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临床试验/CTRI/2025/07/090328
CTRI/2025/07/090328尚未招募1 期

Efficacy of Super Inductive System Therapy and Conventional Therapy in subjects with Upper Cross Syndrome - Randomized Controlled Trial

Dr Sanjana A Pammannavar1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2025年8月26日最近更新:

试验速览

阶段
1 期
状态
尚未招募
发起方
入组人数
66
试验地点
1
主要终点
1)Pain

研究概览

简要总结

This randomized controlled trial aims to evaluate the efficacy of Super Inductive System (SIS) therapy combined with conventional physiotherapy, compared to conventional therapy alone, in individuals diagnosed with Upper Cross Syndrome (UCS). UCS is a postural disorder characterized by muscle imbalances, including tightness in the upper trapezius and pectoral muscles and weakness in deep neck flexors and scapular stabilizers, leading to neck pain, postural deviations, and functional limitations.

A total of 66 participants aged 18–45 years with UCS will be randomly assigned to either the SIS + conventional therapy group or the conventional therapy-only group. Interventions will be conducted over four weeks, and outcomes will be assessed pre- and post-intervention using electromyography (EMG), pain pressure threshold, craniovertebral angle, postural assessment, kyphotic and shoulder angles, functional mobility (NDI), and cervical ROM.

The study aims to provide objective evidence on the effectiveness of SIS in improving muscle activation, posture, and reducing pain in UCS patients.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 45.00 Year(s)(—)
性别
All

入选标准

  • Adults aged 18–45 years diagnosed with Upper Cross Syndrome based on clinical assessment.
  • Complaints of neck pain for at least three months.
  • Pain Pressure Threshold more or equal 2.5 N per cm2 over UCS-affected muscles.
  • Craniovertebral angle more or equal48 degrees indicating forward head posture.
  • Neck Disability Index score less or equal 10 percent, indicating functional limitations.
  • Willingness to participate in the study.

排除标准

  • History and recent diagnosis of cervical spine pathology such as herniated disc, cervical spondylosis, or spinal fractures.
  • Neurological disorders affecting muscle function.
  • Recent trauma, surgery, or injury to the neck, shoulder, or upper back within the last six months.
  • Severe musculoskeletal conditions such as rheumatoid arthritis, ankylosing spondylitis.
  • Pregnant or lactating women.
  • Implants or Pacemaker in the Upper quadrant of the body.
  • Skin infections, open wounds, or dermatological conditions in the treatment area.
  • Uncontrolled metabolic disorders.
  • Presently on any other Alternative therapy.

结局指标

主要结局

1)Pain

时间窗: Day of intervention and post intervention 4th week

2)ROM

时间窗: Day of intervention and post intervention 4th week

3)Craniovertebral angle

时间窗: Day of intervention and post intervention 4th week

4)Strength.

时间窗: Day of intervention and post intervention 4th week

次要结局

  • 1)Posture(2)Kyphotic angle)

研究者

发起方
Dr Sanjana A Pammannavar
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Sanjana A Pammannavar

K.L.E Institute of Physiotherapy

研究点 (1)

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