Can an AR headset help people with back pain move without fear?

NCT ID NCT07527845

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026

Summary

This study tested a new augmented reality (AR) system in 17 adults with chronic low back pain and a fear of movement. Participants wore a headset that showed a video of them bending further than they actually were, creating a visual illusion. The goal was to see if the device was safe, comfortable, and could help increase their range of motion and reduce fear.

What this could mean

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

Active substance
Augmented reality rehabilitation system (AnReal)
What this could lead to
If this approach works, it could offer a new, non-drug way to help people with chronic back pain move more freely and overcome their fear of bending.
What could go wrong
This was a very small, early feasibility study with only 17 participants. The results may not apply to everyone, and the device might cause dizziness or nausea in some users.

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.

Participants

17 people

The number who actually took part.

Started

Dec 2022

Finished

Nov 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.

Who is studied

The study population consists of two distinct groups recruited for a proof-of-concept and a feasibility trial. The first group includes healthy adult volunteers used for the initial technical validation of the system. The primary clinical group consists of adult patients suffering from non-specific chronic low back pain and kinesiophobia, specifically characterized by a significant limitation in spinal range of motion. All participants were evaluated in a controlled research environment to assess the safety and performance of the AR technology

Ages

18 years and older

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: * Participants must be over 18 years old. * For the pilot phase: Healthy volunteers with no chronic pathologies or musculoskeletal conditions * For the clinical phase: Diagnosis of non-specific chronic low back pain (CLBP) lasting longer than three months. * For the clinical phase: Presence of less than 40 degrees of spinal forward bending movement. Exclusion Criteria: * History of spine surgery. * Diagnosis of vestibular disorders. * Diagnosis of Meniere's syndrome

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Conditions

The condition(s) this trial relates to.

Kinesiophobia Low Back Pain

As listed by the trial registrant

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

Contacts and locations

Locations

  • Pontificia Universidad Católica de Chile

    Santiago, Chile

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