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临床试验/NCT07710235
NCT07710235已完成不适用

Comparative Effects of Dry Needling and Kinesio Taping as Adjuncts to Strength Training on Pain, Functional Mobility, and Quality of Life in Patients With Knee Osteoarthritis: A Three-Arm Randomized Controlled Trial

Foundation of Medical Research and Laboratories, Pakistan1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2024年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
50
试验地点
1
主要终点
Numeric Pain Rating Scale (NPRS)

研究概览

简要总结

To compare the effects of dry needling and Kinesio taping, each combined with strength training, on pain, functional mobility, and quality of life in patients with knee OA.

详细描述

Background: Knee osteoarthritis (OA) is a progressive degenerative joint condition characterized by pain, myofascial trigger points, muscular weakness, and impaired functional mobility, ultimately affecting quality of life. Strength training is widely recommended as a first-line conservative treatment; however, residual pain and myofascial dysfunction may limit optimal recovery. Dry needling has been shown to deactivate trigger points and reduce local muscle hypertonicity, while Kinesio taping is proposed to modulate pain and support proprioception and muscle function through cutaneous and fascial mechanisms. Comparative evidence on the added benefit of these two adjunct techniques alongside strength training in knee OA remains scarce.

Objective

To compare the effects of dry needling and Kinesio taping, each combined with strength training, on pain, functional mobility, and quality of life in patients with knee OA.

Methodology: A three-arm parallel-group randomized controlled trial was conducted on 50 participants diagnosed with knee OA (Kellgren-Lawrence grade II-III), randomly allocated into three groups using a computer-generated random sequence with allocation concealment. Group A received dry needling combined with strength training, Group B received Kinesio taping combined with strength training, and Group C received strength training alone as the control group. Interventions were administered three times per week for 6 weeks. Outcome measures included the Numeric Pain Rating Scale (NPRS) for pain, the Timed Up and Go (TUG) test for functional mobility, and the WHOQOL-BREF for quality of life, assessed at baseline and post-intervention (6 weeks). Data were analyzed using repeated-measures ANOVA and post-hoc comparisons, with significance set at p<0.05.

研究设计

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

入排标准

年龄范围
45 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient with knee osteoarthritis, Age between 45-65 years, VAS 7 or above.

排除标准

  • Known allergic conditions, refused to give written consent to participate in the study not fallen in inclusion criteria.

结局指标

主要结局

Numeric Pain Rating Scale (NPRS)

时间窗: 6 weeks

The value were taken at base line and after 6 weeks of intervention

Timed Up and Go (TUG)

时间窗: 6 weeks

The value were taken at base line and after 6 weeks of intervention

WHOQOL-BREF

时间窗: 6 weeks

The value were taken at base line and after 6 weeks of intervention

次要结局

未报告次要终点

研究者

发起方
Foundation of Medical Research and Laboratories, Pakistan
申办方类型
Other
责任方
Sponsor

研究点 (1)

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