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临床试验/CTRI/2025/08/093825
CTRI/2025/08/093825尚未招募不适用

Comparison between dry needling and ischemic compression therapy in non-specific fascio- thoracic pain among young adults.

Diksha Solanki1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年9月15日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
80
试验地点
1
主要终点
Pain

研究概览

简要总结

The research proposal titled “Comparison between Dry Needling and Ischemic Compression Therapy in Non-Specific Fascio-Thoracic Pain among Young Adults” by focuses on evaluating and comparing the effectiveness of two physiotherapy interventions for managing thoracic fascia-related pain. Non-specific fascio-thoracic pain, often associated with myofascial trigger points, poor posture, and muscular imbalances, is a common clinical problem in young adults. The study aims to assess the impact of dry needling and ischemic compression therapy on pain reduction, pressure pain threshold, and trigger point release. Conducted as an experimental study with 80 participants aged 18–40 years, it will involve dividing subjects into two groups: one receiving dry needling at specific thoracic paraspinal levels and the other undergoing ischemic compression at active trigger points. Pain will be measured using the Numeric Pain Rating Scale, and pressure pain threshold will be assessed with an algometer. By directly comparing these two interventions, the study seeks to determine which technique provides greater effectiveness in alleviating fascio-thoracic pain and improving functional outcomes.

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

  • Subjects with non-specific fascio- thoracic pain.
  • Both male and female subjects aged between 18- 40 years
  • History of thoracic pain
  • Subjects with a hypersensitive nodule within a palpable taut band of skeletal muscle.

排除标准

  • Subjects on anti-coagulant or anti-aggregate medications
  • History of systemic or local infection
  • History of heart surgery in past 6 months
  • History thoracic rib and thoracic spine fracture
  • Subjects suffering from malignancy
  • Subjects having fear of needles.

结局指标

主要结局

Pain

时间窗: 2 weeks

Height

时间窗: 2 weeks

Weight

时间窗: 2 weeks

Pressure pain threshold

时间窗: 2 weeks

次要结局

未报告次要终点

研究者

发起方
Diksha Solanki
申办方类型
Other [myself]
责任方
Principal Investigator
主要研究者

Diksha Solanki

Guru Nanak Dev University

研究点 (1)

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