跳至主要内容
临床试验/NCT07702617
NCT07702617尚未招募不适用

Effects Of Vacuum Controlled Static Versus Vacuum Controlled Dynamic Dry Cupping On Pain, Range Of Motion And Disability Among Patients With Chronic Low Back Pain

Lahore University of Biological and Applied Sciences1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2026年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
48
试验地点
1
主要终点
Pain Intensity

研究概览

简要总结

This randomized controlled clinical trial aims to compare the effects of vacuum-controlled static dry cupping and vacuum-controlled dynamic dry cupping on pain intensity, lumbar range of motion, and functional disability in patients with chronic low back pain. Participants will be randomly assigned to two groups receiving either static or dynamic dry cupping along with conventional treatment. The outcomes will be assessed to determine which cupping technique is more effective in improving pain, mobility, and functional ability in individuals with chronic low back pain.

[Time Frame: Measured at baseline (pre-intervention) and after 6 weeks (post-intervention completion).

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
30 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age 30 to 40 years. (21)
  • Both male and female genders (15)
  • Patients experiencing LBP with a score of at least 3/10 on the NPRS (22)
  • For more than three months (22).
  • Individuals whose workstations have not been ergonomically designed and who have not previously received structured ergonomic interventions related to workplace layout, task design, or load modification also involving home tasks and daily activities. (31)

排除标准

  • * Subjects with lower body condition (i.e., spondylolisthesis, spinal stenosis, osteoporosis, or intervertebral disk derangement) (15)
  • Subjects with a history of cancer (15)
  • Subjects experiencing referred leg symptoms (15)
  • Subjects with any current local or systemic infections, vascular disease, including varicose veins (17)
  • History of spine surgery or spinal tumor (17).

研究组 & 干预措施

Static Dry Cupping

Experimental

Participants in this group will receive vacuum-controlled static dry cupping applied to the lumbar region. The cups will be placed on specific points over the lower back and kept stationary for approximately 10 minutes per session along with conventional physiotherapy management for chronic low back pain.

干预措施: Vacuum-Controlled Static Dry Cupping (Other)

Dynamic Dry Cupping

Active Comparator

Participants in this group will receive vacuum-controlled dynamic dry cupping applied to the lumbar region. After creating negative pressure, the cups will be gently moved over the lower back to mobilize soft tissues along with conventional physiotherapy management for chronic low back pain.

干预措施: Vacuum-Controlled Dynamic Dry Cupping (Other)

结局指标

主要结局

Pain Intensity

时间窗: Baseline (before treatment) and after 6 weeks of intervention.

Pain intensity in patients with chronic low back pain will be assessed using the Numeric Pain Rating Scale (NPRS). The NPRS is an 11-point scale ranging from 0 to 10, where 0 indicates no pain and 10 represents the worst imaginable pain. It will be used to evaluate the effectiveness of vacuum-controlled static and dynamic dry cupping in reducing pain levels.

Lumbar Range of Motion

时间窗: Baseline (before treatment) and after 6 weeks of intervention.

Lumbar range of motion will be measured to assess improvement in spinal mobility in patients with chronic low back pain. Lumbar movements including flexion, extension, and lateral flexion will be evaluated using a goniometer or inclinometer.

Functional Disability

时间窗: Baseline (before treatment) and after 6 weeks of intervention.

Functional disability related to chronic low back pain will be assessed using the Oswestry Disability Index (ODI), a validated questionnaire that measures the impact of back pain on daily activities such as walking, sitting, standing, and personal care.

次要结局

未报告次要终点

研究者

发起方
Lahore University of Biological and Applied Sciences
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验