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临床试验/NCT06894537
NCT06894537已完成不适用

Efficacy of Echo-guided Percutaneous Electrical Nerve Stimulation of the Femoral Nerve on Explosive Strength and Metabolic Response in Healthy Subjects. A Randomised Clinical Trial.

Universidad Católica San Antonio de Murcia1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2025年3月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
32
试验地点
1
主要终点
Change from baseline jump height after warming, treatment and at 1 and 24 hours

研究概览

简要总结

Introduction. Variables such as pain and strength can be modified in the short and medium term by the application of currents. The percutaneous form of percutaneous needle-guided acupuncture can eliminate the impedance of the surrounding tissues that limit the optimal diffusion of the current to the target tissue. It is necessary to objectify the metabolic response of this technique and its effects in terms of strength and metabolic response.

Objective. To evaluate the safety and efficacy, in acute and subacute phases, of percutaneous electrical nerve stimulation in healthy subjects.

Method. Single-blind randomised clinical study. Thirty-two subjects will be recruited and randomised to the experimental and control groups. The intervention in the experimental group will consist of a percutaneous percutaneous electrical nerve stimulation of the femoral nerve, while in the control group the same intervention will be performed without increasing the intensity of the current. The primary variable will be vertical jump height (My Jump® iOS app) and the secondary variable will be skin temperature (Hikmicro M60 model Hangzhou).

研究设计

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

入排标准

年龄范围
18 Years 至 24 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Persons aged 18 and
  • •Of both sexes.
  • •Who practice sport at least twice a week.
  • •Who sign the informed consent document.

排除标准

  • •Medical diagnosis of chronic systemic diseases or diseases that may interfere with thermographic imaging (rheumatoid arthritis, fibromyalgia, deep vein thrombosis, etc.).
  • •Having undergone lower limb surgery in the 24 months prior to the study.
  • •Intake of drugs that may influence the thermographic response (antipyretics, non-steroidal anti-inflammatory drugs, topical solutions on the area to be studied, etc.).
  • •People with nickel allergy or belonephobia (needle phobia).

研究组 & 干预措施

Experimental group

Experimental

The intervention of the experimental group will consist of an intervention by performing percutaneous echo-guided electrical nerve stimulation of the femoral nerve.

干预措施: Experimental (percutaneous echo-guided electrical nerve stimulation) (Other)

Control

Active Comparator

The intervention of the control group will be carried out in the same way as in the experimental intervention, but without increasing the intensity of the current.

干预措施: Control (placebo) group (Other)

结局指标

主要结局

Change from baseline jump height after warming, treatment and at 1 and 24 hours

时间窗: Baseline, within the first seven days after warming, treatment and after 1 and 24 hours follow-up visit

Using the My Jump® application (iOS app), the jump height is evaluated. This tool measures the time in the air (in milliseconds), indirectly assessing the height of the jump (in centimetres). This tool has shown a high reliability in the evaluation of counter movement jump. The unit of measurement is centimetres (cm), where the higher the centimetres, the higher the jump height.

次要结局

  • Change from baseline muscle power after warming, treatment and at 1 and 24 hours(Baseline, within the first seven days after warming, treatment and after 1 and 24 hours follow-up visit)

研究者

发起方
Universidad Católica San Antonio de Murcia
申办方类型
Other
责任方
Principal Investigator
主要研究者

Rubén Cuesta-Barriuso, PhD

PhD

Universidad Católica San Antonio de Murcia

研究点 (1)

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