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Gentle diaphragm stretch may boost scoliosis therapy in teens

NCT ID NCT07482748

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 whether adding a simple manual diaphragm release to standard Schroth exercises can improve breathing, posture, and quality of life in adolescents with idiopathic scoliosis. Forty-two teens aged 10–18 will be randomly assigned to either Schroth exercises alone or Schroth plus diaphragm mobilization, three times a week for six weeks. Researchers will measure lung function, trunk rotation, and chest mobility at the start, end, and at a 12-week follow-up.

What this could mean

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

Active substance
Diaphragm mobilization (manual therapy technique)
What this could lead to
If it works, this could point toward a simple, non-drug way to improve breathing and posture in teens with scoliosis.
What could go wrong
This is a small, early-stage trial with only 42 participants. The added benefit of diaphragm mobilization may be small or not noticeable, and results may not apply to all scoliosis patients.

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 42 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

Jan 2027

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

10 to 18 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: * Adolescents aged between 10 and 18 years * Diagnosis of adolescent idiopathic scoliosis * Cobb angle ≥ 10° * Ability to participate in exercise sessions * Written informed consent from the participant and their parent or legal guardian Exclusion Criteria: * Non-idiopathic scoliosis (e.g., neuromuscular, congenital, or syndromic scoliosis) * Presence of congenital anomalies affecting the musculoskeletal system * Previous scoliosis treatment within the last 6 months * Participation in another physiotherapy or rehabilitation program during the study period * Current use of a scoliosis brace * History of spinal surgery * Presence of neurological, rheumatological, or cardiopulmonary diseases that may affect participation in the intervention * Cognitive impairment, communication disorders, or any condition that may limit the ability to follow instructions or complete assessments

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Conditions

The condition(s) this trial relates to.

adolescent idiopathic scoliosis Respiratory Aspiration

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 official record

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

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  2. A doctor treating you

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