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Not yet recruiting NCT07409974

Immediate Effect of Taping on Foot Biomechanics in Patients With 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: rigit taping, kinesiologic taping.
Who it may be relevant to
Registry conditions: Hallux Valgus. Basic parameters: 18 years — 65 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
Turkey (Türkiye)
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

Comparison of the Immediate Effects of Kinesiological and Rigid Taping on Foot Biomechanics in Patients With Hallux Valgus

Overview

The goal of this clinical trial is to comparatively investigate the immediate effects of rigid taping and kinesiological taping applications on foot biomechanics in patients with hallux valgus (HV). The main questions it aims to answer are: Which taping approach (rigid or kinesiology) produces the most effective and fastest treatment response in the management of hallux valgus? Researchers will compare two taping methods to investigate which method offers a more effective and faster treatment response in terms of foot biomechanics. Participants will: 1. Individuals aged 18-65 years 2. Individuals with mild to moderate HV in one or both feet 3. HV patients who do not require/are not suitable for surgery or who refuse surgery and are referred/apply for conservative treatment 4. Individuals who have not engaged in any strenuous exercise or activity (such as running, walking, weight or resistance training, yoga, pilates, aerobics, step, etc.) in the last 2 days before evaluation.

Interventions

  • Other rigit taping
    rigit taping technique
  • Other kinesiologic taping
    kinesiologic taping technique

Primary outcome measures

  • Pedobarogaphic parameters [Time frame: Day 1]

Eligibility criteria

Inclusion criteria

  • Individuals aged 18-65 years
  • Individuals with mild to moderate HV in one or both feet
  • HV patients who do not require/are not suitable for surgery or who refuse surgery and are referred/apply for conservative treatment
  • Individuals who have not engaged in any strenuous exercise or activity (such as running, walking, weight or resistance training, yoga, pilates, aerobics, step, etc.) in the last 2 days before evaluation.

Exclusion criteria

  • The presence of contraindications for the use of the tapes (skin lesions, wounds, fungal infections, allergic reactions, sensory loss, etc.).
  • Diagnosis of diabetic foot.
  • Complete loss of hallux mobility, presence of interdigital neuroma, excessive pain and tenderness during mobility.
  • Foot posture in advanced pronation or supination.
  • The presence of diseases or problems that may affect gait (necessity of using a walking aid, visual or hearing impairment, other problems related to the lower extremity or spine).
  • Having experienced orthopedic trauma or surgery involving the lower extremity.
  • The presence of severe shortness of breath or inability to tolerate walking while walking.
  • The person's; 9. Having a medical history that increases the risk of falls, such as unexplained fainting, blood sugar imbalance, unstable low or high blood pressure.

10\. Having an orthopedic or rheumatological disease (rheumatoid arthritis, gout, etc.) or a systemic disease associated with diabetes or connective tissue disorder.

11\. Being pregnant or in the first 6 months postpartum. 12. Having cooperation problems to the extent that one cannot understand and comply with the assessment protocols.

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
Single blind
Primary purpose
Screening

Study locations

Turkey (Türkiye) · 1 center
  • Pınar Kısacık — Ankara

Identifiers

NCT: NCT07409974 · FTREK24/93

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗