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临床试验/CTRI/2026/02/104613
CTRI/2026/02/104613尚未招募不适用

Efficacy of Instrument Assisted Soft Tissue Mobilization (IASTM) Versus High Intensity Laser Therapy (HILT) on Pain, Foot functions and Activity Limitations in patients with Plantar fasciitis.

未提供1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2026年3月9日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
40
试验地点
1

研究概览

简要总结

This study is a randomised clinical trial, subjects with plantar fasciitis will be screened based on inclusion and exclusion criteria. Those who meet the criteria will be enrolled after completing clinical assessment, demographic data recording, and obtaining informed consent. A total of 40 subjects will be randomly divided into two groups of 20 each. One group will receive Instrument Assisted Soft Tissue Mobilization (IASTM) along with standardized exercises, while the other group will receive High Intensity Laser Therapy (HILT) with the same exercise program. The intervention will be carried out for 4 weeks. Study parameters will be assessed at baseline and again after 4 weeks to compare pre- and post-treatment outcomes.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
25.00 Year(s) 至 45.00 Year(s)(—)
性别
All

入选标准

  • Age-range: 25-45 years.
  • Both males or females.
  • Patient with painful tender heel.
  • Pain that worsened in the morning and after prolonged standing or walking.
  • NPRS score of more than or equal to
  • Exacerbation of local pain on plantar fascia stretch around medial tubercle of calcaneum.

排除标准

  • Systematic inflammatory diseases.
  • Previous fracture or surgery of the foot.
  • Rheumatoid arthritis.
  • Diabetes mellitus.
  • Osteoporosis.
  • Cancer, infectious disease and tumor.
  • Calcaneal spur showing on radiological finding will be excluded.
  • Patient with Navicular drop of 10mm or more will be excluded.

研究者

发起方
未提供
责任方
Principal Investigator
主要研究者

Dr Bhagya Laxmi Uikey PT

Pandit. Deendayal Upadhyaya National Institute for Person with Physical Disabilities (Divyangjan)

研究点 (1)

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