跳至主要内容
临床试验/CTRI/2025/07/090718
CTRI/2025/07/090718Not Applicable不适用

Efficacy of Core Strengthening Exercise versus Pilates Exercise for Mechanical Low Back Pain

Department of Physiotherapy and Rehabilitation2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年7月26日最近更新:

试验速览

阶段
不适用
状态
Not Applicable
发起方
入组人数
50
试验地点
2
主要终点
Core Strength: Pressure Biofeedback

研究概览

简要总结

This study aims to compare the effects of core strengthening exercises and Pilates exercises on individuals with mechanical low back pain. Participants aged between 20 and 60 years, experiencing non-specific low back pain for at least 3 months and reporting a pain level of 3 or higher on the Visual Analogue Scale (VAS), will be included. The study will be conducted as a randomized clinical trial at the Department of Physiotherapy and Rehabilitation, Jashore University of Science and Technology. Participants will be randomly assigned to either a core strengthening group or a Pilates exercise group. The interventions will be delivered by qualified physiotherapists. The primary outcome measure will be core strength assessed by pressure biofeedback. Secondary outcomes include pain, functional disability, and quality of life measured using validated tools. The study follows the CONSORT reporting guideline and is partially funded by the Department of Physiotherapy and Rehabilitation at JUST

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant Blinded

入排标准

年龄范围
20.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • 01.NSLBP for at least 3 months 02.Experienced a pain intensity of 3 or higher based on the visual analogue scale (VAS, 0-10)
  • All male and female adults between age group of 20–60 years
  • Subjects willing to participate in the study.

排除标准

  • 01.History of spinal surgery 02.History of ankylosing spondylitis or rheumatoid arthritis 03.History of spondylolisthesis or spondylolysis 04.History of spinal or pelvic fracture 05.History of spinal inflammation or tumor
  • History of osteoporosis.

结局指标

主要结局

Core Strength: Pressure Biofeedback

时间窗: at baseline, 6 weeks and 18 weeks

次要结局

  • Pain(VAS)(Functional Disability (ODI))

研究者

发起方
Department of Physiotherapy and Rehabilitation
申办方类型
Other [University ]
责任方
Principal Investigator
主要研究者

Mohammad Ramiz Uddin

Jashore University of Science and Technology

研究点 (2)

Loading locations...

相似试验