跳至主要内容
临床试验/NCT05015413
NCT05015413Unknown不适用

Effect of Shockwave Versus Low Level Laser Therapy on Sacroiliac Joint Pain in Postnatal Women

Samar Mimi Mohamed Okby0 个研究点目标入组 50 人开始时间: 2021年11月25日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
50
主要终点
Sacroiliac joint pain

研究概览

简要总结

Sacroiliac joint pain is the most causes of back pain In pregnancy caused ligament laxity in sacroiliac joint so cause pain and this pain continue after natal Shock wave is new conservative treatment used in physical therapy Shock wave is most effective for sacroiliac joint pain Low level laser is a most effective pain relive and effective on sacroiliac joint pain

详细描述

The study is to determine if there is any difference between the effect of shockwave and low level laser therapy on sacroiliac joint pain in postnatal women This study will be randomly distributed into two equal group Group A consisted of 25 postpartum women complaining from sacroiliac joint pain . They will receive shockwave therapy 2 session per week for 6 weeks Group B consisted of 25 postpartum women complaining from sacroiliac joint pain . They will receive low level laser therapy 2 session per week for 6 weeks

Evaluation procedures History taking recording in recording data sheet Weight and height measurement by calculate BMI Disability assessment by OWDI Pain assessment by VAS scale Assessment of pressure of pain threshold by pressure algometry

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
None

入排标准

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

入选标准

  • postnatal women suffering from sacroiliac joint pain for at least 3 months.
  • They should have moderate to severe pain .
  • They should have positive findings in at least 3 of 5 provocation sacroiliac joint tests

排除标准

  • lumber or hip joint pathology
  • Acute pelvic bacterial or viral infection .
  • Receiving corticosteroid injections within the previous 6 weeks

结局指标

主要结局

Sacroiliac joint pain

时间窗: About two months

•Pain intensity: it will by measure by VAS it's presented as 10 cm horizontal line on which the patient pain intensity is point between no pain at zero score to extreme pain at 10 score .

Functional disability

时间窗: About 2 month

•Functional disability :it will be measure by oswestry disability index it is 10 point Patient reported outcome questionnaire which the higher score mean its the worst and the low score mean its the better outcome.

Pain pressure threshold

时间窗: About 2 month

•Pain pressure threshold : it will be measure by a device Called pressure algometry

次要结局

未报告次要终点

研究者

发起方
Samar Mimi Mohamed Okby
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Samar Mimi Mohamed Okby

Physical therapist in al Agoza police hospital

Cairo University

相似试验

Effect of Shockwave Versus LLL Therapy on Sacroiliac... | 临床试验