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Can posture predict how well you move? a new analysis investigates

NCT ID NCT07786415

Knowledge-focused Sponsor: Al-Zaytoonah University of Jordan Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 26, 2026 · Last updated Aug 27, 2026 · Updated 1 time

Summary

This study looks at whether spinal alignment can predict functional performance in people with upper cross syndrome, a postural condition. It re-analyzes data from a previous trial where participants did breathing exercises and manual therapy. Researchers will measure spinal curvature with a device and test walking and mobility. The goal is to see if posture plays a key role in recovery.

What this could mean

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

Active substance
Ujjayi pranayama (breathing exercise) combined with osteopathic manipulative treatment
What this could lead to
If spinal alignment predicts functional outcomes, it could guide more targeted rehabilitation for upper cross syndrome, improving posture and mobility.
What could go wrong
This is a secondary analysis of a small trial (40 participants), so findings may be limited and not generalizable. The relationship may be correlational, not causal.

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 40 people

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

Expected to start

Aug 2026

An estimate. Start dates often move.

Expected to finish

Oct 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

20 to 29 years

Sex

Male participants only

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: * Full time college students of age 20-29 years. * Subjects who have upper cross syndrome according to REEDCO posture assessment. * Subjects who not receiving medical treatment for respiratory diseases . * Subjects who have clean family medical history. Exclusion Criteria: * Subjects who engaged in additional exercise in two weeks, which was likely to affect the results of the research . * Individuals with a history of spine, shoulder fractures, surgery, or other disease. * Individuals with severe cardia-cerebrovascular disease. * Individuals who will have difficulty to follow-up testing). * Neurologic and psychiatric disorders (who can not understand the research project ). * Individuals with congenital deformities

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Conditions

The condition(s) this trial relates to.

oculocerebral hypopigmentation syndrome of Preus

As listed by the trial registrant

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

Functional performance Spinal alignment Upper cross syndrome

How to take part

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  1. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

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  2. A doctor treating you

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