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临床试验/NCT06387927
NCT06387927已完成不适用

The Effectiveness of Home-based Exercise Programs Versus Supervised Conventional Core Stability Exercises in Treatment of Chronic Mechanical, Non-specific Low Back Pain Patients With Controlled Hypertension

Ahram Canadian University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2023年9月2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
30
试验地点
1
主要终点
Assessment of pain

研究概览

简要总结

Thirty male and female hypertension patients with chronic mechanical non-specific low back pain were included in this randomized controlled study conducted at the Ababa Private Physical Therapy Center in Beni-Seuf, Egypt. They were randomly assigned into two equal groups; the study group A control (n = 15) had a supervised conventional core stability, while the study group B (n = 15) received a home exercise program. In both groups' patients had evaluations before and after their six-week course of therapy. Modified-modified Schober test was used to assess the active back range of motion (ROM), Arabic version of Oswestry disability index (ODI) was utilized to evaluate functional disability, and visual analog scale (VAS) was used to measure pain.

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, Care Provider)

入排标准

年龄范围
30 Years 至 50 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •hypertensive patient
  • •patient with chronic back pain
  • •The patients aged 30 to 50 years

排除标准

  • •Patients with vertebral fractures
  • •patient with surgical spinal fixation
  • •patient with rheumatic disorders
  • •patient with systemic diseases
  • •patient with multiple sclerosis.

研究组 & 干预措施

Group A (control) received supervised conventional core stability exercise program Study

Active Comparator

Group A (control) received supervised conventional core stability exercise program

干预措施: the core stability exercise (Other)

group B received a home-based exercise program

Experimental

Group B received a home-based exercise program.

干预措施: home exercise program (Other)

结局指标

主要结局

Assessment of pain

时间窗: up to 4 weeks

Pain was assessed using the visual analog scale

Assessment of functional disability

时间窗: up to 4 weeks

performed by Oswestry disability questionnaire version 2.0

Assessment of lumbar flexion range of motion

时间窗: up to 4 weeks

performed by modified modified schober test

次要结局

未报告次要终点

研究者

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

Mohamed Ababa

lecturer

Ahram Canadian University

研究点 (1)

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