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Recruiting NCT06541119

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

No phase Interventional Hallux Valgus

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Selective Peroneus longus excercise, Conventional physical therapy programme.
Who it may be relevant to
Registry conditions: Hallux Valgus. Basic parameters: 18 years — 60 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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

Interventions

  • Other Selective Peroneus longus excercise
    Weight bearing peroneus longus exercise
  • Other Conventional physical therapy programme
    * Passive abduction of the Hallux with traction * short foot exercise * toe spread outs

Primary outcome measures

  • Hallux valgus angle HVA [Time frame: Baseline , 6 weeks (after study completion )]
  • Level of pain [Time frame: Baseline , 6 weeks after study completion]
  • Foot function [Time frame: Baseline , 6 weeks after study completion]

Eligibility criteria

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 .

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Cairo university — Giza

Identifiers

NCT: NCT06541119 · 012/005050

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗