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Clinical Trials/NCT07177768
NCT07177768Not yet recruitingNot Applicable

Acute Effects of Prolonged Walking on Pain, Balance and Posture in Individuals With Hallux Valgus Deformity

Bezmialem Vakif University1 site in 1 country32 target enrollmentStarted: October 1, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
32
Locations
1
Primary Endpoint
Pain intensity

Study Overview

Brief 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.

Detailed Description

Hallux valgus is a progressive foot deformity commonly seen in adults. Patients typically report pain, most prominently in the first metatarsophalangeal joint, which is often exacerbated by weight-bearing activities such as walking. Due to the deformity, alterations in plantar pressure distribution occur, which in turn affect plantar sensory input and postural control. This may lead to decreased postural stability, impaired balance, and compromised control during walking. HV is also thought to accelerate biomechanical changes that negatively impact gait patterns. The aim of this study is to evaluate the acute effects of prolonged walking on pain, balance, posture, and gait in individuals with hallux valgus deformity. A total of 32 participants, including individuals with HV and healthy controls, will be included in the study. All participants will walk on a treadmill for 60 minutes. Assessments will be conducted at three time points: before walking, immediately after walking, and 20 minutes post-walking.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to 55 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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

Arms & Interventions

Hallux Valgus Group

Experimental

Individuals with hallux valgus deformity

Intervention: Prolonged walking (Other)

Control Group

Other

Healthy controls

Intervention: Prolonged walking (Other)

Outcomes

Primary Outcomes

Pain intensity

Time Frame: 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

Time Frame: 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

Time Frame: 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

Time Frame: 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

Time Frame: 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.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Kübra Alpay

Lecturer of Pysiotherapy and Rehabilitation Department

Bezmialem Vakif University

Study Sites (1)

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