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临床试验/CTRI/2025/09/094752
CTRI/2025/09/094752已完成1 期

SUPER INDUCTIVE SYSTEM (SIS) VERSUS FARADIC FOOT BATH ON PAIN THRESHOLD, PLANTAR PRESSURE AND FOOT POSTURE FOR PLANTAR FASCIITIS: A RANDOMIZED CLINICAL TRIAL

Apeksha C Gore1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年9月30日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
Pain measured by Pain Pressure Algometer

研究概览

简要总结

Super Inductive System vs Faradic Foot Bath on pain threshold ,plantar pressure and foot posture for plantar fasciitis:

A randomized controlled trial.

Objective is to determine and compare the impact of the Super Inductive System versus the Faradic Foot Bath on pain threshold using  a pain pressure algometer,  plantar pressure using Harris Mat, and Foot posture using Foot Posture Index (FPI-6).

A sample size of 40 (20 in each group), aged 20 to 65 years, diagnosed with acute or subacute plantar fasciitis, with a pain score above 3, and willing to participate. Participants with allergies, skin hypersensitivity, open wounds, DVT, rheumatoid arthritis, severe osteoporosis, ankle bursitis, diabetic neuropathy, foot infections, vascular disorders, tumors, impaired circulation, pregnancy, metal implants, epilepsy, psychiatric or cognitive disorders, lower limb fractures, or pacemakers are excluded.

Group A  will receive Super Inductive System therapy (20 minutes per session), and Group B will receive Faradic Foot Bath therapy (15 minutes per session, with timed contractions and rest), both combined with a standardized conventional exercise program (heel raises, ankle dorsiflexion/plantarflexion with resistance band, and foot inversion/eversion with resistance). Sessions will be  held thrice weekly over three weeks.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
20.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Individuals with plantar fasciitis with acute and subacute condition and positive windlass test.
  • Subjects with a pain intensity more than 3.

排除标准

  • Subjects with history of allergic reactions, skin hypersensitivity, open wounds, deep vein thrombosis or skin reactions to the foot and ankle.
  • Individuals diagnosed with rheumatoid arthritis, severe osteoporosis and ankle bursitis.
  • Diagnosed with diabetic neuropathy, foot infection, foot ulcers, vascular disorders, foot tumors, impaired circulation and pregnancy.
  • Subjects with any metal implants, malignant tumors, epilepsy or seizure disorders.
  • Diagnosed with a cognitive and psychiatric disorders.
  • Individuals with lower limb fractures and pacemaker.

结局指标

主要结局

Pain measured by Pain Pressure Algometer

时间窗: Assessed at baseline and post intervention after 3 week Pain measured by Pain Pressure Algometer, Plantar Pressure using Harris Mat and foot posture using foot posture index

Plantar Pressure using Harris Mat

时间窗: Assessed at baseline and post intervention after 3 week Pain measured by Pain Pressure Algometer, Plantar Pressure using Harris Mat and foot posture using foot posture index

foot posture using foot posture index

时间窗: Assessed at baseline and post intervention after 3 week Pain measured by Pain Pressure Algometer, Plantar Pressure using Harris Mat and foot posture using foot posture index

次要结局

  • Foot Posture measured by Foot posture index (FPI -6)(Foot Posture measured by Foot posture index (FPI -6) will be assessed at the baseline and after 3 weeks of the treatment protocol)

研究者

发起方
Apeksha C Gore
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Apeksha C Gore

KAHER Institute of Physiotherapy

研究点 (1)

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