跳至主要内容
临床试验/NCT06541119
NCT06541119招募中不适用

Effect of Selective Strengthening of Peroneus Longus Muscles on Pain Joint Alignment and Foot Function in Hallux Valgus

Cairo University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
1
主要终点
Hallux valgus angle HVA

研究概览

简要总结

Purpose of this study is to measure Change in Hallux valgus angle (HVA )as measured by kinovea software Change in pain as measured by numerical pain rating scale (NPRS) Change in function as measured by Foot function index (FFI )Egyptian version With the peroneus longus strengthening exercise versus the use of conventional physical therapy programme in cases of hallux valgus patients

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
Double (Participant, Investigator)

盲法说明

Sixty mild to moderate Hallux valgus patients will be evaluated for eligibility ; participants will be randomized in 1:1 ratio using computer generated block randomization , followed by concealed allocation by opening quantity numbered sealed envelopes , a card inside will reveal the group assignment as either group A, or group B.

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • All patients must be diagnosed as having mild to moderate Hallux valgus (with Hallux valgus angle between 15-40 degrees)
  • patients aging between 18-60 .
  • patients must report pain and limited function .
  • patients must report that they are not undergoing physiotherapy , not using orthosis , dynamic splinting exercises for Hallux valgus

排除标准

  • Patients diagnosed with systematic diseases such as rheumatoid arthritis .
  • Cognitive or mental illness.
  • Hallux rigidus or limitus .
  • History of surgery to foot of Hallux .
  • Previous use of foot orthosis .

结局指标

主要结局

Hallux valgus angle HVA

时间窗: Baseline , 6 weeks (after study completion )

Hallux valgus angle will be measures musing kinovea software

Foot function

时间窗: Baseline , 6 weeks after study completion

Will be measured using Foot Function Index FFI Egyptian version Which is divided into 3 sub categories Pain 0 no pain , 10 worst pain Disability 0 least 10 worst Activity limitation 0 no limitation , 10 worst limitation For the total score, the minimum score is 0% (no pain or difficulty), and maximum score is 100% (worst pain and extreme difficulty requiring assistance).

Level of pain

时间窗: Baseline , 6 weeks after study completion

Will be measured using numerical pain rating scale Where 0 represents no pain and 10 represents worst pain imaginable

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

Asmaa Mohamed Kamel Hassan Alminisi

Senior physiotherapist

Cairo University

研究点 (1)

Loading locations...

相似试验