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Do supportive shoes weaken feet? a study compares Long-Term effects

NCT ID NCT07735949

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jul 30, 2026 · Last updated Jul 31, 2026 · Updated 1 time

Summary

This study looks at how wearing supportive versus flat shoes every day for at least six months may change foot shape, pressure distribution, and balance in healthy adults. Researchers will measure foot pressure and stability in 40 participants. The goal is to better understand the long-term effects of habitual footwear on foot mechanics.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If clear differences emerge, this could guide footwear recommendations for maintaining natural foot function and balance.
What could go wrong
This is a small, observational study with only 40 participants. It cannot prove cause and effect, only highlight possible associations.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 40 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jul 2026

Expected to finish

Aug 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Healthy adults aged 18-35 years will be recruited from the Faculty of Health Sciences at Bahçeşehir University. Participants must have habitually worn either supportive footwear or flat footwear for at least 6 months, with an average daily use of at least 6 hours. Eligible individuals will be assigned to groups according to their habitual footwear type and will undergo assessments of plantar pressure distribution, foot posture, and balance performance.

Ages

18 to 35 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Adults aged 18 years and older * Diagnosis of hemophilia A or B * Scheduled to undergo primary total knee arthroplasty * Able to understand the study procedures and provide written informed consent * Willing to participate in the prehabilitation program Exclusion Criteria: * Presence of neurological disorders affecting balance or gait * Severe cognitive impairment * Other musculoskeletal conditions affecting lower extremity function * Revision total knee arthroplasty * Any medical condition that would prevent safe participation in the exercise program

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

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  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

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Contacts and locations

Locations

  • Bahcesehir university

    RECRUITING

    Istanbul, Istanbul, Turkey (Türkiye)

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