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首页> 外文期刊>Disability and rehabilitation. >Efficacy of custom-fitted footwear to increase physical activity in children and adolescents with Down syndrome (ShoeFIT): randomised pilot study
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Efficacy of custom-fitted footwear to increase physical activity in children and adolescents with Down syndrome (ShoeFIT): randomised pilot study

机译:定制鞋类对综合征(Shoefit)增加儿童和青少年体育活动的疗效(Shoefit):随机试验研究

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Purpose: To determine the feasibility of conducting a definitive randomised trial to evaluate the efficacy of custom-fitted footwear for increasing physical activity in children and adolescents with Down syndrome. Methods: Assessor-blinded, parallel-group randomised pilot study. Thirty-three children and adolescents with Down syndrome were randomly allocated to a custom-fitted footwear group (Clarks (R) footwear) or a wait-list control group. Six feasibility domains were evaluated at baseline, 6 and 12 weeks; demand (recruitment), implementation (co-interventions and adherence), acceptability, practicality (adverse events), limited efficacy testing (physical activity, disability associated with foot and ankle problems, and gait parameters), and adaptation (shoe-fit). Results: Three participants were recruited per month. The use of co-interventions was common with six control group participants purchasing new footwear during the study. Mean adherence was 35 h/week in the custom-fitted footwear group, and there were few minor adverse events. There were trends for differences in physical activity favouring the custom-fitted footwear, but no trends for differences in disability associated with foot and ankle problems or gait parameters. The fit of the custom-fitted footwear was no better than participants' regular footwear. Conclusions: A definitive randomised trial is feasible. However, recruitment, use of co-interventions and footwear fit need further consideration.
机译:目的:确定进行最终随机试验的可行性,以评估定制鞋类对唐氏综合征儿童和青少年增加体力活动的效果。方法:评估员盲法、平行组随机试验研究。33名患有唐氏综合征的儿童和青少年被随机分配到定制鞋类组(Clarks(R)鞋类)或等待名单对照组。在基线检查、6周和12周时评估了六个可行性领域;需求(招募)、实施(联合干预和依从性)、可接受性、实用性(不良事件)、有限功效测试(体力活动、与足部和脚踝问题相关的残疾、步态参数)和适应(鞋子合脚)。结果:每月招募三名参与者。在研究期间,共有六名对照组参与者购买了新鞋,这是共同干预的常见做法。定制鞋组的平均坚持时间为35小时/周,几乎没有轻微的不良事件。有倾向于定制合脚鞋的体力活动差异的趋势,但没有与脚和脚踝问题或步态参数相关的残疾差异的趋势。定制合脚鞋的合脚性并不比参与者的普通鞋好。结论:明确的随机试验是可行的。然而,招募、联合干预的使用和鞋子的合脚需要进一步考虑。

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