Dry Dynamic Cupping vs Instrument-Assisted Soft Tissue Mobilization for Chronic Myofascial Low Back Pain
2026年6月29日 更新者：Ibadat International University, Islamabad
Comparative Effects of Dry Dynamic Cupping and Instrument-Assisted Soft Tissue Mobilization in Patients With Chronic Myofascial Low Back Pain
This study aims to compare the effects of Dry Dynamic Cupping and Instrument-Assisted Soft Tissue Mobilization (IASTM) in patients with chronic myofascial low back pain.
The interventions will be evaluated for their effectiveness in reducing pain, improving functional disability, and enhancing quality of life.
The findings may help identify a more effective treatment approach for managing chronic myofascial low back pain.
研究概览
地位
招聘中
研究类型
介入性
注册 (估计的)
48
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。
学习联系方式
- 姓名：MUHAMMAD ASHAR RAFI, DPT, MS-NMPT
- 电话号码：0092-308-3407837
- 邮箱：ashar.rafi@uipt.iiui.edu.pk
研究联系人备份
- 姓名：MUHAMMAD ARBAZ KHAN, DPT
- 电话号码：0092-333-9001698
- 邮箱：arbazkhantastic3@gmail.com
学习地点
-
-
Punjab Province
-
Rawalpindi、Punjab Province、巴基斯坦、46000
- 招聘中
- Mediplex Healthcare Center, Rawalpindi
-
-
参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
接受健康志愿者
不
描述
Inclusion Criteria:
- Chronic Myofascial Lower Back Pain > 3 months
- Pain reproduced by palpation of Lumbar Para-Spinals, Quadratus Lumborum (QL) or Thoracolumbar Fascia.
- Trigger Points will be diagnosed through Simons and Travell's Criteria
- Age 25-45 years (young adults according to WHO classification)
- Both genders
Exclusion Criteria:
- History of spinal surgery
- Presence of inflammatory or neurological disorders
- Facet joint dysfunction
- Discogenic pain
- Ligamentous pain
- Pregnant females
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
- 主要用途：治疗
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
有源比较器：Dry dynamic cupping group
Participants in this group will receive Dry Dynamic Cupping therapy.
The intervention will be administered for 2 weeks, with 3 treatment sessions per week, according to the standardized study protocol.
The effects of the intervention will be evaluated on pain intensity, functional disability, and lumbar range of motion.
|
Participants in this group will receive Instrument-Assisted Soft Tissue Mobilization (IASTM).
The intervention will be administered for 2 weeks, with 3 treatment sessions per week, according to the standardized study protocol.
The effects of the intervention will be evaluated on pain intensity, functional disability, and lumbar range of motion.
Participants in this group will receive Dry Dynamic Cupping therapy.
The intervention will be administered for 2 weeks, with 3 treatment sessions per week, according to the standardized study protocol.
The effects of the intervention will be evaluated on pain intensity, functional disability, and lumbar range of motion.
|
|
安慰剂比较：IASTM Group
Participants in this group will receive Instrument-Assisted Soft Tissue Mobilization (IASTM).
The intervention will be administered for 2 weeks, with 3 treatment sessions per week, according to the standardized study protocol.
The effects of the intervention will be evaluated on pain intensity, functional disability, and lumbar range of motion.
|
Participants in this group will receive Instrument-Assisted Soft Tissue Mobilization (IASTM).
The intervention will be administered for 2 weeks, with 3 treatment sessions per week, according to the standardized study protocol.
The effects of the intervention will be evaluated on pain intensity, functional disability, and lumbar range of motion.
Participants in this group will receive Dry Dynamic Cupping therapy.
The intervention will be administered for 2 weeks, with 3 treatment sessions per week, according to the standardized study protocol.
The effects of the intervention will be evaluated on pain intensity, functional disability, and lumbar range of motion.
|
研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
NPRS
大体时间：Baseline and 2 Weeks Post-Intervention
|
Pain intensity will be assessed using the Numeric Pain Rating Scale (NPRS), an 11-point scale ranging from 0 (no pain) to 10 (worst imaginable pain).
Changes in pain scores will be compared between the Dry Dynamic Cupping and IASTM groups.
|
Baseline and 2 Weeks Post-Intervention
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
ODI
大体时间：Baseline and 2 Weeks Post-Intervention
|
Functional disability related to low back pain will be assessed using the Oswestry Disability Index (ODI).
Changes in disability scores will be compared between groups.
|
Baseline and 2 Weeks Post-Intervention
|
其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Inclinometer
大体时间：Baseline and 2 Weeks Post-Intervention
|
Lumbar range of motion (ROM) will be measured using an inclinometer.
Flexion, extension, right and left side flexion, and right and left rotation will be assessed to evaluate changes in lumbar mobility following the intervention and compared between the Dry Dynamic Cupping and IASTM groups.
|
Baseline and 2 Weeks Post-Intervention
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员：MUHAMMAD ASHAR RAFI, DPT, MS-NMPT、Ibadat International University
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (实际的)
2026年1月1日
初级完成 (估计的)
2026年8月15日
研究完成 (估计的)
2026年9月1日
研究注册日期
首次提交
2026年6月29日
首先提交符合 QC 标准的
2026年6月29日
首次发布 (实际的)
2026年7月6日
研究记录更新
最后更新发布 (实际的)
2026年7月6日
上次提交的符合 QC 标准的更新
2026年6月29日
最后验证
2026年1月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.