Effect of Neural Mobilization Techniques on Pain, and Hip and Knee Range of Motion on Lumbosacral Radiculopathy Patients With Peripheral Sensitization
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 51
- 主要终点
- Knee Flexion Range of Motion (Symptomatic Side)
研究概览
简要总结
The primary purpose of this study was to investigate the effects of slider and tensioner techniques on pain, hip and knee ROM in lumbosacral radiculopathy patients with peripheral sensitization. A secondary purpose was to evaluate the correlation between these outcomes measurements.
详细描述
Study design: Double-blind case-control trial. Methods: Fifty-one male lumbosacral radiculopathy patients with peripheral sensitization, were divided into one of the three groups: slider, tensioner, and control. The primary outcome measurements were visual analog scale (VAS) for pain, hip range of motion (ROM) during SLR test, and knee flexion ROM during slump test. The measurements were taken at baseline, after 1st, 3rd, and 6th session.
Statistical Analysis
A two-way mixed design analysis of variance (MANOVA) with post-hoc (Bonferonni Correction) was used to calculate the differences with Time (baseline, 1st,3rd,6th sessions) as a within-group factor and Group (control, slider, and tensioner) as a between-group factor. The effect size was calculated with Cohen's d. Pearson's correlation was used for correlation analysis.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Care Provider, Outcomes Assessor)
盲法说明
both the examiner and the outcomes assessor where blinded to the participants groups. the primary investigator was also blind to the outcomes of each participant during the study period.
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •Patients with lumbosacral radiculopathy with dominant peripheral sensitization
- •patients with unilateral leg pain.
- •patient S-LANSS score > 12,
- •negative sensory and motor examination.
- •positive neural tissue provocation tests (straight leg raising test, slump test).
- •pain duration of more than 3 months.
排除标准
- •S-LANSS score ≥ 12,
- •motor or sensory deficits,
- •history of back or lower extremity surgeries,
- •bilateral referred pain,
- •patients with pacemakers, cardiovascular problems, epilepsy, active malignancy, dermatological conditions, and diminished pain sensation.
结局指标
主要结局
Knee Flexion Range of Motion (Symptomatic Side)
时间窗: The measurements were taken at days "0,1,5,12"
Change in Knee flexion range of motion during slump (symptomatic side)
Hip Flexion Range of Motion (Asymptomatic Side)
时间窗: The measurements were taken at days "0,1,5,12"
Change in Hip Flexion Range of Motion During Straight Leg Raising (Asymptomatic Side)
Knee Flexion Range of Motion (Asymptomatic Side)
时间窗: The measurements were taken at days "0,1,5,12"
Change in Knee flexion range of motion during slump (Asymptomatic side)
Visual Analog Scale
时间窗: The measurements were taken at days "0,1,5,12"
Visual analog scale was used to measure pain intensity. This scale is a 10 cm line where patients chose from 0 to 10 (when 0 mean no pain and 10 mean maximum pain)
Hip Flexion Range of Motion (Symptomatic Side)
时间窗: The measurements were taken at days "0,1,5,12"
Change in Hip flexion range of motion during straight leg raising (symptomatic side)
次要结局
未报告次要终点
研究者
Mohammed Al-Ghamdi
Physical Therapist
Imam Abdulrahman Bin Faisal University