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首页> 外文期刊>Pilot and Feasibility Studies >Unsupervised progressive elastic band exercises for frail geriatric inpatients objectively monitored by new exercise-integrated technology—a feasibility trial with an embedded qualitative study
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Unsupervised progressive elastic band exercises for frail geriatric inpatients objectively monitored by new exercise-integrated technology—a feasibility trial with an embedded qualitative study

机译:通过新的运动集成技术客观地监测脆弱的老年患者的无监督渐进式弹性带运动-一项具有嵌入式定性研究的可行性试验

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Frailty is a serious condition frequently present in geriatric inpatients that potentially causes serious adverse events. Strength training is acknowledged as a means of preventing or delaying frailty and loss of function in these patients. However, limited hospital resources challenge the amount of supervised training, and unsupervised training could possibly supplement supervised training thereby increasing the total exercise dose during admission. A new valid and reliable technology, the BandCizer, objectively measures the exact training dosage performed. The purpose was to investigate feasibility and acceptability of an unsupervised progressive strength training intervention monitored by BandCizer for frail geriatric inpatients.MethodsThis feasibility trial included 15 frail inpatients at a geriatric ward. At hospitalization, the patients were prescribed two elastic band exercises to be performed unsupervised once daily. A BandCizer Datalogger enabling measurement of the number of sets, repetitions, and time-under-tension was attached to the elastic band. The patients were instructed in performing strength training: 3 sets of 10 repetitions (10–12 repetition maximum (RM)) with a separation of 2-min pauses and a time-under-tension of 8?s. The feasibility criterion for the unsupervised progressive exercises was that 33% of the recommended number of sets would be performed by at least 30% of patients. In addition, patients and staff were interviewed about their experiences with the intervention.ResultsFour (27%) out of 15 patients completed 33% of the recommended number of sets. For the total sample, the average percent of performed sets was 23% and for those who actually trained ( n ?=?12) 26%. Patients and staff expressed a general positive attitude towards the unsupervised training as an addition to the supervised training sessions. However, barriers were also described—especially constant interruptions.ConclusionsBased on the predefined criterion for feasibility, the unsupervised training was not feasible, although the criterion was almost met. The patients and staff mainly expressed positive attitudes towards the unsupervised training. As even a small training dosage has been shown to improve the physical performance of geriatric inpatients, the proposed intervention might be relevant if the interruptions are decreased in future large-scale trials and if the adherence is increased.Trial registrationClinicalTrials.gov: NCT02702557, February 29, 2016. Data Protection Agency: 2016-42, February 25, 2016. Ethics Committee: No registration needed, December 8, 2015 (e-mail correspondence).
机译:衰弱是老年患者中经常出现的严重状况,有可能引起严重的不良事件。力量训练被认为是预防或延迟这些患者的虚弱和功能丧失的一种手段。但是,有限的医院资源挑战了有监督训练的数量,无监督训练可能会补充有监督训练,从而增加入院期间的总运动剂量。一种新的有效可靠的技术BandCizer可客观地测量执行的精确训练剂量。目的是研究由BandCizer监测的无监督渐进式力量训练干预措施对脆弱的老年患者的可行性和可接受性。方法该可行性试验包括15位在老年病房的脆弱患者。在住院期间,为患者开了两次橡皮筋运动,每天不带监督地进行一次。松紧带上装有一个BandCizer数据记录仪,该记录仪可测量套数,重复次数和拉紧时间。指导患者进行力量训练:3组,每组10次重复(最大10–12次重复(RM)),间隔2分钟,间歇时间为8?s。无监督进行性锻炼的可行性标准是,至少30%的患者应进行33%的推荐套数练习。此外,还对患者和工作人员进行了干预的经历进行了采访。结果15例患者中有4例(27%)完成了建议套数的33%。对于总样本,执行组的平均百分比为23%,而对于实际训练过的样本(n = 12),则为26%。病人和工作人员对无监督培训表示普遍的积极态度,这是对有监督培训的补充。但是,还描述了障碍,尤其是持续不断的中断。结论基于可行性的预定义标准,尽管几乎满足该标准,但无监督的训练也不可行。患者和医护人员主要对无监督的培训表示积极的态度。由于即使是很小的训练剂量也能改善老年患者的身体表现,因此,如果在以后的大规模试验中减少干扰并增加依从性,则建议的干预措施可能是有意义的。ClinicalTrials.gov:NCT02702557,2月2016年2月29日。数据保护局:2016-42,2016年2月25日。职业道德委员会:无需注册,2015年12月8日(电子邮件通信)。

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