Comparison of the Effects of Low-Level Therapy Laser and Orthotic Insole on Pain, Function and Muscle Strength in Subjects With Stage 1-2 Tibialis Posterior Tendon Insufficiency: Randomized Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 52
- 试验地点
- 2
- 主要终点
- Change in Foot Function Assesed With Foot Function Index
研究概览
简要总结
The purpose of this study is to compare low-level laser therapy and insole interventions on pain, function and muscle strength in subjects with posterior tendon insufficiency.
详细描述
Purpose of the research; stage 1-2 tibialis between the ages of 18-60 is a comparison of low-level laser therapy and orthotic insole on pain, function and muscle strength in subjects with posterior tendon insufficiency.
Type of research:
This study is a randomized comparative intervention study.
Place to do research:
The study will be carried out in the Prosthetic Orthotics and Biomechanics Center of the Department of Physiotherapy and Rehabilitation of the Faculty of Health Sciences of the Eastern Mediterranean University.
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
- None
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Taking the diagnosis of stage 1 - 2 tibialis posterior insufficiency by the physician,
- •Be between the ages of 18 and 60,
- •The absence of a different orthopedic or neurological disease that may affect the lower extremity biomechanics,
- •Not having a systemic disease that keeps feet.
- •Having not received any treatment from the foot area in the last 1 year.
排除标准
- •Having lower extremity discrepancy more than 1 centimeter (cm),
- •Having no ambulation without help.
研究组 & 干预措施
Orthotic Insole
Device: Orthotic Insole 8-week follow-up with Orthotic Insole
干预措施: Orthotic Insole (Device)
Low-level Laser Therapy
Low-Level Laser 5-week follow-up
干预措施: Low-Level Laser (Device)
结局指标
主要结局
Change in Foot Function Assesed With Foot Function Index
时间窗: Baseline and 6 week for Low-Level Laser Therapy Group - 8 week for Orthotic Insole Group
This scale evaluates the severity of foot pain in different situations. It consists of 3 subtitles and contains 23 questions in total. Turkish version adaptation study is done, valid and reliable measure. The total score obtained by the patient between 0-10 of each question was scaled by obtaining a score of 100 with the number of answered questions
次要结局
- Change in Muscle Strength Assesed With Humac Norm Isocynetic Dynanometer(Basline and 6 week for Low-Level Laser Therapy Group - 8 week for Orthotic Insole Group)
- Change in Foot Pain Assesed With Digital Algometer(Baseline and 6 week for Low-Level Laser Therapy Group - 8 week for Orthotic Insole Group)
研究者
Cansu Koltak
Research Assistant
Eastern Mediterranean University