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临床试验/NCT07418346
NCT07418346已完成不适用

Evaluating Pain and Functional Outcomes of Active Release Technique Versus Strain-counter- Stain in Chronic Low Back Pain .A Randomized Clinical Trial

Ibadat International University, Islamabad1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年5月5日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
Visual analogue scale (VAS)

研究概览

简要总结

clinical trial aims to compare the effects of Active Release Technique (ART) and Strain-Counter-Strain (SCS) on pain reduction and functional improvement in male patients aged 30-45 years with chronic low back pain (CLBP) persisting for at least 3-4 months. CLBP is a widespread and debilitating condition with significant impact on quality of life, healthcare costs, and work productivity. ART focuses on releasing myofascial adhesions and alleviating trigger points through manual pressure and movement, while SCS is a passive positional technique designed to reduce neuromuscular tension and restore range of motion.

A total of 40 participants will be randomly allocated into two equal groups (ART group and SCS group). Both groups will receive standardized baseline treatment including a hot pack and interferential current therapy, followed by their respective intervention protocols for 12 sessions over 4 weeks. Pain intensity will be measured using the Visual Analogue Scale (VAS), functional disability using the Quebec Back Pain Disability Scale (QBPDS), and functional limitation using the Oswestry Disability Index (ODI). Data will be analyzed using SPSS v25, applying paired and independent t-tests or their non-parametric equivalents, with a significance level of p < 0.05.

The study is expected to provide evidence-based insight into which intervention is more effective in improving pain and functional outcomes in CLBP. The findings may help guide clinical decision-making, contribute to treatment guidelines, and support cost-effective, patient-centered management approaches.

详细描述

Chronic low back pain (CLBP) is a globally prevalent and debilitating condition that significantly impacts patients' functional capacity, quality of life, work productivity, and healthcare systems. Its multifactorial etiology, varied patient presentations, and inconsistent responses to treatment make CLBP a persistent therapeutic challenge. Non-pharmacological approaches such as Active Release Technique (ART) and Strain-Counter-Strain (SCS) have emerged as promising interventions, yet there is limited and inconsistent high-quality evidence comparing their effectiveness in CLBP management.

ART is a soft tissue manual therapy targeting myofascial adhesions, scar tissue, and trigger points. By applying specific manual pressure combined with patient movement, ART aims to restore normal muscle texture, reduce tension, and improve function. It is commonly used for pain associated with muscle tightness, restricted mobility, and neuromuscular dysfunction.

SCS is a passive positional release technique that reduces muscle spasm and tension by placing the affected muscle in a shortened position for a set duration, typically 90 seconds, followed by a gradual return to neutral. It works by reducing proprioceptive activity in muscle spindles, thereby alleviating pain and restoring motion.

This randomized clinical trial will recruit 40 male participants aged 30-45 years diagnosed with CLBP persisting for at least 3-4 months, with pain intensity ≥4/10 on the Visual Analogue Scale (VAS). Patients will be randomly allocated into two equal groups-Group A: ART and Group B: SCS-using a sealed card draw method. Both groups will receive a standardized pre-treatment protocol consisting of a 10-minute hot pack application to the lower back and 15 minutes of interferential current therapy.

Intervention Protocol:

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
30 Years 至 45 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Patient will be diagnosed by the therapist.
  • Individuals diagnosed with chronic low back pain persisting for at least 3-4 months.
  • Patients aged 30-45 years.
  • Only men will be included in this study
  • Pain intensity of at least 4/10 on the Visual Analogue Scale (VAS)

排除标准

  • Patients with a history of spinal surgery or significant spinal conditions (e.g., fractures, tumors, infections).
  • Individuals with neurological disorders like cauda equine, radiculopathy and spinal stenosis affecting the lower back or lower extremities.
  • Pregnant women or individuals with contraindications to ART or strain-counter-strain therapy.
  • Patients unable to provide informed consent or adhere to treatment protocols.

结局指标

主要结局

Visual analogue scale (VAS)

时间窗: fram enlloment to the end of treatment it 4 week

pain intensity

Oswerty disability index ODI

时间窗: fram enlloment to the end of treatment it 4 week

functional limitation

Quebec back pain disability (QBPDS)

时间窗: fram enlloment to the end of treatment it 4 week

functional disability

次要结局

未报告次要终点

研究者

发起方
Ibadat International University, Islamabad
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Mudassar Ali

assistant professor

Ibadat International University, Islamabad

研究点 (1)

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