AzTrials
AzTrials

Chronic Low Back PainVRFRNCT06724679

VRFR- Immersive Virtual Reality Use in a Spine Functional Restoration Program - A Feasibility Study

A study testing Utilisability of an immersive VR device in a functional restoration program (FRP) for patients with chronic low back pain. in people with Chronic Low Back Pain, run by University Hospital, Angers at 5 sites in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

This clinical trial investigates the feasibility of integrating immersive virtual reality (VR) technology into a functional restoration program (FRP) for patients with chronic low back pain (CLBP). Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Chronic Low Back Pain
What is being tested?
Utilisability of an immersive VR device in a functional restoration program (FRP) for patients with chronic low back pain.
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
5 sitesFrance
Study dates
19 Mar 2025to 19 Apr 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Caregiver Inclusion Criteria:

Caregivers involved in RFR programs at participating centers and likely to use the VR tool during the program.

Consent of the caregiver to participate in the study.

Patient Inclusion Criteria:

  • Aged between 18 and 65 years.
  • Diagnosed with chronic low back pain lasting more than three months, with secondary causes excluded.
  • Candidates for integration into an RFR program at one of the participating centers.
  • Affiliated with or beneficiaries of a social security scheme.
  • Provide informed consent to participate in the study

Patient Exclusion Criteria:

  • Presence of any other condition incompatible with the RFR program.
  • Recent surgery or trauma (within the last month).
  • Contraindications for using the VR device, including unstable epilepsy, facial trauma within the last three months, hearing or visual impairments, or previous experiences of pain, dizziness, or nausea triggered by VR device use.
  • Visual impairments preventing the use of the VR device.
  • Pregnancy or breastfeeding.
  • Poor comprehension of the French language.
  • Incarceration by judicial or administrative decision.
  • Undergoing compulsory psychiatric treatment.
  • Subject to legal protection measures.
  • Incapable of providing informed consent.

Trial locations and contacts

5 sites in 1 country. Contact the study team or a site near you to ask about taking part.

5 sites in 1 country

France5 sites, 5 recruiting
  • Les capucins

    Angers, 49103

    Yoann RONZI, MD, 02.41.35.24.13 ext. +33, yronzi@les-capuucins-angers.fr

    Recruiting
  • CH Cholet

    Cholet, 49325

    Myriam FINGER, MD, 02 41 49 64 66 ext. +33, myriam.finger@ch-cholet.fr

    Recruiting
  • CH Laval

    Laval, 53015

    Romain CHAMPAGNE, MD, 02 43 66 50 00 ext. +33, champagne.rom@gmail.com

    Recruiting
  • CHU Rennes

    Rennes, 35033

    Philippe CARSON-JOUZEL, MD, 02 99 28 42 18 ext. +33, Philippe.CARSON.JOUZEL@chu-rennes.fr

    Recruiting
  • Centre Hospitalier Bretagne Atlantique - Site de vannes

    Vannes, 56017

    Thomas WACQUEZ, MD, 02 97 01 41 14 ext. +33, thomas.wacquez@ch-bretagne-atlantique.fr

    Recruiting

Other trials in France

About this study

This clinical trial investigates the feasibility of integrating immersive virtual reality (VR) technology into a functional restoration program (FRP) for patients with chronic low back pain (CLBP). The study aims to assess the acceptability, usability, and impact of a VR headset on both healthcare providers and patients participating in a group-based rehabilitation program. Chronic low back pain is a leading cause of functional disability worldwide and significantly impacts quality of life. Current rehabilitation strategies, including FRP, focus on improving physical functioning through multidisciplinary approaches. However, the role of emerging technologies, particularly VR, in enhancing these rehabilitation programs remains underexplored. VR has already shown promise in reducing chronic pain and improving motor abilities, but its application in a group rehabilitation context for CLBP is novel. The study will recruit healthcare providers and patients from several centers that are part of the Lombaction network. Participants will use a VR headset designed specifically to improve motor skills and reduce pain. The primary objective is to evaluate the acceptability of the VR device by healthcare providers and patients, as well as the usability and adherence to the VR program. Secondary objectives include assessing the impact of VR on kinesiophobia, pain, functional abilities, and motor imagery capabilities. This pilot study will provide valuable insights into the feasibility of incorporating VR into group-based rehabilitation programs, offering a foundation for larger comparative trials aimed at evaluating the long-term effectiveness of VR in improving rehabilitation outcomes for chronic low back pain.

Read the detailed description

Study Overview: This multicentric, prospective, exploratory, interventional pilot study aims to assess the feasibility of integrating an immersive virtual reality (VR) headset into a functional restoration program (FRP) for patients with chronic low back pain (CLBP). Chronic low back pain is a leading cause of disability, and although current FRP approaches have demonstrated benefits, there is limited research on the integration of emerging technologies like VR into these rehabilitation programs. The primary focus of this study is to evaluate the acceptability and usability of VR technology among both healthcare providers and patients involved in group-based FRP rehabilitation. Secondary objectives include assessing the potential effects of VR on reducing kinesiophobia, improving motor imagery abilities, reducing pain, and enhancing overall functional capabilities. Study Objectives: Primary Objective: To assess the acceptability of the immersive VR headset for healthcare providers managing patients with CLBP in the context of a group-based FRP. Secondary Objectives: - To evaluate the usability and adherence of patients to the VR program.- To measure the effects of the VR sessions on kinesiophobia, motor imagery abilities, pain levels, and functional capacities. - To explore the factors influencing healthcare providers' and patients' acceptance of the VR device in this rehabilitation setting. Study Design: This study is designed as a pilot, multicentric, prospective, and interventional trial. Participants will be recruited from healthcare centers within the Lombaction network, a research-driven initiative for the management and evaluation of CLBP. Patients will receive standard FRP rehabilitation, along with 3 weekly VR sessions designed to enhance motor function and reduce pain through specific exercises targeting the spine and trunk. The VR system used is an immersive, wireless headset, designed to allow a wide variety of movement and requires no external controllers. Intervention: Patients will receive the standard FRP rehabilitation, which includes a combination of physiotherapy, hydrotherapy, occupational therapy, adapted physical activity, and therapeutic education workshops. The VR intervention will involve the use of a headset with pre-programmed exergames designed to improve trunk movement (flexion, extension, rotation, etc.). Each session will last 20 minutes, with exercises lasting 5-7 minutes each, aligned with current best practices in rehabilitation. The VR device is designed to be intuitive, requiring minimal setup, and will be used in a dedicated space at the rehabilitation center. In addition to the regular rehabilitation program, participants will engage in VR sessions three times per week for the duration of the FRP, which lasts 4-5 weeks. The VR sessions are intended to complement and enhance the physical rehabilitation by promoting movement, addressing kinesiophobia, and providing immersive, distraction-based pain management. Data Collection: Data will be collected at several points throughout the study: Baseline: At the beginning of the FRP, all patients will complete several questionnaires, including the Dallas Pain Questionnaire (DPQ), Tampa Scale for Kinesiophobia (TSK), Low Back Imagery Questionnaire, and a Visual Analog Scale (VAS) to assess pain. During the program: Patients will complete VAS assessments before and after each VR session. Weekly adherence data will be collected, noting whether the VR session was completed and the reasons for any missed sessions. End of the program: At the end of the FRP, participants will complete the same questionnaires as at baseline, as well as an additional acceptability questionnaire, and the System Usability Scale (SUS) to assess the usability of the VR device. Conclusion. This pilot study is designed to explore the feasibility of incorporating immersive VR technology into an existing FRP for patients with chronic low back pain. The results will provide valuable insights into the acceptability, usability, and potential therapeutic effects of VR in a group rehabilitation setting. If successful, this study could pave the way for larger trials to evaluate the long-term benefits of VR in the management of chronic low back pain and its integration into multidisciplinary rehabilitation programs.

Being tested
Utilisability of an immersive VR device in a functional restoration program (FRP) for patients with chronic low back pain.
Keywords
Functionnal Restauration Program, Chronic low Back Pain, Immersive Virtual Reality

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Utilisability of an immersive VR device in a functional restoration program (FRP) for patients with chronic low back pain.Other

    Patients participating will engage in three 20-minute VR sessions per week, in addition to the standard FRP program, for a duration of four to five weeks. The sessions will consist of a series of pre-programmed exercises designed to facilitate various trunk movements (flexion, extension, inclination, rotation) through exergames. Each exercise will last an average of 5 to 7 minutes. These exercises have been developed in collaboration between the company providing the VR device and the rehabilitation teams. Patients will be set up by a healthcare provider in a dedicated room for VR use. The provider will configure the device, assist the patient in donning it, and initiate the program, will remain present throughout the session to monitor for any adverse effect

    . While the specific exercises may vary, the total duration of the session will be 20 minutes, consisting of various exercises interspersed with breaks. The principal investigator will propose a standardized series of exercises,

Study groups in NCT06724679
Study groupRoleWhat they receive
ExperimentalExperimentalNot described
Receives: Other: Utilisability of an immersive VR device in a functional restoration program (FRP) for patients with chronic low back pain.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Acceptance of the VR system

    a questionnaire based on the UTAUT 2 model

    Measured: 5 weeks (last day of Functional restoration program)

Secondary outcomes (3)
  1. Usability

    System Usability Scale

    Measured: 5 weeks (last day of Functional restoration program)

  2. Functional disability

    Dallas Pain Questionnaire (DPQ)

    Measured: day 1 and day 35 (First and Last day of the functional restauration program)

  3. Patient pain

    Visual Analog Scale

    Measured: day 1 and day 35 (First and Last day of the functional restauration program) and during VR session (before and after session)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Dec 2024
  2. Study start19 Mar 2025
  3. Primary completion19 Mar 2026 (estimated)
  4. Study completion19 Apr 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Model description
This study is a multicentric, prospective, exploratory interventional pilot trial aimed at assessing the feasibility of using an immersive VR device in a functional restoration program (FRP) for patients with chronic low back pain.
Masking
None (open label)
Enrolment
20 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06724679
Sponsor's protocol ID
49RC24_0176
Other IDs
2024-A01741-46
Acronym
VRFR
Status last verified
Jun 2025
First submitted
29 Nov 2024
Last updated
17 Jun 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Champagne R, Ali P, Ronzi Y, Dinomais M. Study protocol: use of virtual reality in a functional restoration programme for the spine-single-arm acceptance study. BMJ Open. 2025 Nov 26;15(11):e106366. doi: 10.1136/bmjopen-2025-106366.

    PubMed 41298262

Questions about this trial

What is this clinical trial studying?

A study testing Utilisability of an immersive VR device in a functional restoration program (FRP) for patients with chronic low back pain. in people with Chronic Low Back Pain, run by University Hospital, Angers at 5 sites in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 17 Jun 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 5 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Romain CHAMPAGNE, MD (2 43 66 55 68 ext. +33, champagne.rom@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Acceptance of the VR system (time frame: 5 weeks (last day of Functional restoration program)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06724679, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Jun 2025.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in