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临床试验/CTRI/2025/07/090936
CTRI/2025/07/090936Not Applicable不适用

Concurrent Validity and Test-Retest Reliability of Ultrasonography-guided Musculoskeletal Evaluation of Non-specific Low Back Pain

Dr Ehsanur Rahman1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年7月23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
60
试验地点
1
主要终点
concurrent validity and test retest reliability

研究概览

简要总结

Nonspecific low back pain is the commonest form of LBP, where the biomechanical abnormalities of the lumbar spine pose abnormal pressure to the muscles, ligaments, and fascial tissues of the lower back. Existing radiological investigations are used only to rule out other causes, so healthcare practitioners manually palpate the paraspinal muscles to diagnose NSLBP. So far, the diagnosis and clinical evaluation of NSLBP is done by patient-reported subjective tools of pain and function. Ultrasonography-guided real-time morphological and clinical evaluation of the muscles, ligaments, fascia, and other soft tissues of the lumbar region might be the future of the diagnosis of specific structural abnormalities in NSLBP. The study objectives are justified to improve the global standard of diagnosis and management for NSLBP regardless of clinical specialty. The musculoskeletal ultrasonography laboratory is fully equipped and functional to conduct the study, and we also have access to a large number of LBP patients at musculoskeletal

outpatient unit in this department.

研究设计

研究类型
Observational

入排标准

年龄范围
20.00 Year(s) 至 40.00 Year(s)(—)
性别
All

入选标准

  • For patients with Low Back Pain (LBP):
  • Age between 20 to 40 years, both male and female.
  • Pain intensity on VAS score between 3 to 7 (moderate pain).
  • X-ray of the lumbar spine showing altered lumbar curvature suggestive of paraspinal muscle spasm.
  • For healthy volunteers (without LBP):
  • No pain or palpable muscle spasm.
  • X-ray of the lumbar spine showing normal findings.

排除标准

  • For patients with low back pain: 1.patients with positive Dural sign and SLUMP test positive 2.patients having SLR positive For healthy volunteers: 1.History of low back pain last six months.

结局指标

主要结局

concurrent validity and test retest reliability

时间窗: 30 days

次要结局

  • Pre & post treatment Reliability of ultrasonography(30 days)

研究者

发起方
Dr Ehsanur Rahman
申办方类型
Other [university]
责任方
Principal Investigator
主要研究者

Sheoshree Roy Dola

Jashore University of Science and Technology

研究点 (1)

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