registered on 26 April 2017.
机译:危险因素,例如预先存在的共同状况,潜在病理的程度以及所需操作的程度,不能在手术前改变。然而,它可以通过个性化的锻炼计划改善患者的心肺含量。我们正在进行一项随机对照试验(RCT),评估高强度间隔训练(HIIT)对术前心肺健身和术后腹部手术患者术后结果的影响。接受选修腹部手术的连续符合条件的患者正在1:1的比例随机分配到HIIT或标准护理。分配给Hiit的参与者将在手术前4-6周的4-6周内进行14位运动课程。个性化的会话旨在从十个重复的1分钟的强烈运动块,其目标达到超过最大年龄的90%的心率,然后较低强度循环。随着耐久性的改善,锻炼的持续时间增加以达到高强度锻炼的五个2分钟间隔,然后进行2分钟的较低强度循环。每个培训课程持续大约30?分钟。在基线和手术前评估了在心肺运动测试期间测量的峰值氧消耗(峰值VO2)的初级终点(峰值VO2)。次要终点包括术后并发症,医院住宿时间和三个临床验证的分数:外科恢复量表;术后发病率调查;和SF-36生活质量得分。在前30名患者之后,将评估峰值VO2变化的标准偏差,并将用于计算所需的样品尺寸。我们希望评估14个HIIT的会话是否足以在接受主要腹部手术的患者中提高2?ml / kg / min的峰值VO2,并探索旨在评估改善峰值VO2的后续RCT的最佳临床终点,如果改善峰值VO2将转化为提高手术后的临床结果。澳大利亚新西兰临床试验登记处,ACTRN12617000587303。 2017年4月26日注册。

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