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临床试验/NCT06766318
NCT06766318已完成不适用

Cryo-ultrasound Versus LASER Therapy on Ankle Sprain in Tennis Players

October 6 University2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年2月9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
入组人数
40
试验地点
2
主要终点
Pain intensity a

研究概览

简要总结

the effect cryo-ultrasound therapy and LASER therapy on the short-term recovery of tennis players with acute lateral ankle sprains.

详细描述

Acute lateral ankle sprains are common injuries among athletes, but the optimal treatment strategies in elite athletes are still debated. This proof-of-concept study aimed to assess the impact of cryo-ultrasound therapy and LASER therapy on the short-term recovery of tennis players with acute lateral ankle sprains.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Other
盲法
Double (Participant, Investigator)

入排标准

年龄范围
12 Years 至 16 Years(Child)
性别
Female
接受健康志愿者
否

入选标准

  • •Age ranged from 12-16 years.
  • •elite girls;
  • •semi-professional tennis players;
  • •I-II grade lateral ankle sprain injury;
  • •no persistent instability phenomena or chronic sprains;
  • •acute injury (within 2 weeks from trauma);
  • •no evidence of bone edema or skin disorder, once the area of intense pain in motion was delimited, the lack of neurological disturbances was investigated and assessed.

排除标准

  • •history of recurrent dislocation of the ankle or hyperlaxity of any joint;
  • •severe rheumatic diseases and/or collagen diseases;
  • •athletes who have received any form of local physical therapy and NSAIDs within the last 2 months prior to injury;
  • •athletes who admit to using steroids;
  • •any contraindication and/or limitation to the use of a physical agent modality (implantable electrophysiological devices, active neoplasms). Taking medications.
  • •Athletic adult.

研究组 & 干预措施

cryo-ultrasound group (n = 20): received cryo-ultrasound therapy

Experimental

received cryo-ultrasound therapy combined with conventional physical therapy

干预措施: group A will receive cryo-ultrasound therapy combined with conventional physical therapy for two months (Device)

Laser group

Experimental

receive LASER therapy combined with conventional physical therapy

干预措施: LASER therapy (Device)

结局指标

主要结局

Pain intensity a

时间窗: 2 months

We will assess pain intensity before and after intervension by numeric pain rating scale, which is numerical from 0 indicate no pain and 10 indicate the worest pain

Foot and Ankle Disability Index

时间窗: 2 months

Foot and Ankle Disability Index (FADI) at baseline (T0) at the end of treatment (T1), after one month (T2), and two months after treatment (T3).

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kerolous Ishak Shehata

Assistant professor

October 6 University

研究点 (2)

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