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临床试验/NCT07292051
NCT07292051尚未招募不适用

Effect of Blood Flow Restriction Technique on Postpartum Pelvic Girdle Pain

Kafrelsheikh University0 个研究点目标入组 66 人开始时间: 2025年12月12日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
66
主要终点
pelvic girdle pain intensity ( pain index )

研究概览

简要总结

Purpose of the study :

The purpose of the current study is investigating the effect of Blood Flow Restriction Training technique on postpartum pelvic girdle pain.

详细描述

This study is a randomized controlled trial. To fulfill its purpose, we have two groups; control group (A) and experimental group (B) are two matched postpartum pelvic girdle pain groups. While group (A) will receive a core stability exercise program, group (B) will receive core stability exercise program with blood flow restriction technique.

The primary outcome measure will be pelvic girdle pain intensity, while the secondary outcomes will include pelvic girdle-related disability, health-related quality of life, Kinesiophobia , global improvement and ASLR-RE angle.

Treatment duration will be eight weeks.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 35 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Patients will be eligible for the study if they met all the following criteria:
  • Are between 3 and 12 months postpartum.
  • Are aged between 20 and 35 years.
  • Have a body mass index (BMI) < 30 kg/m².
  • Reported experiencing pelvic girdle pain-defined as pain localized between the posterior iliac crest and the gluteal fold, particularly in the vicinity of the sacroiliac joints-that either began during pregnancy or persisted after delivery .
  • Presented with a positive Active Straight Leg Raise (ASLR) test.
  • Showed positive findings in at least two of the following six pelvic pain provocation tests:
  • Posterior Pelvic Pain Provocation (P4/Thigh Thrust) Test
  • Patrick's (FABER) Test
  • Long Dorsal Sacral Ligament Test
  • Pelvic Compression Test
  • Pelvic Distraction (Separation) Test
  • Sacral Thrust Test

排除标准

  • -Patients will be excluded if they have any of the following:
  • If they were Pregnant
  • Known causes of pelvic girdle pain, such as fractures and rheumatism
  • Undergone lumbar or pelvic surgery in the past
  • Current neurological symptoms and signs in lower extremities such as lumbar radiculopathy and myelopathy
  • Cardiovascular disease
  • Experience with structured and supervised core or trunk exercise training programs

结局指标

主要结局

pelvic girdle pain intensity ( pain index )

时间窗: Baseline , 8 weeks and 16 weeks

In this study, pain severity will be measured using the mean of three 11-point NRS questionnaires for least, usual, and current pain over the previous 2 weeks.

次要结局

  • pelvic girdle-related disability(Baseline , 8 weeks and 16 weeks)
  • Health-related quality of life(Baseline , 8 weeks and 16 weeks)
  • Kinesiophobia(Baseline , 8 weeks and 16 weeks)
  • Global improvement(Baseline , 8 weeks and 16 weeks)
  • Active straight leg raises repositioning error (ASLR-RE)(Baseline , 8 weeks and 16 weeks)

研究者

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

Nour Abdelaty Attia El-desouky

Physical Therapist

Kafrelsheikh University

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