Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

VR physiotherapy: a new hope for back pain sufferers?

NCT ID NCT07463105

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 compares virtual reality-based rehabilitation to standard physiotherapy for people with chronic low back pain. Eighty participants aged 40-65 will be split into two groups: one doing VR exercises plus standard care, the other only standard care. The goal is to see if VR can improve pain, balance, mobility, and quality of life over four weeks, with follow-up at eight weeks.

What this could mean

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

Active substance
Virtual reality-assisted rehabilitation (non-immersive VR training using Tecnobody Homing Studio system)
What this could lead to
If successful, this could offer a more engaging and effective rehabilitation option for chronic low back pain, potentially improving pain, mobility, and quality of life.
What could go wrong
This is a small, early-stage trial with only 80 participants, so results may not apply to everyone. The VR approach may not be significantly better than standard physiotherapy, and long-term benefits are unknown.

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 80 people

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

Expected to start

Apr 2026

An estimate. Start dates often move.

Expected to finish

May 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

40 to 65 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: * Diagnosis of chronic low back pain lasting at least 3 months * Average pain intensity ≥4/10 during the previous week on the Numeric Rating Scale (NRS) * Age between 40 and 65 years * Ability to walk independently without assistive devices * Functional disability related to low back pain defined as Oswestry Disability Index (ODI) ≥15% * No contraindications to participation in a physiotherapy program or virtual reality training * Ability to understand study procedures and follow instructions * Written informed consent to participate in the study Exclusion Criteria: * Acute low back pain or pain lasting less than 3 months * Neurological, orthopedic, rheumatological, oncological diseases or active inflammatory conditions that may affect study outcomes * Cognitive impairment limiting the ability to understand instructions or participate in rehabilitation * Contraindications to virtual reality training such as severe dizziness, nausea, epilepsy, or severe visual or auditory impairment * Contraindications to body composition analysis (e.g., implanted cardiac pacemaker or other electronic implants) * Unstable medical condition or uncontrolled cardiovascular or respiratory disorders preventing participation in rehabilitation * Participation in other rehabilitation programs during the study period * Failure to complete the four-week rehabilitation program * Lack of written informed consent

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Chronic low back pain are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

Kinesiophobia

As listed by the trial registrant

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

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

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

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Sensoreh Pastyrzak Centrum rehabilitacji niemowląt, dzieci i dorosłych

    RECRUITING

    Sanok, Podkarpackie Voivodeship, 38-500, Poland

More trials for these conditions

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