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

Not Applicable

Recruiting

• Conditions: Hallux Valgus

• Registration Number: NCT06541119
• Lead Sponsor: Cairo University

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Status Verified: 2024-08
• Study First Submitted: 2024-08-02
• Study First Submitted QC: 2024-08-02
• Study First Posted: 2024-08-07
• Last Update Submitted: 2024-08-09
• Last Update Posted: 2024-08-12
• Study Start: 2024-09-01
• Primary Completion: 2024-11-01
• Study Completion: 2024-11-15

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• 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

Exclusion Criteria

• 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 .

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Hallux valgus angle HVA	Baseline , 6 weeks (after study completion )	Hallux valgus angle will be measures musing kinovea software
Level of pain	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
Foot function	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).

Trial Locations

Locations (1)

Cairo university; 🇪🇬 Giza, Egypt