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临床试验/CTRI/2025/06/088574
CTRI/2025/06/088574尚未招募3 期

Effect of Transdermal Magnesium and Moderate Intensity TheraBand Training on Pressure, Pain Threshold, Disability and Quality of Life Among Adults with Sciatic Pain: A Randomized Controlled Trial

Sakshi Vats1 个研究点 分布在 1 个国家目标入组 112 人开始时间: 2025年6月25日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
112
试验地点
1
主要终点
Numeric Pin Rating Scale

研究概览

简要总结

Introduction: Sciatic pain, commonly known as sciatica, is a prevalent condition characterized by radiating pain along the sciatic nerve pathway, significantly affecting an individual’s quality of life due to discomfort, numbness, and muscle weakness.

Aim: To study the effect of transdermal magnesium and moderate intensity TheraBand training on quality of life among adults with sciatic pain. Cost-effective, non-invasive methods of treating sciatic pain are becoming more and more necessary. Investigating the synergistic effects of transdermal magnesium and moderate-intensity TheraBand training may provide an innovative approach to promote integrative pain management techniques by enhancing quality of life, lowering disability, and improving pressure pain threshold in impacted individuals.

Material and Methods: A two-group pretest-post-test randomised clinical trial will be conducted in recognised hospitals in Delhi using simple random sampling from February 2025 to February 2026. Two groups will be formed, each consisting of 56 subjects. Group A will serve as the experimental group receive a transdermal magnesium spray and TheraBand exercises. Group B, the control group, will receive sham transdermal magnesium spray and TheraBand exercises, both groups will be treated for 3 days in a week for 8 weeks. The paired t-test will be employed to assess subjective parameters within the same group, while the unpaired t-test will be used for intergroup comparisons, establishing a significance level of <0.05. This integrated approach addresses both biochemical and functional aspects, offering comprehensive rehabilitation benefits.

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
18.00 Year(s) 至 40.00 Year(s)(—)
性别
All

入选标准

  • 18-40 Years Sciatica Pain Bilateral/Unilateral Disc herniation.

排除标准

  • Surgical Intervention Spinal Infection Spinal Tumor Spinal Fracture Known Mg Deficiency.

结局指标

主要结局

Numeric Pin Rating Scale

时间窗: Numeric Pin Rating Scale (Baseline, 8th week) | Roland Morris Disability Questionnaire (Baseline, 8th week) | SF-36

Roland Morris Disability Questionnaire

时间窗: Numeric Pin Rating Scale (Baseline, 8th week) | Roland Morris Disability Questionnaire (Baseline, 8th week) | SF-36

SF-36

时间窗: Numeric Pin Rating Scale (Baseline, 8th week) | Roland Morris Disability Questionnaire (Baseline, 8th week) | SF-36

次要结局

  • Serum Electrolyte Level(Baseline, 8th week)

研究者

发起方
Sakshi Vats
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Sakshi Vats

GALGOTIAS University

研究点 (1)

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