2018
DOI: 10.1007/978-3-030-01845-0_7
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Clinical Benefits and Acceptability of Two Commercial Arm Exoskeletons for Patients with Muscular Dystrophy

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Cited by 6 publications
(9 citation statements)
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“…However, even if a remarkable number of works have been published dealing with the development of innovative electromechanical technologies (e.g., Ragonesi et al, 2013;Jung et al, 2014;Dunning et al, 2015;Sin et al, 2015;Dalla Gasperina et al, 2018), scientific evidence for the benefits of these technologies is still lacking, which could justify costs and effort. When dealing with Assistive Devices, or in general with complex technologies, the demonstration of the effectiveness of their use is rather difficult to be demonstrated following the canonical research studies design [i.e., Randomized Control Trial (RCT) design], even if some effort in this direction is currently ongoing (Antonietti et al, 2019). This is due to several reasons, such as the difficulty to demonstrate the validity of the proposed approach independently from the users' placebo effect (e.g., it is impossible to perform a blind session), the high cost of the technology and therefore the impossibility to recruit many volunteers contemporary, and the Ethical Committee procedures for non CE-marked devices.…”
Section: Introductionmentioning
confidence: 99%
“…However, even if a remarkable number of works have been published dealing with the development of innovative electromechanical technologies (e.g., Ragonesi et al, 2013;Jung et al, 2014;Dunning et al, 2015;Sin et al, 2015;Dalla Gasperina et al, 2018), scientific evidence for the benefits of these technologies is still lacking, which could justify costs and effort. When dealing with Assistive Devices, or in general with complex technologies, the demonstration of the effectiveness of their use is rather difficult to be demonstrated following the canonical research studies design [i.e., Randomized Control Trial (RCT) design], even if some effort in this direction is currently ongoing (Antonietti et al, 2019). This is due to several reasons, such as the difficulty to demonstrate the validity of the proposed approach independently from the users' placebo effect (e.g., it is impossible to perform a blind session), the high cost of the technology and therefore the impossibility to recruit many volunteers contemporary, and the Ethical Committee procedures for non CE-marked devices.…”
Section: Introductionmentioning
confidence: 99%
“…58.9 ± 54.1% [2] 6.5 ± 17.0% [3] 65.3 ± 48.8% [4] 67.5 ± 33.4% [5] 15 ± 15.7% [6] 12.4 ± 10.3% [7] 22.0 ± 23.8% [8] 7.7 ± 21.8% [10] 18 ± 34.4% [11] 19.5 ± 10.8% [12] 13.2 ± 10.8% [13] 10.8 ± 44.2% [14] 5.0 ± 22.7% [15] 37.4 ± 19.9% [16] 29.6 ± 21.7% [17] 23.8 ± 46.1% Table 1. Percentage improvement in the performances (∆Perf) measured with the AD with respect to the performances without the AD (mean ± standard deviation).…”
Section: Assistive Device Effectsmentioning
confidence: 99%
“…All included studies compared patients' ability to perform functional tasks with and without ADs. Most of the studies (11) included at least one subject affected by MD, involving overall 73 MD subjects [6,15,16,13,4,8,11,17,10,2,5], while 3 studies included 33 stroke subjects [12,7,14], one study included 3 SCI patients [1], and another study included 4 MS patients [3].…”
Section: Identified Studiesmentioning
confidence: 99%
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