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Mind over matter: study probes pain beliefs in Leg-Lengthening recovery

NCT ID NCT07438821

Knowledge-focused Sponsor: Istanbul Aydın University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at how people's beliefs about pain influence their actual pain and physical function after cosmetic leg-lengthening surgery. Researchers will measure pain intensity, pain-related thoughts, and walking ability in 17 healthy men four weeks after surgery. The goal is to improve rehabilitation plans by understanding the connection between mindset and recovery.

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 58 people

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

Expected to start

Mar 2026

An estimate. Start dates often move.

Expected to finish

Jul 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

The study population consists of adults aged 20 to 50 years who underwent bilateral lower extremity cosmetic lengthening surgery using the LON (Lengthening Over Nail) technique and are attending routine postoperative follow-up at week 4 in a single tertiary care center.

Ages

20 to 50 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * Age between 20 and 50 years * Underwent bilateral lower extremity cosmetic lengthening surgery using the LON (Lengthening Over Nail) technique * Completed postoperative rehabilitation process * Attending routine clinical follow-up at postoperative week 4 * Able to understand and complete questionnaires * Provided written informed consent Exclusion Criteria: * History of orthopedic surgery other than lower extremity lengthening * Presence of neurological, rheumatologic, or systemic diseases affecting physical performance * Postoperative complications such as infection, pseudoarthrosis, or implant failure * Any condition preventing participation in physical assessment * Incomplete clinical records

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Conditions

The condition(s) this trial relates to.

Pain, Postoperative

As listed by the trial registrant

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

Limb lengthening Postoperative pain after limb lengthening

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. 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 ↗

  2. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.