跳至主要内容
临床试验/NCT07724600
NCT07724600尚未招募不适用

Effects of Active Release Technique Versus Stecco Facial Manipulation on Pain, Craniovertebral Angle, and Functional Disability in Patients With Chronic Non-specific Neck Pain.

Riphah International University0 个研究点目标入组 48 人开始时间: 2026年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
48
主要终点
Numeric pain rate scale

研究概览

简要总结

Non-specific pain that originates from the superior nuchal line and extends to the first thoracic vertebrae. It is exacerbated by sustained neck postures, neck movements or cervical muscle palpation. Neck pain is a work-related musculoskeletal disease that can arise during prolonged or high-intensity activity. Increasingly, individuals seek medical attention for discomfort in the neck, upper extremities, and head caused by chronic tension. Neck discomfort is often caused by mechanical dysfunction that restricts joint movement inside the joint capsule. Active Release Technique(ART) is a manual release of tight soft tissue which targets on SCM, levator scapulae, suboccipital and Upper trapezius. Stecco Fascial Manipulation is an efficient manual soft tissue treatment method that particularly address in the areas of myofascial pain and discomfort, locomotor issues, and posture dysfunction. The aim of this study is to treat the patients having chronic non specific neck pain through the Active Release Technique (ART) and Stecco Facial Manipulation and to compare their effects that can affect cervical flexibility and to improve the symptom parameters of the regarding individual.

详细描述

The current study will be Randomized Clinical Trial. Inclusion criteria for this study is the individual with chronic non specific neck pain between the age group of 20-40yr. Patient with any history of trauma or surgery in cervical region and any other cervical pathology will be excluded from the study. A sample of 44 individual with CNSNP will be selected from both genders. Tools used for the Data collection will be Numeric Pain Rating Scale(NPRS), Neck Disability Index(NDI) and Goniometer. Participants will be measured before and after treatment to assess changes. Interventions are carried out 5 days in a week for one hour daily. In this study descriptive statistical tools will used to analyze the data. Data will be analyzed through SPSS version 21.

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 (Outcomes Assessor)

入排标准

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

入选标准

  • Individuals of both genders
  • Age between 20-40yrs(19).
  • Neck pain persisting for more than 3 months
  • Neck Disability Index (NDI) score between 10-30) (20).

排除标准

  • Patients with history of trauma or surgery were excluded.
  • Cervical pain patients with radiculopathy were excluded.
  • Patients diagnosed cases of rheumatoid arthritis, or any systemic musculoskeletal disorders were excluded.
  • Patients use of muscle relaxants or undergoing any other physiotherapy for neck issues in the past 3 months were excluded.
  • Patients with cervical disc herniation or whiplash injuries were excluded.
  • Pregnancy or known hormonal conditions affecting musculoskeletal system were excluded.

结局指标

主要结局

Numeric pain rate scale

时间窗: upto 6 weeks

The numerical rating scale (0-10), with 0 meaning no pain, and 10 meaning the worst unbearable pain, as measurement of pain intensity.

次要结局

  • 2. Universal Goniometer(upto 6 weeks)
  • Neck Disability index for functional Disability (NDI)(upto 6 weeks)
  • Flexion Rotation Test(upto 6 weeks)

研究者

申办方类型
Other
责任方
Sponsor

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