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临床试验/NCT06367790
NCT06367790已完成不适用

Plyometry and Tapping in the Functional Improvement of Non-professional Basketball Players. Randomised Clinical Study

Universidad Católica San Antonio de Murcia1 个研究点 分布在 1 个国家目标入组 19 人开始时间: 2024年4月15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
19
试验地点
1
主要终点
Change from baseline range of motion in loaded dorsal flexion after treatment and at 4 weeks

研究概览

简要总结

Introduction. In basketball, the lower extremities have the highest prevalence of injury, regardless of gender and professional category.

Objective. To analyse the efficacy of a physiotherapy intervention using a protocol of plyometric exercises and dry needling in non-professional basketball athletes.

Methods. Randomised clinical study. 20 players will be randomised to an experimental group (plyometric exercises and dry needling of the gastrocnemius muscles) and a control group (plyometric exercises). The intervention will include 8 sessions over 4 weeks. The study variables will be: range of motion in dorsal flexion in loading (Leg Motion®) and unloading (goniometer) and vertical jump (MyJump2®).

Expected results. An intervention of plyometric exercises and dry needling produces significant differences in range of motion and vertical jump in basketball players, compared to the isolated administration of plyometric exercises.

研究设计

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

入排标准

年龄范围
18 Years 至 30 Years(Adult)
性别
Male
接受健康志愿者
是

入选标准

  • •Non-professional basketball players who are in competition.
  • •Subjects over 18 years of age
  • •Athletes competing in the first men's division of the basketball federation of the Region of Murcia.
  • •Sign the informed consent document.

排除标准

  • •Subjects who are injured at the time of data collection.
  • •Subjects who are unable to attend all training sessions during the duration of the research.
  • •Athletes with apprehension to dry needling.

研究组 & 干预措施

Experimental group

Experimental

The intervention period will last 4 weeks, with a periodicity of 2 weekly sessions of 30 minutes each. All interventions will take place in the sports facilities of both clubs. The interventions will be carried out by the principal investigator of the study. The 10 players assigned to the experimental group will perform plyometric exercises and will undergo dry needling of the gastrocnemius (gastrocnemius muscle) and the control group (plyometric exercises and dry needling of the gastrocnemius muscle).

干预措施: Experimental group (Other)

Control group

Active Comparator

The 10 players assigned to the control group will perform plyometric exercises.

干预措施: Control group (Other)

结局指标

主要结局

Change from baseline range of motion in loaded dorsal flexion after treatment and at 4 weeks

时间窗: Screening visit, within the first seven days after treatment and after four weeks follow-up visit

Loaded dorsiflexion of the ankle will be assessed using the Leg Motion® device. This test consists of placing the athlete barefoot with the foot on the measuring scale of the instrument, requesting maximum knee flexion without lifting the heel. The test is performed 3 times and the average value is used in the data analysis. The unit of measurement is the maximum distance, measured in centimetres, between the toe and the metal bar. The greater the distance, the greater the dorsiflexion in ankle loading.

次要结局

  • Change from baseline vertical jump after treatment and at 4 weeks(Screening visit, within the first seven days after treatment and after four weeks follow-up visit)
  • Change from baseline range of motion in unloaded dorsal flexion after treatment and at 4 weeks(Screening visit, within the first seven days after treatment and after four weeks 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

Principal Investigator

Universidad Católica San Antonio de Murcia

研究点 (1)

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