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临床试验/CTRI/2024/01/061714
CTRI/2024/01/061714尚未招募3 期

Efficacy Of Dry Needling In The Management Of Achilles Tendinopathy In Basketball Players

NITISH KUMAR SRIVASTAVA1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年2月1日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
1. VAS,

研究概览

简要总结

This study holds substantial clinical significance as it addresses a critical gap in the current literature regarding the efficacy of dry needling in managing Achilles tendinopathy specifically within the basketball player population. By providing valuable insights into the potential benefits of this intervention, the findings from this research could contribute to optimizing the treatment approach for basketball players with Achilles tendinopathy, ultimately enhancing their pain management, functional recovery, and overall athletic performance.

AIM: This study aims to fill this gap by investigating the potential benefits of dry needling as a novel intervention for Achilles tendinopathy in basketball players. By examining its effects on pain reduction, functional improvement, tendon structure, and athletic performance, the research seeks to provide valuable insights into an effective and tailored treatment approach.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 40.00 Year(s)(—)
性别
All

入选标准

  • Confirmed Achilles Tendinopathy diagnosis of min 6 Week
  • Active competitive BasketBall Players.
  • Achilles Tendinopathy related functional impairment.
  • No Achilles Tendinopathy intervention done in past 3 months.

排除标准

  • History of Tendon Rupture.
  • History of Medical Condition.
  • History of Dry Needling In Achilles Tendinopathy.
  • Any Active Skin & Systemic Infection.
  • Any use of AntiCoagulants.
  • Physiological & Cognitive Disorders.

结局指标

主要结局

1. VAS,

时间窗: 1- Baseline | 2- 4 weeks | 3- 8 weeks

2. The Victorian Institute of

时间窗: 1- Baseline | 2- 4 weeks | 3- 8 weeks

Sport Assessment - Achilles

时间窗: 1- Baseline | 2- 4 weeks | 3- 8 weeks

(VISA-A) Questionnaire

时间窗: 1- Baseline | 2- 4 weeks | 3- 8 weeks

3. GONIOMETER

时间窗: 1- Baseline | 2- 4 weeks | 3- 8 weeks

4. FUNCTIONAL PERFORMANCE TEST

时间窗: 1- Baseline | 2- 4 weeks | 3- 8 weeks

次要结局

  • 1. PRESSURE ALGOMETER

研究者

发起方
NITISH KUMAR SRIVASTAVA
申办方类型
Other [INSTITUTE ]
责任方
Principal Investigator
主要研究者

NITISH KUMAR SRIVASTAVA

AMITY INSTITUTE OF HEALTH ALLIED SCIENCES

研究点 (1)

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