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临床试验/NCT07086872
NCT07086872尚未招募不适用

Impact of Adding Integrated Neuromuscular Inhibition Technique to Mulligan Therapy in Symptomatic Forward Head Posture

Cairo University0 个研究点目标入组 120 人开始时间: 2025年7月30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
入组人数
120
主要终点
pain intensity

研究概览

简要总结

this study will be conducted to investigate the impact of adding integrated neuromuscular inhibition technique to mulligan therapy in symptomatic forward head posture.

详细描述

Forward head posture is anterior positioning of the cervical spine, which is regarded as a "bad" head posture and is commonly found in patients who experience problems with the head and neck. Particularly, forward head posture is frequently found in people sitting in front of a computer for prolonged periods. Load increases in the muscles and joints of the cervical spine as a result of forward head posture are considered a major cause of musculoskeletal disorders. INIT is effective as it causes sustained or intermittent compression which causes ischemia reduces local circulation until pressure is released, after which a flushing of fresh oxygenated blood occurs. Mechanoreceptors impulses interface with slower pain messages reducing amount of pain messges reaching the brain, releasing pain relieving hormones, decreasing myofascial pain. Stretches the taut bands of muscles fibers. INIT along with strengthening excercises proved to be beneficial in decreasing disability improving Range of motion. The concept of SNAG is to increase the treatment effects by having patients perform active movements while removing pain in the lesions by means of manipulative therapy. This is a new concept in the manipulative therapy field, and differs from traditional manipulative therapy by combining the active movements of the patients with additional passive movements performed with the aid of therapists

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)

盲法说明

opaque sealed envelope

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •CVA equal or less than 50
  • •Had cervical pain for more than three months and had visited an orthopedist clinic

排除标准

  • •cervical spine spondylosis
  • •fractures or cervical spinal surgery
  • •Cervical or shoulder neurological movement disorder.
  • •Temporo-mandibular surgery, (5) Pathologic trauma

研究组 & 干预措施

Integrated Neuromuscular Inhibition Technique and mulligan therapy

Experimental

thirty patients will receive Integrated Neuromuscular Inhibition Technique and mulligan therapy three times a weeks for six weeks+postural correction exercises

干预措施: Integrated Neuromuscular Inhibition Technique and mulligan therapy (Other)

Integrated Neuromuscular Inhibition Technique and mulligan therapy

Experimental

thirty patients will receive Integrated Neuromuscular Inhibition Technique and mulligan therapy three times a weeks for six weeks+postural correction exercises

干预措施: postural correction exercises (Other)

Integrated Neuromuscular Inhibition Technique

Experimental

thirty patients will receive Integrated Neuromuscular Inhibition Technique+postural correction exercises three times a weeks for six weeks

干预措施: Integrated Neuromuscular Inhibition Technique (Other)

Integrated Neuromuscular Inhibition Technique

Experimental

thirty patients will receive Integrated Neuromuscular Inhibition Technique+postural correction exercises three times a weeks for six weeks

干预措施: postural correction exercises (Other)

mulligan therapy

Experimental

thirty patients will receive mulligan Technique+postural correction exercises three times a weeks for six weeks

干预措施: mulligan therapy (Other)

mulligan therapy

Experimental

thirty patients will receive mulligan Technique+postural correction exercises three times a weeks for six weeks

干预措施: postural correction exercises (Other)

postural correction exercises

Active Comparator

thirty patients will receive postural correction exercises three times a weeks for six weeks

干预措施: postural correction exercises (Other)

结局指标

主要结局

pain intensity

时间窗: up to six weeks

visual analogue scale will be used to asses pain intensity which patient will be instructed to put point on line from no pain to tolerable pain. The scale consists of a line, usually 100 mm long, ranging from no pain or discomfort (zero) , to the worst pain that could possibly feel

次要结局

  • neck disability(up to 6 weeks)
  • pressure pain threshold(up to six weeks)
  • cervical range of motion(up to six weeks)
  • craniovertebral angle(up to six weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Al Shaymaa Shaaban Abd El Azeim

principle investigator : alshaymaa shaaban abd el azeim

Cairo University

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