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临床试验/NCT06913413
NCT06913413进行中(未招募)不适用

Effects Of 8-Week Core Stabilization Exercise With Vitamin D On Pain and Functional Limitation in Adults With Chronic Non-Specific Low Back Pain

Superior University1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2025年3月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
52
试验地点
1
主要终点
The Visual Analogue Scale (VAS)

研究概览

简要总结

Chronic non-specific low back pain (CNSLBP) is a prevalent condition contributing to pain, functional limitations, and reduced quality of life. Core stabilization exercises (CSE) have shown promise in enhancing spinal stability and reducing symptoms. Additionally, vitamin D supplementation plays a critical role in musculoskeletal health. Study objective will be to determine combined effect of vitamin D supplementation and core Stabilization exercises is better than core Stabilization Exercises alone in reducing pain-related and functional independence among chronic non-specific low back patient A randomized controlled trial will be conducted on 52 adults aged 25-45 diagnosed with Chronic non-specific low back pain.

详细描述

Subjects will be divided into two groups: the intervention group will receive an 8-week Core stabilization exercises program alongside daily vitamin D supplementation, while the control group will receive either Core stabilization exercises alone Visual Analog Scale (VAS), and Oswestry Disability

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
25 Years 至 40 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Adults aged 25 to 45 years will be included.
  • •Both gender Male /Female will participate.
  • •Subjects with diagnosed non-specific low lumber pain persisting for at least 12 weeks will be included.
  • •Subjects must have baseline pain score of ≥4 on the Visual Analog Scale.
  • •Confirmed serum vitamin D levels <30 ng/m will be included

排除标准

  • •Low lumber pain due to specific causes such as fracture malignancy infection or inflammatory diseases (e.g. ankylosing spondylitis).
  • •Presence of significant comorbidities that could interfere with participation (e.g. cardiovascular neurological or respiratory disorders).
  • •History of spinal surgery within the last year.
  • •Subjects currently taking vitamin D supplements or undergoing other treatments for vitamin D deficiency.
  • •Use of medications such as corticosteroids or opioids that might affect pain perception or functional assessment.
  • •Enrolled in any other physical therapy or pain management program within the last three months.

研究组 & 干预措施

core stabilization exercise

Experimental

干预措施: core stabilization exercise (Combination Product)

stabilization exercise

Active Comparator

干预措施: stabilization exercise (Diagnostic Test)

结局指标

主要结局

The Visual Analogue Scale (VAS)

时间窗: 12 Months

The Visual Analogue Scale (VAS) uses a 10 cm line with anchors like "no pain" and "worst pain imaginable", and the score is determined by measuring the distance (in mm or cm) from the "no pain" end to the patient's mark, ranging from 0 to 100

The Oswestry Disability Index (ODI)

时间窗: 12 Months

The Oswestry Disability Index (ODI) is a questionnaire used to assess functional disability in individuals with low back pain, with scores ranging from 0% (no disability) to 100% (maximum disability), and interpreted as follows: 0-20% minimal disability, 21-40% moderate, 41-60% severe, 61-80% crippling, and 81-100% bed-bound or exaggerated symptoms

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

Muhammad Naveed Babur

Principal Investigator

Superior University

研究点 (1)

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