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临床试验/NCT05093985
NCT05093985Unknown不适用

Investigating the Effect of Neuromuscular Electrical Stimulation and Blood Flow Restriction Training on Physiological Deconditioning During Unloading and Retraining

St Mary's University College0 个研究点目标入组 36 人开始时间: 2021年11月15日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
36
主要终点
Change in maximal isometric strength via Biodex Dynamometer

研究概览

简要总结

Following injury or surgery to a limb, it is often immobilised to allow tissue healing. Short periods of disuse cause loss of muscle size and strength and impaired mechanical properties of tendons, which leads to reduced function. Strategies to combat these deconditioning adaptations include neuromuscular electrical stimulation (NMES), however at present its effectiveness is limited. Recent research suggests that the effects of NMES can be augmented with blood flow restriction (BFR). At present, the effect of combining these two techniques on muscle function during limb immobilisation is unknown. Furthermore, the impact of BFR training during retraining following immobilisation is unknown.

详细描述

Following injury or surgery to a limb, it is often immobilised to allow tissue healing. Short periods of disuse cause loss of muscle size and strength and impaired mechanical properties of tendons, which leads to reduced function. Strategies to combat these deconditioning adaptations include neuromuscular electrical stimulation (NMES), however at present its effectiveness is limited. Recent research suggests that the effects of NMES can be augmented with blood flow restriction (BFR). At present, the effect of combining these two techniques on muscle function during limb immobilisation is unknown. Furthermore, the impact of BFR training during retraining following immobilisation is unknown.

This study will examine the effectiveness and feasibility of a neuromuscular electrical stimulation and blood flow restriction protocol during a 7 day period of immobilisation. Multiple measures across several physiological systems will be obtained.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Between the age of 18-55
  • Non-smoker
  • No previous history of cardiovascular, respiratory or neurological problems
  • Not taking anticoagulant medication
  • Injury-free in the 3 months prior to scheduled participation in the study.

排除标准

  • Hypertension (<140/80)
  • Metal work in-situ
  • Blood diseases or clotting issues
  • Injury or previous injury (<3 months prior to scheduled participation in the study)
  • Pregnancy

结局指标

主要结局

Change in maximal isometric strength via Biodex Dynamometer

时间窗: Through study completion, an average of 1 year

Strength measure

Change in maximal isokinetic strength via Biodex Dynamometer

时间窗: Through study completion, an average of 1 year

Strength measure

次要结局

  • Change in muscle VO2 via near-infrared spectroscopy(Through study completion, an average of 1 year)
  • Change in blood markers via venous blood samples(Through study completion, an average of 1 year)
  • Change in muscle endurance via Biodex Dynamometer(Through study completion, an average of 1 year)
  • Change in muscle morphology via 2D and 3D ultrasonography(Through study completion, an average of 1 year)
  • Change in pressure pain thresholds via handheld allometry(Through study completion, an average of 1 year)
  • Change in corticomotor excitability and inhibition, via transcranial magnetic stimulation(Through study completion, an average of 1 year)

研究者

发起方
St Mary's University College
申办方类型
Other
责任方
Sponsor

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