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临床试验/NCT07580430
NCT07580430已完成不适用

Comparing The Effects of Gong's Mobilization and Jone's Positional Release for Sacroiliac Joint Dysfunction.

Elite College of Management Sciences, Gujranwala, Pakistan1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30
试验地点
1
主要终点
Modified Oswestry Low Back Pain Disability Questionnaire

研究概览

简要总结

This study aims to compare the efficacy of Gong's mobilization and Jones's positional release technique in individuals with sacroiliac joint dysfunction.

详细描述

The study was designed as a randomized controlled trial involving 30 participants diagnosed with sacroiliac joint dysfunction. Participants were randomly divided into two equal groups of 15 using a lottery method. Group A underwent Gong's mobilization, whereas Group B received Jones's positional release technique. In addition, both groups were provided with baseline treatment, including TENS and stretching exercises. Each intervention was carried out three times per week for a duration of six weeks.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

性别
All
接受健康志愿者

入选标准

  • Positive provocation tests
  • Low Back and Buttocks pain for more than 3 months
  • Oswestry score of atleast thirty percent

排除标准

  • Spinal fracture
  • Lower extremity fracture
  • pregnancy
  • spinal deformity

研究组 & 干预措施

Gong's mobilization

Experimental

A pain-free, sustained glide is applied to the sacroiliac joint by the therapist. The patient simultaneously performs active movements.

干预措施: Gong's mobilization (Other)

Jone's positional release

Experimental

The therapist identifies a tender point. The patient is positioned in a way that reduces pain significantly. This position is held for about 90 seconds and the patient is then slowly returned to a neutral position.

干预措施: Jone's positional release (Other)

结局指标

主要结局

Modified Oswestry Low Back Pain Disability Questionnaire

时间窗: 6 weeks

The Modified Oswestry Low Back Pain Disability Questionnaire is a gold-standard tool used to measure a patient's functional disability level resulting from low back pain.

Visual Analogue Scale

时间窗: 6 weeks

The Visual Analogue Scale (VAS) is used to measure pain intensity. The VAS typically consists of a 100 mm (10 cm) horizontal line where zero means no pain and ten indicates worst possible pain.

次要结局

未报告次要终点

研究者

发起方
Elite College of Management Sciences, Gujranwala, Pakistan
申办方类型
Other
责任方
Sponsor

研究点 (1)

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