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临床试验/NCT06677164
NCT06677164已完成不适用

Gluteus Maximus Strengthening Exercises Augmented by High-Intensity Laser Therapy in Patients With Chronic Plantar Fasciopathy

Deraya University1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2024年3月10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
入组人数
100
试验地点
1
主要终点
Pain assessment

研究概览

简要总结

Plantar heel pain is one of the most commonly encountered problems of the feet in adults [1]. It accounts for nearly 11%-15% of all foot symptoms, The purpose of this study was to investigate the effectiveness of high intensity laser therapy combined with gluteus Maximus strengthening exercise on pain, thickness of plantar fascia, and function of the foot.

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
Single (Participant)

盲法说明

single

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Unilateral plantar heel pain with or without calcaneal spur for more than 3 months.
  • •Tenderness at the insertion of the plantar fascia
  • •BMI index will be from 25 up to 30
  • •Patient will wear silicone insole .
  • •Diagnosis of PF based on orthopedic referral

排除标准

  • •Patients with presence of foot deformity,
  • •systemic inflammatory arthritis disease,
  • •foot surgery, or
  • •plantar heel pain due to trauma,
  • •wound, or infection in the foot,
  • •received oral corticosteroids

研究组 & 干预措施

Experimental: High intensity laser therapy combined with Gluteus Maximus strengthening exercise

Experimental

patients will receive High intensity laser therapy combined with Gluteus Maximus strengthening exercise

干预措施: Gluteus Maximus strengthening exercise (Procedure)

Experimental: High intensity laser therapy combined with Gluteus Maximus strengthening exercise

Experimental

patients will receive High intensity laser therapy combined with Gluteus Maximus strengthening exercise

干预措施: high-intensity laser therapy (Device)

Active Comparator: High intensity laser therapy

Active Comparator

patients will receive High intensity laser therapy.

干预措施: high-intensity laser therapy (Device)

结局指标

主要结局

Pain assessment

时间窗: 3 months

Pressure algometry (kg/cm2). Pressure algometry will be performed on both affected and healthy feet

Plantar fascia thickness

时间窗: 3 months

by using Ultrasonography, in a longitudinal view of the tendon in both affected and healthy feet (mm). the normal plantar fascia thickness is less than 4 mm

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Soad Ali

associate professor

Deraya University

研究点 (1)

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