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临床试验/NCT06705933
NCT06705933已完成不适用

Effect of Kinesiotaping on Postpartum Pelvic Girdle Pain

Cairo University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年11月27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
60
试验地点
1
主要终点
Assessment of pain

研究概览

简要总结

The purpose of this study is to investigate the effect of kinesiotaping on pelvic girdle pain in postpartum women.

详细描述

Pregnancy-related pain in the SIJ, lumbosacral region, pubic symphysis, or in any combination of these joints has been coined as pelvic girdle pain (PGP) and has been estimated to affect almost half of all pregnant women. Women with PGP have an increased risk of prenatal anxiety, depressive symptoms and postpartum depression compared with healthy pregnant women.

Kinesio Taping is rehabilitative technique used to facilitate the body's natural healing process while providing support and stability to muscles and joints, without restricting their range of motion. Enhanced rehabilitation is thought to be the effect of stimulated reactivation, proprioceptive training, reduced pain, stimulation of correct movement patterns, and reduction of muscle imbalance.

Kinesio Taping (KT) method has been used to decrease and prevent pain in women suffering from pregnancy related low back pain because of increased muscle relaxation while taping is applied. However, there is lack of knowledge regarding the effect of kinesiotaping on PGP in postpartum women.

Therefore, this study will be conducted to provide physiotherapists with a scientific updated knowledge, concerning the effect of kinesiotaping on pain, level of disability and lumbar flexion and extension ROM in pelvic girdle pain in postpartum women, aiming to improve ADLs of postpartum women. This study may expand the role of physiotherapy in women's health

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
25 Years 至 35 Years(Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •All post-partum women < 4 months postnatal having pelvic girdle pain.
  • •They will be diagnosed using Faber test, and active straight leg raising test.
  • •Their ages will range from 25 to 35 years.
  • •Their body mass index (BMI) less than 30 kg/ m².

排除标准

  • •Pregnant women or planning for pregnancy.
  • •Cardiovascular diseases.
  • •Previous spinal surgery.
  • •History of skeletal deformity.
  • •Participation at any other exercise training program during this study

研究组 & 干预措施

Core stability exercise and myofascial release group

Active Comparator

The participants will receive core stability exercise and myofascial release for 20 min three times per week for 8 weeks.

干预措施: Core stability exercise (Other)

Core stability exercise and myofascial release group

Active Comparator

The participants will receive core stability exercise and myofascial release for 20 min three times per week for 8 weeks.

干预措施: Myofascial release (Other)

Kinesiotaping, in addition to core stability exercise and myofascial release group

Experimental

The participants will receive kinesiotaping, in addition to core stability exercise and myofascial release for 8 weeks

干预措施: Core stability exercise (Other)

Kinesiotaping, in addition to core stability exercise and myofascial release group

Experimental

The participants will receive kinesiotaping, in addition to core stability exercise and myofascial release for 8 weeks

干预措施: Myofascial release (Other)

Kinesiotaping, in addition to core stability exercise and myofascial release group

Experimental

The participants will receive kinesiotaping, in addition to core stability exercise and myofascial release for 8 weeks

干预措施: Kinesiotaping (Other)

结局指标

主要结局

Assessment of pain

时间窗: 8 weeks

Visual analog scale will be used to assess pain level in each woman in both groups before and after the treatment program. The score is determined by measuring the distance (mm) on the 10-cm line between the "no pain" anchor and the patient's mark, providing a range of scores from 0-100. A higher score indicates greater pain intensity. The following cut points on the pain VAS have been recommended: no pain (0-4 mm), mild pain (5-44 mm), moderate pain (45-74 mm), and severe pain (75-100 mm)

次要结局

  • Measurement of disability level(8 weeks)
  • Assessment of lumbar flexion range of motion (ROM)(8 weeks)
  • Assessment of lumbar extension range of motion (ROM)(8 weeks)

研究者

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

Mariam Sobhy Kamal mohareb

Principal investigator

Cairo University

研究点 (1)

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