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Teens with scoliosis may benefit from targeted exercise combo

NCT ID NCT07319702

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
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 This study
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 Results may not be published yet.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
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Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Aug 20, 2026 · Updated 2 times

Summary

This study tested whether a combination of two exercise methods (proprioceptive neuromuscular facilitation and spiral muscle chain training) can improve posture, spinal flexibility, and back muscle endurance in teenagers aged 13 to 18 with spinal curvature issues like scoliosis or kyphosis. 189 participants were split into three groups: one did one type of exercise, another did the other type, and the third did both. They exercised three times a week for 12 weeks. The goal was to see if the combined approach works better than either exercise alone.

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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

189 people

The number who actually took part.

Started

Mar 2024

Finished

Dec 2024

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

13 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: * Aged 13 to 18 years * Newly diagnosed with no prior treatment and meeting the diagnostic criteria for spinal curvature abnormalities * Scoliosis or coronal spinal curvature abnormality determined by poor posture and angle of trunk inclination or angle of trunk rotation of 5° or greater * Anterior-posterior spinal curvature abnormality determined by poor posture or abnormal spinal side-view assessment, including kyphotic angle less than 20° or greater than 40° * No prior brace treatment * No history of spinal surgery * Able to complete proprioceptive neuromuscular facilitation therapy, spiral muscle chain training, or combined exercise training as required * Written informed consent obtained from participants and their parents or legal guardians Exclusion Criteria: * Menstruating females at the time of assessment * Metal implants * History of brace use or prior treatment for spinal curvature abnormalities * Severe scoliosis, defined as angle of trunk inclination or angle of trunk rotation greater than 13° * Congenital spinal curvature abnormality * Neuromuscular disorders * Respiratory dysfunction * Any contraindication to exercise * Any trauma within the previous 6 months * Any accompanying neurological, rheumatological, or mental health problems

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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.

Contacts and locations

Locations

  • The Affiliated High School of Nanjing Normal University

    Nanjing, Jiangsu, 210023, China

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Other studies related to the condition(s) this trial covers.