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临床试验/NCT07484360
NCT07484360已完成不适用

Effects of Kinetic Chain Exercises on Pain, Range of Motion and Disability in Shoulder Impingement Syndrome

Riphah International University1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2025年7月10日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
36
试验地点
1
主要终点
Numeric Pain Rating scale

研究概览

简要总结

PROJECT SUMMARY Shoulder pain is secondary only to lower back pain in occurrence. Impingement is one of the most common shoulder disorders. The aim of this study is to evaluate the effects of kinetic chain exercises on pain, ROM and disability in patients with shoulder impingement syndrome which is important in establishing eveidence for a holistic and potentially more effective rehabilitation method for shoulder impingement syndrome. This study will be a randomized control trial and will be conducted in Riphah International University associated hospital and physiotherapy outpatient department of Jinnah hospital Lahore.

Non probability consecutive sampling will be used. Sample size of 32 subjects with age group 30 to 50 years will be taken. Data will be collected from patients having present complaint of shoulder pain due to shoulder impingement. Outcome measures will be taken using numeric pain rating scale(NPRS) for pain, universal Goniometer for ROM and Shoulder pain and disability index (SPADI) for function. An informed consent will be taken. Subjects will be selected on the basis of inclusion and exclusion criteria and will be equally divided into two groups. Group A will receive kinetic chain exercises (both open and closed chain exercises) and group B will receive conventional physical therapy treatment. Data analysis will be done by SPSS version 28

详细描述

PROJECT SUMMARY Shoulder pain is secondary only to lower back pain in occurrence. Impingement is one of the most common shoulder disorders. The aim of this study is to evaluate the effects of kinetic chain exercises on pain, ROM and disability in patients with shoulder impingement syndrome which is important in establishing eveidence for a holistic and potentially more effective rehabilitation method for shoulder impingement syndrome. This study will be a randomized control trial and will be conducted in Riphah International University associated hospital and physiotherapy outpatient department of Jinnah hospital Lahore.

Non probability consecutive sampling will be used. Sample size of 32 subjects with age group 30 to 50 years will be taken. Data will be collected from patients having present complaint of shoulder pain due to shoulder impingement. Outcome measures will be taken using numeric pain rating scale(NPRS) for pain, universal Goniometer for ROM and Shoulder pain and disability index (SPADI) for function. An informed consent will be taken. Subjects will be selected on the basis of inclusion and exclusion criteria and will be equally divided into two groups. Group A will receive kinetic chain exercises (both open and closed chain exercises) and group B will receive conventional physical therapy treatment. Data analysis will be done by SPSS version 28

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
30 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • • Age group 30-50 years
  • Males and Females
  • Subjects with history of pain in upper lateral aspect of arm with a NPRS score between >3 to <8 on a 0-10 scale
  • Neers impingement test positive
  • Hawkins- Kennedy test positive
  • Painful arc positive
  • Empty can (Jobe test) positive

排除标准

  • • Subjects having Capsular Pattern +ve
  • Individuals with OA of GH joint
  • Type III acromion process decreasing the sub-acromial space leading to sub-acromial impingement (on X-ray evaluation)
  • AC joint arthritis
  • Rheumatoid Arthritis
  • Fracture history involving upper limb
  • Shoulder surgery on affected side.
  • Subjects with signs of total rotator cuff tears i.e. gross weakness in abduction.
  • Subjects who received corticosteroid injections in last three months

结局指标

主要结局

Numeric Pain Rating scale

时间窗: from start of study to 4 weeks

. This scale ranges from 0 to 10 where 0 indicating "no pain" and 10 indicating "worst pain possible"

Shoulder Pain and Disability Index

时间窗: From start of study upto 4 weeks

The Shoulder Pain and Disability Index (SPADI) is a self-administered questionnaire that consisting of two dimensions, one for the pain and other for functional ability of the subject. The pain dimension consists of five questions regarding the severity of an individual's pain intensity

Universal Goniometer

时间窗: From start of study upto 4 weeks

Health care practitioners often use universal goniometer to obtain objective measurements of joint range of motion (ROM) to find out the baseline functional status and to measure the effectiveness of treatment interventions

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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