Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
All Genders
ID07286773

Evaluation of the Effectiveness of Biofeedback-Assisted Short Foot Exercises in Individuals With Flexible Pes Planus: A Randomized Controlled Trial

Led by Istanbul University - Cerrahpasa · Updated on 2026-02-06

30

Participants Needed

2

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of biofeedback-assisted short foot exercises compared to traditional short foot exercises in adults with flexible pes planus, also known as flexible flatfoot. The study aims to find out if adding biofeedback to exercises improves foot biomechanics, balance, and functional ability more than exercises alone. The research will focus on changes in plantar pressure distribution, foot posture, balance, ankle range of motion, and overall foot function. Participants will be randomly assigned to one of two groups: one group will perform biofeedback-assisted short foot exercises, while the other group will do traditional short foot exercises without biofeedback. Both groups will participate in supervised exercise sessions twice a week for six weeks. The study uses a randomized design with single masking to compare the two exercise approaches. During the study, participants will undergo assessments before and after the six-week exercise program. These evaluations include plantar pressure analysis, balance tests such as the Y-Balance Test, foot posture measurements like the Foot Posture Index-6, ankle range of motion tests, and self-reported questionnaires on foot and ankle ability. Researchers will monitor improvements in function and biomechanics to determine which exercise method offers greater benefits.

CONDITIONS

Brief Title

Biofeedback-Assisted Short Foot Exercises in Flexible Flatfoot

Who Can Participate

Age: 18Years - 45Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Voluntary participants aged 18 to 45 years
  • Diagnosis of flexible pes planus
  • No history of surgery, fracture, or psychiatric disorder
Not Eligible

You will not qualify if you...

  • Diagnosis of rigid pes planus
  • Age younger than 18 years or older than 45 years
  • History of psychiatric disorder or lower extremity trauma

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 weeks

Participants perform either biofeedback-assisted short foot exercises or supervised short foot exercises to improve flexible flatfoot.

1 baseline visit and 1 follow-up visit

Trial Site Locations

Total: 2 locations

1

İstanbul University-Cerrahpaşa

Istanbul, Büyükçekmece, Turkey (Türkiye), 34500

Not Yet Recruiting

2

Department of Orthopedics and Traumatology, Istanbul Faculty of Medicine, Istanbul University

Istanbul, Fatih, Turkey (Türkiye), 34104

Actively Recruiting

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Research Team

T

Taner Alparslan, Physiotherapist

S

Sezen KARABÖRKLÜ ARGUT, Asst. Prof. Dr.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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