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临床试验/NCT06918158
NCT06918158已完成不适用

Comparative Study on the Effectiveness of Mobilization With Movement Versus Joint Specific Manipulation on Pain and Function in Patient With Dequervains Tenosynovitis

Riphah International University2 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2025年2月17日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
32
试验地点
2
主要终点
Pain Reduction - Measured using the Numeric Pain Rating Scale (NPRS) (0-10 scale).

研究概览

简要总结

A comparative study on the effectiveness of mobilization with movement (MWM) versus joint-specific manipulation (JSM) in patients with De Quervain's tenosynovitis typically aims to assess how each technique impacts pain relief and functional improvement. De Quervain's tenosynovitis is an inflammation of the tendons around the thumb and wrist, often causing pain, swelling, and difficulty in performing everyday tasks. The study would likely compare the two interventions by measuring pain levels, range of motion, and overall functional outcomes before and after treatment. MWM involves applying specific, controlled movements while the patient is actively engaging in their joint motion, targeting the tissue's mobility and reducing pain. JSM, on the other hand, focuses on manipulating the joint directly to restore normal function, specifically targeting the wrist and thumb regions affected by the condition.

详细描述

A comparative study on the effectiveness of Mobilization with Movement (MWM) versus Joint-Specific Manipulation (JSM) in patients with De Quervain's Tenosynovitis would delve deeper into the physiological mechanisms and clinical outcomes associated with each technique, providing valuable evidence for therapeutic decision-making. De Quervain's Tenosynovitis is a condition characterized by the inflammation of the tendons at the base of the thumb, particularly affecting the abductor pollicis longus and extensor pollicis brevis tendons. This condition is commonly caused by repetitive strain, overuse, or trauma, leading to pain, swelling, and restricted movement, which significantly impacts the patient's daily activities.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Health Services Research
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • o Patients clinically diagnosed with De Quervain's tenosynovitis
  • Age between 25-45 years.
  • Positive Finkelstein test.
  • Pain over the first dorsal compartment.
  • Limited wrist and thumb function.
  • Willingness to take part and adhere to the study's guidelines.

排除标准

  • Participants fall in this category would be excluded of the study.
  • Previous surgery of wrist or thumb.
  • Presence of neurological symptoms like numbness, weakeness.
  • Rheumatological conditions like rheumatoid arthritis.
  • Pregnancy.
  • Presence of wrist fracture or osteoporosis.
  • Carpel tunnel syndrome.

结局指标

主要结局

Pain Reduction - Measured using the Numeric Pain Rating Scale (NPRS) (0-10 scale).

时间窗: 6 Months

Pain intensity will be assessed using the Numeric Pain Rating Scale (NPRS), a validated tool where participants rate their pain on a scale from 0 no pain to 10 worst possible pain.

次要结局

  • Wrist Function - Assessed with the Patient-Rated Wrist Evaluation (PRWE) (0-100 scale).(6months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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