跳至主要内容
临床试验/NCT05347940
NCT05347940Unknown不适用

EFFICACY OF MIRROR THERAPY IN IMPROVING HAND FUNCTION POST FLEXOR TENDON REPAIR

Cairo University2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2022年6月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
30
试验地点
2
主要终点
pain assessment

研究概览

简要总结

This current study will be designed to prove the therapeutic effect of mirror therapy on physical function of the hand after flexor tendon repair

详细描述

Purpose of the study are to clarify the effectiveness of mirror therapy (MT) on pain, range of motion and hand function in post tendons repair patients. 30 adult of both sexes will participate in this study and selected from outpatient clinic of faculty of physical therapy Cairo university. Their ages range from 20 to 45 years.

Informed consent will be taken from all patients. All the adult were divided into two groups of equal number (15) Study group (A): received traditional physical therapy program in addition to motor imagery in form of mirror therapy.

Study group (B): received traditional physical therapy program only.

Procedures of the study:

  • A verbal explanation about the importance of this study procedures, main aims and conceptual approach were explained to every patient.
  • The procedures of this study will be divided into two main categories:

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 (Outcomes Assessor)

入排标准

年龄范围
20 Years 至 45 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age 20-45 Males and females Flexor tendons repair All patients enrolled to the study will have their informed consent.

排除标准

  • •Open fractures Associated vascular injury Cruch injuries Cognitive disorders

研究组 & 干预措施

Study group (A)

Experimental

Study group (A):15 patient received traditional physical therapy program in addition to motor imagery in form of mirror therapy.

干预措施: mirror therapy (Other)

Study group (B)

Experimental

Study group (B):15 patient received traditional physical therapy program only.

干预措施: traditional physiotherapy protocol for flexor tendon repair (Other)

结局指标

主要结局

pain assessment

时间窗: 8 weeks

pain assessment using Visual analog scale

Active ROM

时间窗: 8 weeks

Active ROM of the finger with repaired tendon using Standard geniometer

Hand function

时间窗: 8 weeks

Hand function using Michigan Hand Questionnaire

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

ahmed mohamed nagy

lecturer of physical therapy for surgery- cairo university

Cairo University

研究点 (2)

Loading locations...

相似试验