Chronic PainVRalgiaNCT06611566
VR-guided Exercise and Mindfulness Program for People with Chronic Pain
A study testing VR-guided aerobic exercise, VR-guided mindfulness exercise and TV-guided aerobic exercises in people with Chronic Pain and Rehabilitation, run by Inland Norway University of Applied Sciences at 2 sites in Norway.
Trial summary
In this study we assessed the feasibility of a VR-guided intervention seeking to improve physical fitness in individuals with chronic pain. In a randomised controlled trial with a cross-over design and participants in rehabilitation for chronic pain were asked to perform, in a counter-balanced order, five minutes of… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Chronic Pain, Rehabilitation
- What is being tested?
- VR-guided aerobic exercise, VR-guided mindfulness exercise and TV-guided aerobic exercises
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 27 participants
- Where
- 2 sitesNorway
- Study dates
- 1 Aug 2022to 1 Mar 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
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 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- The inclusion criteria were adults (\>18 years of age) with chronic musculo-skeletal pain.
Who cannot join
- The exclusion criteria were inability to perform VR-delivered physical exercise
Trial locations and contacts
2 sites in 1 country.
Norway2 sites
Inland Norway University of Applied Sciences
Elverum, Norway, 2406
Stiftelsen Hernes Institutt
Hernes, Norway, 2410
About this study
Official title: Virtual-reality-guided Exercise and Mindfulness Program for People with Chronic Pain Under Rehabilitation: a Randomised Controlled Cross-over Trial
In this study we assessed the feasibility of a VR-guided intervention seeking to improve physical fitness in individuals with chronic pain. In a randomised controlled trial with a cross-over design and participants in rehabilitation for chronic pain were asked to perform, in a counter-balanced order, five minutes of aerobic exercise following identical instructions given through either a VR headset or TV screen. The procedures were then repeated with mindfulness exercises. Heart rate (HR) was monitored throughout all four sessions and participants self-reported perceived exercise intensity, benefit, relaxation, and reward. Paired Student's t-test, Wilcoxon signed rank test and McNemar's test were performed to compare the outcome variables across sessions for individuals, as appropriate.
Read the detailed description
Participants: were recruited through partner patients' organizations, a local exercise group aimed at people living with rheumatological conditions, and an inpatient occupations rehabilitation centre.
The study was conducted according to the Helsinki declaration and approved by the Local committee for medical and health research ethics at the Inland Norway University of Applied Sciences (Ref. 20616405).
Study design The study was designed as a randomised controlled trial with a cross-over design.
Intervntion: Each participant underwent five exercise sessions in total. Firstly, all participants performed a six- minutes warm-up session following instructions projected on a TV screen. Subsequently, the participants performed two aerobic exercise sessions, identical in content and duration (five- minutes), once following the instructions from VR (VR-A) and once following the identical program that was displayed on a TV screen (TV-A). The allocation of the first aerobic exercise session as VR-A or TV-A was randomly assigned for each individual. After completing the first aerobic exercise session, the participants were subsequently asked to complete the second session guided through the opposite mode of delivery. After the exercise sessions the same randomised cross-over design was followed for two five- minute mindfulness sessions, with the participants undergoing, in a counter-balanced and random order, a guided mindfulness program, once delivered through VR (VR-M) and once displayed on a TV screen (TV-M).
Virtual environment and technology In the VR-A and VR-M, the participants wore a stand-alone HMD (Oculus Quest 2 with stock headstrap, Meta Platforms, Menlo Park, California, USA). The virtual environment was developed by Fynd Reality AS (Hamar, Norway), in line with general criteria outlined during the participatory process and consisted of a computer-generated replication of Hamar's town square (Norway). Each participant would enter this town square as a virtual avatar with virtual arms and body. The position of the arms was tracked by the hand-held controllers. A large screen would appear in the virtual town square, showing a video in which an instructor guided the exercises for the various sessions. This was the same video as shown on the TV screen.
Data collection at baseline Participant were assessed according to the Polysymptomatic Distress Scale (PDS). The Widespread Pain Index and Symptom Scale that together compose thePDS were completed by participants. The PDS is composed of variables used in the 2010 American College of Rheumatology (ACR) fibromyalgia criteria which were later modified for use in clinical research and self-evaluation in epidemiological surveys 17-19. The PSD is thus both a diagnostic aid and a measure of fibromyalgia severity. A diagnosis of fibromyalgia may be indicated by a PSD score of 12 or more in an epidemiological study1. The PDS has been translated and validated in Norwegian 20.
Outcome measures HR was registered throughout the sessions using a HR-monitors worn at the wrist (Garmin® Forerunner 55). The mean HRs for the last three minutes of each session were calculated for each individual. For the aerobic exercise sessions, HR was also categorised into HR-zones according to the ACSM recommendations based on the participants' predicted maximal HR (220 minus age) 4, with the proportion of time spent in " moderate-vigorous exercise intensity" (HR 65% of maximum heart rate or more) being calculated and used for further analysis.
Participants also completed questionnaires
Statistics We compared the mean HR values recorded within the last three minutes of the warm-up vs. all other sessions, as well between each aerobic exercise (VR-A vs. TV-A) and mindfulness sessions (VR-M vs. TV-M), using paired Student's t-test.
The time spent in each HR category was compared using the paired Wilcoxon signed rank test and time in the "moderate-vigorous" vs "low" ACSM zone in the VR-A vs. TV-A sessions using McNemar's test for dichotomised variables.
Comparisons between the self-reported measurements collected after the aerobic exercise (VR-A vs. TV-A) and mindfulness sessions (VR-M vs. TV-M) were performed using the paired Wilcoxon signed rank test for each session for ordinal data and McNemars test for dichotomised variables.
- Conditions
- Chronic Pain, Rehabilitation
- Being tested
- VR-guided aerobic exercise, VR-guided mindfulness exercise, TV-guided aerobic exercises, TV-guided mindfulness exercises
- Keywords
- adult, humans, rehabilitation, virtual reality, chronic pain
- Medical subject headings
- Chronic Pain
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
VR-guided aerobic exerciseBehavioural
The intervention was 5 minutes of VR-guided aerobic exercise
VR-guided mindfulness exerciseBehavioural
The intervention was 5 minutes of VR-guided mindfulness exercise
TV-guided aerobic exercisesBehavioural
The intervention was 5 minutes of TV-guided aerobic exercises
TV-guided mindfulness exercisesBehavioural
The intervention was 5 minutes of VR-guided mindfulness exercises
| Study group | Role | What they receive |
|---|---|---|
| VR-guided aerobic exercise then TV-guided aerobic exercise | Experimental | Participants were randomised to VR-guided aerobic exercise followed by TV-guided aerobic exercise Receives: Behavioral: VR-guided aerobic exercise; Behavioral: TV-guided aerobic exercises |
| TV-guided exercise then VR-guided aerobic exercise | Experimental | Participants were randomised toTV-guided aerobic exercise followed by VR- aerobic guided exercise Receives: Behavioral: VR-guided aerobic exercise; Behavioral: TV-guided aerobic exercises |
| VR-guided mindfulness exercise then TV-guided mindfulness exercise | Experimental | 5 minutes of VR-guided mindfulness exercise followed by 5 minutes of TV-guided mindfulness exercise Receives: Behavioral: VR-guided mindfulness exercise; Behavioral: TV-guided mindfulness exercises |
| TV-guided mindfulness exercise then VR-guided mindfulness exercise | Experimental | 5 minutes of TV-guided mindfulness exercise followed by 5 minutes of VR-guided mindfulness exercise Receives: Behavioral: VR-guided mindfulness exercise; Behavioral: TV-guided mindfulness exercises |
What is being measured
The primary outcome is the main question the study is designed to answer.
Heart rate
HR was registered throughout the sessions using a HR-monitors worn at the wrist (Garmin® Forerunner 55). The mean HRs for the last three minutes of each session were calculated for each individual. For the aerobic exercise sessions, HR was also categorised into HR-zones according to the ACSM recommendations based on the participants' predicted maximal HR (220 minus age) 4, with the proportion of time spent in " moderate-vigorous exercise intensity" (i.e., HR \> 65% of maximum heart rate) being calculated and used for further analysis.
Measured: For duration of interventions, an average of 30 minutes.
Secondary outcomes (4)
Exercise intensity
Participants self-reported exercise intensity after each aerobic sessions by completing a short paper questionnaire. The question was phrased as follow: "How challenging was the session" rated on a 5-point Likert scale ranging from 1 (least imaginable) to 5 (most imaginable).
Measured: After 10 minutes
Perceived degree of relaxation
After each mindfulness sessions, the participants were asked to complete a short questionnaire regarding the degree of relaxation. The question was phrased as follow: "How relaxing was the session?" rated on a 5-point Likert scale ranging from 1 (least imaginable) to 5 (most imaginable).
Measured: After 10 minutes
Perceived reward
After each mindfulness sessions, the participants were asked to complete a short questionnaire regarding the degree of perceived reward. The question was phrased as follow:"How rewarding was the session?" rated on a 5-point Likert scale ranging from 1 (least imaginable) to 5 (most imaginable).
Measured: After 10 minutes
Exercise adherence
Participants self-reported personal adherence directly after each aerobic sessions by completing a short paper questionnaire. The question was phrased as follow: "How well did you exercise?" rated on a 5-point Likert scale ranging from 1 (least imaginable) to 5 (most imaginable).
Measured: After 10 minutes
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Sep 2024
- Study start1 Aug 2022
- Primary completion1 Mar 2023
- Study completion1 Mar 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Chronic PainStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Randomised
- Intervention model
- Crossover
- Model description
- The studydesign was crossover and sequential. All participants tried VR- and TV- guided aerobic exercise and VR-and TV-guided mindfulness exercises, but in counterbalanced order
- Masking
- None (open label)
- Enrolment
- 27 participants (actual)
Sponsor and investigators
- Lead sponsor
- Inland Norway University of Applied Sciences
- Sponsor type
- University, hospital or other
- Collaborators
- The Research Council of Norway
- Responsible party
- Sponsor
- Investigators
- Sella A Provan, MD PHD, Study director, Inland Norway University of Applied Sciences
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06611566
- Sponsor's protocol ID
- InlandNUAS
- Acronym
- VRalgia
- Status last verified
- Sep 2024
- First submitted
- 9 Sep 2024
- Last updated
- 25 Sep 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: We have not described sharing data from this small trial in the application to the ethical committe. If a relevant party was to ask for individual level data we would consider the application and consult the ethical committee.
Publications
Provan SA, Calogiuri G, Roset L, Mariussen M, Rosoy I, Johnsen TJ, Johansen T, Flaten OE, Litleskare S. VR-guided exercise and mindfulness program for people with chronic pain: a randomised controlled cross-over pilot trial. BMC Sports Sci Med Rehabil. 2025 Mar 21;17(1):55. doi: 10.1186/s13102-025-01102-9.
PubMed 40119474
Study at a glance
From the registry record, last updated by the sponsor on 25 Sep 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Virtual-reality-guided Exercise and Mindfulness Program for People with Chronic Pain Under Rehabilitation: a Randomised Controlled Cross-over Trial
- ClinicalTrials.gov ID
- NCT06611566
- Acronym / sponsor ID
- VRalgia / InlandNUAS
- Conditions
- Chronic Pain, Rehabilitation
- Keywords
- adult, humans, rehabilitation, virtual reality, chronic pain
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 27 participants (actual)
- Lead sponsor
- Inland Norway University of Applied SciencesUniversity, hospital or other
- Collaborators
- The Research Council of Norway
- Study start
- 1 Aug 2022 (actual)
- Primary completion
- 1 Mar 2023 (actual)
- Study completion
- 1 Mar 2023 (actual)
- First posted
- 25 Sep 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
In this study we assessed the feasibility of a VR-guided intervention seeking to improve physical fitness in individuals with chronic pain. In a randomised controlled trial with a cross-over design and participants in rehabilitation for chronic pain were asked to perform, in a counter-balanced order, five minutes of aerobic exercise following identical instructions given through either a VR headset or TV screen. The procedures were then repeated with mindfulness exercises. Heart rate (HR) was monitored throughout all four sessions and participants self-reported perceived exercise intensity, benefit, relaxation, and reward. Paired Student's t-test, Wilcoxon signed rank test and McNemar's test were performed to compare the outcome variables across sessions for individuals, as appropriate.
Detailed description
Participants: were recruited through partner patients' organizations, a local exercise group aimed at people living with rheumatological conditions, and an inpatient occupations rehabilitation centre.
The study was conducted according to the Helsinki declaration and approved by the Local committee for medical and health research ethics at the Inland Norway University of Applied Sciences (Ref. 20616405).
Study design The study was designed as a randomised controlled trial with a cross-over design.
Intervntion: Each participant underwent five exercise sessions in total. Firstly, all participants performed a six- minutes warm-up session following instructions projected on a TV screen. Subsequently, the participants performed two aerobic exercise sessions, identical in content and duration (five- minutes), once following the instructions from VR (VR-A) and once following the identical program that was displayed on a TV screen (TV-A). The allocation of the first aerobic exercise session as VR-A or TV-A was randomly assigned for each individual. After completing the first aerobic exercise session, the participants were subsequently asked to complete the second session guided through the opposite mode of delivery. After the exercise sessions the same randomised cross-over design was followed for two five- minute mindfulness sessions, with the participants undergoing, in a counter-balanced and random order, a guided mindfulness program, once delivered through VR (VR-M) and once displayed on a TV screen (TV-M).
Virtual environment and technology In the VR-A and VR-M, the participants wore a stand-alone HMD (Oculus Quest 2 with stock headstrap, Meta Platforms, Menlo Park, California, USA). The virtual environment was developed by Fynd Reality AS (Hamar, Norway), in line with general criteria outlined during the participatory process and consisted of a computer-generated replication of Hamar's town square (Norway). Each participant would enter this town square as a virtual avatar with virtual arms and body. The position of the arms was tracked by the hand-held controllers. A large screen would appear in the virtual town square, showing a video in which an instructor guided the exercises for the various sessions. This was the same video as shown on the TV screen.
Data collection at baseline Participant were assessed according to the Polysymptomatic Distress Scale (PDS). The Widespread Pain Index and Symptom Scale that together compose thePDS were completed by participants. The PDS is composed of variables used in the 2010 American College of Rheumatology (ACR) fibromyalgia criteria which were later modified for use in clinical research and self-evaluation in epidemiological surveys 17-19. The PSD is thus both a diagnostic aid and a measure of fibromyalgia severity. A diagnosis of fibromyalgia may be indicated by a PSD score of 12 or more in an epidemiological study1. The PDS has been translated and validated in Norwegian 20.
Outcome measures HR was registered throughout the sessions using a HR-monitors worn at the wrist (Garmin® Forerunner 55). The mean HRs for the last three minutes of each session were calculated for each individual. For the aerobic exercise sessions, HR was also categorised into HR-zones according to the ACSM recommendations based on the participants' predicted maximal HR (220 minus age) 4, with the proportion of time spent in " moderate-vigorous exercise intensity" (HR 65% of maximum heart rate or more) being calculated and used for further analysis.
Participants also completed questionnaires
Statistics We compared the mean HR values recorded within the last three minutes of the warm-up vs. all other sessions, as well between each aerobic exercise (VR-A vs. TV-A) and mindfulness sessions (VR-M vs. TV-M), using paired Student's t-test.
The time spent in each HR category was compared using the paired Wilcoxon signed rank test and time in the "moderate-vigorous" vs "low" ACSM zone in the VR-A vs. TV-A sessions using McNemar's test for dichotomised variables.
Comparisons between the self-reported measurements collected after the aerobic exercise (VR-A vs. TV-A) and mindfulness sessions (VR-M vs. TV-M) were performed using the paired Wilcoxon signed rank test for each session for ordinal data and McNemars test for dichotomised variables.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Number of arms
- 4
- Model description
- The studydesign was crossover and sequential. All participants tried VR- and TV- guided aerobic exercise and VR-and TV-guided mindfulness exercises, but in counterbalanced order
| Arm | Type | Receives |
|---|---|---|
| VR-guided aerobic exercise then TV-guided aerobic exercise | Experimental | Behavioral: VR-guided aerobic exercise, Behavioral: TV-guided aerobic exercisesParticipants were randomised to VR-guided aerobic exercise followed by TV-guided aerobic exercise |
| TV-guided exercise then VR-guided aerobic exercise | Experimental | Behavioral: VR-guided aerobic exercise, Behavioral: TV-guided aerobic exercisesParticipants were randomised toTV-guided aerobic exercise followed by VR- aerobic guided exercise |
| VR-guided mindfulness exercise then TV-guided mindfulness exercise | Experimental | Behavioral: VR-guided mindfulness exercise, Behavioral: TV-guided mindfulness exercises5 minutes of VR-guided mindfulness exercise followed by 5 minutes of TV-guided mindfulness exercise |
| TV-guided mindfulness exercise then VR-guided mindfulness exercise | Experimental | Behavioral: VR-guided mindfulness exercise, Behavioral: TV-guided mindfulness exercises5 minutes of TV-guided mindfulness exercise followed by 5 minutes of VR-guided mindfulness exercise |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- The inclusion criteria were adults (\>18 years of age) with chronic musculo-skeletal pain.
Key exclusion criteria (1 listed)
- The exclusion criteria were inability to perform VR-delivered physical exercise
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| VR-guided aerobic exerciseThe intervention was 5 minutes of VR-guided aerobic exercise | Behavioural | TV-guided exercise then VR-guided aerobic exercise, VR-guided aerobic exercise then TV-guided aerobic exercise |
| VR-guided mindfulness exerciseThe intervention was 5 minutes of VR-guided mindfulness exercise | Behavioural | TV-guided mindfulness exercise then VR-guided mindfulness exercise, VR-guided mindfulness exercise then TV-guided mindfulness exercise |
| TV-guided aerobic exercisesThe intervention was 5 minutes of TV-guided aerobic exercises | Behavioural | TV-guided exercise then VR-guided aerobic exercise, VR-guided aerobic exercise then TV-guided aerobic exercise |
| TV-guided mindfulness exercisesThe intervention was 5 minutes of VR-guided mindfulness exercises | Behavioural | TV-guided mindfulness exercise then VR-guided mindfulness exercise, VR-guided mindfulness exercise then TV-guided mindfulness exercise |
Primary outcome
Heart rate
Time frame: For duration of interventions, an average of 30 minutes.
HR was registered throughout the sessions using a HR-monitors worn at the wrist (Garmin® Forerunner 55). The mean HRs for the last three minutes of each session were calculated for each individual. For the aerobic exercise sessions, HR was also categorised into HR-zones according to the ACSM recommendations based on the participants' predicted maximal HR (220 minus age) 4, with the proportion of time spent in " moderate-vigorous exercise intensity" (i.e., HR \> 65% of maximum heart rate) being calculated and used for further analysis.
4 secondary outcomes
Exercise intensity
Time frame: After 10 minutes
Perceived degree of relaxation
Time frame: After 10 minutes
Perceived reward
Time frame: After 10 minutes
Exercise adherence
Time frame: After 10 minutes
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Sep 2024.
- Derived from this study: PubMed 40119474Provan SA, Calogiuri G, Roset L, Mariussen M, Rosoy I, Johnsen TJ, Johansen T, Flaten OE, Litleskare S. VR-guided exercise and mindfulness program for people with chronic pain: a randomised controlled cross-over pilot trial. BMC Sports Sci Med Rehabil. 2025 Mar 21;17(1):55. doi: 10.1186/s13102-025-01102-9.
- Individual participant dataSharing planned: No. We have not described sharing data from this small trial in the application to the ethical committe. If a relevant party was to ask for individual level data we would consider the application and consult the ethical committee.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Sella A Provan, MD PHD study director
Inland Norway University of Applied Sciences
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing VR-guided aerobic exercise, VR-guided mindfulness exercise and TV-guided aerobic exercises in people with Chronic Pain and Rehabilitation, run by Inland Norway University of Applied Sciences at 2 sites in Norway.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. 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: finished, as of the sponsor's last update on 25 Sep 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Norway. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Heart rate (time frame: For duration of interventions, an average of 30 minutes.). 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 NCT06611566, 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 25 Sep 2024.