NCT07177768

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
32

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 10, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

September 17, 2025

Completed
14 days until next milestone

Study Start

First participant enrolled

October 1, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2026

Completed
Last Updated

September 17, 2025

Status Verified

September 1, 2025

Enrollment Period

5 months

First QC Date

September 10, 2025

Last Update Submit

September 10, 2025

Conditions

Outcome Measures

Primary Outcomes (5)

  • Pain intensity

    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.

    Baseline, immediately after intervention, 20 minutes after intervention

  • Pressure pain threshold

    It will be measured with algometer. Higher values indicate a higher perceived pain threshold.

    Baseline, immediately after intervention, 20 minutes after intervention

  • Single-leg stance test

    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.

    Baseline, immediately after intervention, 20 minutes after intervention

  • Postural Assessment

    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.

    Baseline, immediately after intervention, 20 minutes after intervention

  • Gait analysis

    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.

    Baseline, immediately after intervention, 20 minutes after intervention

Study Arms (2)

Hallux Valgus Group

EXPERIMENTAL

Individuals with hallux valgus deformity

Other: Prolonged walking

Control Group

OTHER

Healthy controls

Other: Prolonged walking

Interventions

walking on a treadmill for 60 minutes

Control GroupHallux Valgus Group

Eligibility Criteria

Age18 Years - 55 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • History of previous foot or ankle surgery
  • Having a systemic diseases
  • Having a neurological disorders
  • Having a vestibular pathologies that may affect balance

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bezmialem Vakif University

Istanbul, Eyup, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Hallux Valgus

Condition Hierarchy (Ancestors)

Foot DeformitiesMusculoskeletal Diseases

Study Officials

  • Ozgur Serbest, Pt

    Bezmialem Vakif University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer of Pysiotherapy and Rehabilitation Department

Study Record Dates

First Submitted

September 10, 2025

First Posted

September 17, 2025

Study Start

October 1, 2025

Primary Completion

March 1, 2026

Study Completion

April 1, 2026

Last Updated

September 17, 2025

Record last verified: 2025-09

Locations