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临床试验/CTRI/2025/07/091762
CTRI/2025/07/091762尚未招募不适用

Effectiveness of KIASTM and Motor Control Training Exercises in patients with chronic nonspecific neck pain

Lopa Das1 个研究点 分布在 1 个国家目标入组 69 人开始时间: 2025年8月5日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
69
试验地点
1
主要终点
Outcome measures includes:

研究概览

简要总结

The proposed study shall conclude a detailed analysis of finding an innovative treatment protocol for subjects suffering from chronic nonspecific neck pain.

Use of advanced tools like Kinesio Instrument Assisted Soft Tissue Mobilization (KIASTM) and its effectiveness in treating nonspecific neck pain shall give more scope for managing other musculoskeletal conditions.

Addition of KIASTM tool for treating myofascial pain syndrome which is depicted as primary symptoms of nonspecific neck pain cases along with Motor Control Training Exercises will give a deeper insight into the literature concerning IASTM and also strengthening of deep neck muscles.

Application of Motor Control Training Exercises will address the motor control dysfunction issues which is profoundly associated among chronic nonspecific neck pain patients.

研究设计

研究类型
Interventional
分配方式
Na
盲法
Investigator 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

  • Subjects clinically diagnosed with chronic non specific neck pain with symptoms more than 3 months by physician Subjects with negative spurling’s test Age Group : 18-40 Both male and female subjects Subjects who are willing to participate in the study.

排除标准

  • Subjects with history of recent spinal surgery, spinal fractures ,any carcinogenic conditions , Subjects diagnosed with Cervical radiculopathy ,cervical myelopathy, Cervicogenic headache.

结局指标

主要结局

Outcome measures includes:

时间窗: At baseline,3 weeks

Visaul analogue scale

时间窗: At baseline,3 weeks

Range of Motion goniometry

时间窗: At baseline,3 weeks

Neck Disability Index

时间窗: At baseline,3 weeks

Deep Neck Flexor Testing

时间窗: At baseline,3 weeks

SF-36 score

时间窗: At baseline,3 weeks

Serum Biomarker level

时间窗: At baseline,3 weeks

次要结局

未报告次要终点

研究者

发起方
Lopa Das
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Lopa Das

Garden City University

研究点 (1)

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