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临床试验/NCT05216692
NCT05216692已完成不适用

Effects of a Foot Strengthening Protocol on Foot Strength, Foot Morphological Deformation and Kinetics Parameters : a Monocentric Randomized Controlled Trial

François Fourchet2 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2022年1月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
28
试验地点
2
主要终点
Change in Hallux flexion strength

研究概览

简要总结

The principal aim of this study is to investigate the effects of a four-week foot strenghtening protocol combining active voluntary exercises and assisted-active voluntary exercises by neuromuscular electrical stimulation on hallux toe flexion strength in comparison to a standard foot strengthening protocol in a healthy adult recreational active population.

The secondary objectives of the study are to investigate the effects of this protocol on lesser toes flexor strength, foot morphology deformation in one, two and three dimensions and kinetic parameters when walking and running.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Level of weekly physical activity (recreational activity and regular non-competitive runners : at least 1 running session per week)

排除标准

  • History of pain or episodes of foot or ankle sprains during the past 6 months;
  • Foot or leg fractures during the past year;
  • Severe deformity of the foot or leg;
  • Self-declared disability due to neuromuscular impairment of the lower limbs;
  • Neurological or vestibular deficit that could hinder balance (diabetes mellitus, radiculopathie lumbosacral, soft tissue disorder such as Marfan or Ehlers-Danlos syndrome) ;
  • Any absolute contraindication to neuromuscular electrical stimulation (NMES) (cardiac pacemaker, epileptic disorders, pregnancy defibrillator);
  • Participation in an exercise program specifically designed to strengthen the ankle or foot during the last 6 months

结局指标

主要结局

Change in Hallux flexion strength

时间窗: All measures will be collected on both feet 1 week prior the treatment and 1 week after the last intervention session

Hallux flexion strength will be assessed by a MicroFET2 Handheld Digital Dynamometer in hook lying position. The strength will be normalized by bodyweight (N/kg).

次要结局

  • Change in Lesser toe flexion strength(All measures will be collected on both feet 1 week prior the treatment and 1 week after the last intervention session)
  • Change in Running and walking kinetics : Stiffness parameter(All measures will be collected on both feet 1 week prior the treatment and 1 week after the last intervention session)
  • Change in Running and walking kinetics : Pressure parameter(All measures will be collected on both feet 1 week prior the treatment and 1 week after the last intervention session)
  • Change in Running and walking kinetics : Time parameters(All measures will be collected on both feet 1 week prior the treatment and 1 week after the last intervention session)
  • Change in Foot morphological deformation(All measures will be collected on both feet 1 week prior the treatment and 1 week after the last intervention session)
  • Change in Running and walking kinetics : Force parameters(All measures will be collected on both feet 1 week prior the treatment and 1 week after the last intervention session)
  • Change in Running and walking kinetics : Distance parameters(All measures will be collected on both feet 1 week prior the treatment and 1 week after the last intervention session)
  • Change in Running and walking kinetics : Frequency parameter(All measures will be collected on both feet 1 week prior the treatment and 1 week after the last intervention session)

研究者

发起方
François Fourchet
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

François Fourchet

PhD, Physiotherapist. Head of physiotherapy and ergotherapy.

La Tour Hospital

研究点 (2)

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