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Starting soon Not applicable

Acute Effects of Prolonged Walking on Hallux Valgus

NCT07177768 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-10
Last updated
2025-09-17

Condition(s) studied

Hallux Valgus

Investigational drug(s) / intervention(s)

Prolonged walking

Prolonged walking: walking on a treadmill for 60 minutes

Study summary

Hallux valgus is a progressive foot deformity characterized by lateral deviation of the great toe and medial displacement of the first metatarsal head. While pain is a common symptom among individuals with HV, alterations in plantar pressure distribution and impaired balance are also frequently observed. These symptoms and biomechanical changes can negatively impact posture and gait mechanics. The aim of this study is to investigate the acute effects of prolonged walking on pain, balance, posture, and gait in individuals with hallux valgus deformity.

Eligibility

Sex
ALL
Min age
18 Years
Max age
55 Years
Healthy volunteers
Accepted
Inclusion Criteria: Hallux Valgus Group Criteria: * Individuals aged between 18 and 55 years * Being diagnosed with hallux valgus Control Group Criteria: * Individuals aged between 18 and 55 years * Classified as grade A according to the Manchester Scale * Being a volunteer Exclusion Criteria: * History of previous foot or ankle surgery * Having a systemic diseases * Having a neurological disorders * Having a vestibular pathologies that may affect balance

Primary outcome measure(s)

  • Pain intensity — Baseline, immediately after intervention, 20 minutes after intervention
    Pain intensity will be evaluated with visual analog scale (VAS). Patients will be asked to mark the intensity of the pain they feel on a 10 cm line, where "0" means no pain and "10" means the worst pain.
  • Pressure pain threshold — Baseline, immediately after intervention, 20 minutes after intervention
    It will be measured with algometer. Higher values indicate a higher perceived pain threshold.
  • Single-leg stance test — Baseline, immediately after intervention, 20 minutes after intervention
    The single leg stability will be assessed by using Biodex Balance System® (Biodex Medical Systems, Inc. USA). Low values of the stability index indicate better balance and stability.
  • Postural Assessment — Baseline, immediately after intervention, 20 minutes after intervention
    Posture will be assessed using mobile application. It marks and measures angles at the ear, shoulder, anterior superior iliac spine (ASIS), knee, and ankle alignment to identify any pathological deviations or asymmetries.
  • Gait analysis — Baseline, immediately after intervention, 20 minutes after intervention
    Gait analysis will be performed using mobile application. Subjects are asked to walk at their normal walking speed over a 10-meter surface, and measurements are taken using video recording and evaluated using the software. The assessment records right and left step lengths, double step length, stride width, and walking speed.

Trial sites (1)

FacilityCityRegionStatus
Bezmialem Vakif University Istanbul Eyup
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07177768 on ClinicalTrials.gov ↗ ← All trials in Turkey