跳至主要内容
临床试验/NCT06814704
NCT06814704已完成不适用

Effect of Intraabdominal Hypopressive Exercises on Postnatal Backache and Functional Disability

Kafrelsheikh University1 个研究点 分布在 1 个国家目标入组 38 人开始时间: 2024年3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
38
试验地点
1
主要终点
Pain assessment

研究概览

简要总结

The purpose of this study was to evaluate the effectiveness of hypopressive exercise in postpartum females with abnormal hyperlordosis and back pain.

Hypopressive exercises are safe and beneficial for new moms, as they can be started soon after delivery. They help strengthen postural muscles, reduce back pain, and manage pain by reducing intra-abdominal pressure, increasing activity of postural musculature, and normalizing myofascial tension.

详细描述

38 postpartum women with abnormal hyperlordosis. The women were then divided into two equal groups. Group A(n=19) received hypopressive abdominal exercise along with traditional treatment for lower back pain (LBP), while Group B(n=19) received the same treatment without hypopressive exercise. The main outcomes measured were the the Revised Short McGill Pain Questionnaire Version-2, the lumbar lordotic angle, and the patient-specific functional scale.

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 (Participant)

入排标准

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

入选标准

  • •participants must have a healthy pregnancy, a typical vaginal birth, LBP that existed 24 weeks after giving birth, and functional limitations in daily activities. The study only allowed women aged 20-35 with no more than two prior pregnancies and a BMI of less than 25 kg/m2 to participate.

排除标准

  • •women who under pharmacological or psychological treatment, had pelvic tumors, lumbar disk herniation, heart disease, hypertension, lumbar spine tumors, chronic uterine prolapse, chronic pelvic pain, lumbar spondylosis, or lumbar spondylolisthesis.

研究组 & 干预措施

Group (A)

Experimental

Group A will receive 1. hypopressive abdominal exercises 2. traditional treatment for low back pain (Pharmacological treatment (paracetamol 0.5-1g 3times/day),Heat therapy Continuous low-level heat wrap(electrical) 3. Progressive strength training.

干预措施: Hypopressive exercises , hot packs, acetaminophen, progressive strengthening exercises (Other)

Group (B)

Placebo Comparator

Group B will receive 1. traditional treatment for low back pain (Pharmacological treatment (paracetamol 0.5-1g 3times/day),Heat therapy Continuous low-level heat wrap(electrical) 2. Progressive strength training.

干预措施: heat therapy, pharmacological therapy, progressive strengthening exercises (Other)

结局指标

主要结局

Pain assessment

时间窗: Pain assessment at the end of the study up to 8 weeks

pain: The Revised Short McGill Pain Questionnaire will be used to assess both groups before and after the study.

次要结局

  • Assessment of functional disability(This scale will be done for each case at the end of the study up to 8 weeks)

研究者

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

Salwa A. Shawat

Principle Investigator

Kafrelsheikh University

研究点 (1)

Loading locations...

相似试验