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One-Time back adjustment boosts core stability in healthy adults

NCT ID NCT07244679

Knowledge-focused Sponsor: Bahçeşehir 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
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 Results may not be published yet.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
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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested whether a single, quick chiropractic adjustment to the sacroiliac joint (the area where the spine meets the pelvis) could improve core stability in 60 healthy adults aged 18-40. Participants were randomly assigned to receive the adjustment or no treatment. Results showed short-term improvements in trunk stability and flexibility after the adjustment, suggesting it may temporarily enhance neuromuscular control.

What this could mean

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

Active substance
Sacroiliac joint manipulation (HVLA)
What this could lead to
If confirmed, this could point toward a simple technique to temporarily boost core stability and flexibility in healthy people.
What could go wrong
This was a small study in healthy individuals, so results may not apply to people with pain or conditions. The improvements were short-term and may not translate to real-world benefits.

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

60 people

The number who actually took part.

Started

Mar 2022

Finished

Jun 2022

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 40 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: * Healthy adults aged between 18 and 40 years * No history of low back or pelvic pain within the last 6 months * No previous spinal or sacroiliac joint surgery * No current neurological or musculoskeletal disorders * Able to maintain standing and sitting positions without discomfort * Voluntary participation with informed consent Exclusion Criteria: * History of chronic low back pain or sacroiliac dysfunction * Previous fractures, dislocations, or surgery in the lumbopelvic region * Neurological, vestibular, or systemic disorders affecting balance or movement * Pregnancy or suspected pregnancy * Use of pain medication, muscle relaxants, or anti-inflammatory drugs within the last 48 hours * Contraindications to manual therapy (osteoporosis, malignancy, inflammatory joint disease, acute disc herniation, cauda equina syndrome) * Refusal or inability to participate in the study protocol

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As listed by the trial registrant

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

Core stabilization Health adults

Contacts and locations

Locations

  • Ataşehir Florence Nightingale Hospital

    Istanbul, Turkey (Türkiye)

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