The Efficacy of Sacroiliac Joint Mobilization on Pain, Function and Disability in Patient with Lumbar Prolapse Intervertebral Disc.
概览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- Aarunee Srivastava
- 入组人数
- 45
- 试验地点
- 1
- 主要终点
- 1. Visual Analog Scale (VAS)
概览
简要总结
The lumbar-pelvic-hip complex, including the sacroiliac joint (SIJ), constitutes an interconnected anatomical unit. Dysfunctions within one region can often manifest as symptoms in others. Extensive research has established a significant association between lumbar prolapsed intervertebral disc (PIVD), a prevalent cause of low back pain, and SIJ abnormalities. Notably, up to 30.7% of individuals presenting with sciatica and low back pain exhibit concomitant SIJ dysfunction. While SIJ mobilization offers a promising therapeutic approach, further rigorous investigation is imperative to elucidate its efficacy for lumbar PIVD, particularly considering the potential risks associated with spinal and SIJ manipulation in this patient population. To find the efficacy of SIJ mobilization on pain, function and disability in patients with lumbar prolapse intervertebral disc. A total of 45 participants will be recruited based on predefined inclusion and exclusion criteria. A single-group, pre-test-post-test quasi-experimental design will be employed. Participants will receive SI joint mobilization utilizing a postero-anterior glide technique and lumbar extension, in conjunction with core muscle strengthening exercises. Pre- and post-intervention assessments will be conducted using the Visual Analogue Scale, Timed Up and Go Test, and the Oswestry Disability Index. Data Normality will be assessed using the Shapiro-Wilk test. For normally distributed data, paired t-tests will be used to analyze within-group differences. If the data is not normally distributed, the Wilcoxon Signed-Rank test will be used for within-group comparisons. This research aligns with a patient-centered approach, fostering a deeper understanding of the efficacy of SIJ mobilization on pain, function, and disability in patients with lumber PIVD.
研究设计
- 研究类型
- Interventional
- 分配方式
- Not Applicable
- 盲法
- Not Applicable
入排标准
- 年龄范围
- 30.00 Year(s) 至 50.00 Year(s)（—）
- 性别
- All
入选标准
- •Participants must be between 30 and 50 years of age.
- •Both male and female participants are eligible.
- •Acute cases of PIVD, that is onset in less than three months will be considered.
- •Unilateral lumbar PIVD, as confirmed by MRI findings, will be considered.
- •Only paracentral, foraminal, and extraforaminal disc bulges or prolapses will be included;
- •Participants must exhibit unilateral radiating pain without associated motor or sensory deficits.
排除标准
- •Participants younger than 30 years or older than 50 years will be excluded.
- •Chronic cases of PIVD, that are diagnosed for more than 3 months will be excluded.
- •Central bulges, Extruded or sequestrated discs, and spinal stenosis will be excluded.
- •Low back pain due to any other cause.
- •Individuals with motor or sensory deficits will be excluded.
- •Individuals who have undergone any physiotherapy or surgical intervention to address lumbar PIVD in the last 3 months.
结局指标
主要结局
1. Visual Analog Scale (VAS)
时间窗: At: | 1. Pre-intervention (Immediately after recruitment) | 2. Post-intervention (After 6 sessions of intervention)
2. Time Up and Go test (TUG)
时间窗: At: | 1. Pre-intervention (Immediately after recruitment) | 2. Post-intervention (After 6 sessions of intervention)
3. Oswestry Disability Index (ODI)
时间窗: At: | 1. Pre-intervention (Immediately after recruitment) | 2. Post-intervention (After 6 sessions of intervention)
次要结局
未报告次要终点