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New study tests taping technique for scoliosis pain relief

NCT ID NCT07428083

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 whether adding Kinesio Taping to Schroth therapy helps reduce back pain and improve daily function in young adults (ages 18-30) with mild idiopathic scoliosis. Participants will be split into three groups: one gets Schroth therapy plus real Kinesio Taping, one gets Schroth therapy alone, and one gets Schroth therapy with a sham (fake) tape. The treatment lasts 4 weeks, and pain and disability are measured at several points. The goal is to see if the tape provides extra benefit beyond exercise alone.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 51 people

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

Expected to start

Feb 2026

An estimate. Start dates often move.

Expected to finish

Nov 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.

Ages

18 to 30 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: * Individuals aged between 18 and 30 years. * Radiologically confirmed diagnosis of idiopathic scoliosis. * Cobb angle between 10° and 30° and considered candidates for conservative treatment. * Risser stage 5. * History of low back or back pain within the last 3 months (defined as NRS ≥ 4). * No acute orthopedic or neurological condition that would prevent participation in physical exercise interventions. * Willingness to participate voluntarily and provide written informed consent. * Ability to attend treatment sessions regularly throughout the study period. Exclusion Criteria: * Diagnosis of non-structural (functional) scoliosis, congenital scoliosis, or neuromuscular scoliosis. * History of previous spinal surgery. * Participation in scoliosis-specific exercise therapy within the last 6 months. * Presence of open wounds, dermatological conditions, or allergy to taping materials. * History of psychiatric disorders or neurological diseases.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

How to take part

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

  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

    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.

Contacts and locations

Locations

  • Fatih Sultan Mehmet Training and Research Hospital

    Istanbul, Istanbul, 34752, Turkey (Türkiye)

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