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临床试验/NCT05834153
NCT05834153已完成不适用

Comparative Effects of Kinesiotaping and Electrical Muscle Stimulation on Low Back Pain and Disability Associated With Diastasis Recti

Riphah International University2 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2022年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
48
试验地点
2
主要终点
Manual muscle testing MMT

研究概览

简要总结

To compare the effects of kinesiotaping and electrical muscle stimulation on low back pain and disability associated with diastasis recti.

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
20 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Diastasis recti more than 2 or 2.5cm
  • 6 weeks' postpartum cesarean section females
  • Primigravida females
  • Low back pain due to DR

排除标准

  • Normal vaginal delivery
  • Episiotomy
  • Multigravida women's
  • History of abdominal hernia
  • History of any abdominal surgery

研究组 & 干预措施

kinesiotaping

Experimental

干预措施: kinesiotaping (Device)

electrical muscle stimulation

Active Comparator

干预措施: electrical muscle stimulation (Device)

结局指标

主要结局

Manual muscle testing MMT

时间窗: 4th week

The strength of rectus abdominis muscle will recorded on a 0 to 5-point scale using manual muscle test suggested by Dr. Lovett. The patients will positioned in a supine, crook lying attitude with the arms straight by the side. The subjects will directed to lift and reach upwards till the scapular lower end level and if the subject will able to achieve and hold this position successfully then will ask to perform the next position by crossing the hands over the chest and then leaning forward and lifting the scapula off the table. After the patient achieved this position successfully forward reaching with hands crossed and supporting at the back of the head will perform. The scores will recorded based on the position that the patient could achieve and sustain successfully i.e. scores 3, 4 and 5 respectively for the above mentioned positions

Numeric pain rating scale

时间窗: 4th week

Numeric pain rating scale (an outcome measure) is a pain screening tool commonly used to assess pain severity using a 0 to 10 scale, with 0 measuring no pain and 10 meaning worst pain

Caliper method

时间窗: 4th week

Inter Recti Distance (IRD): The inter recti distance measurement was done by the use of a skin tone caliper. The IRD was measured at three levels both pre and post protocol, that is 2 or more than 2.5 cm above and below the umbilicus and at the umbilicus

Roland Morris Disability Questionnaire (RMDQ) for disability

时间窗: 4th week

The questionnaire was used to measure the level and severity of disability occurring due to low back pain reflected by higher numbers on a 24-point scale. The questionnaire was taken at the beginning and after completion of the protocol and the clinical improvement was calculated based on the score

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 (2)

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