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Virtual RealityVR4POPKANCT03665233

Virtual Reality for Post Operative Pain Management After Total Knee Arthroplasty

A study testing VR in people with Virtual Reality and Pain, Postoperative, run by Clinique Saint-Jean, Bruxelles at 1 site in Belgium.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

Virtual reality has been used for acute pain management (burn patients) with positive results. Hypnosis has known beneficial effects on patients in the peri-operative setting. The investigators are combining both by giving a virtual reality hypnosis (VRH) session to the patients during a known painful post-operative… Read more about this study

Who is it for?
Ages 18 to 85 years
What is being tested?
VR
Type of treatment
Medical device
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
40 participants
Where
1 siteBelgium
Study dates
1 Sep 2020to 30 Nov 2020
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 to 85 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients having a TKA
  • General anesthesia and single shot fem block
  • Adults (> 18 years)
  • Elective procedures

Who cannot join

  • Refusal of consent
  • History of seizures
  • History of drug abuse
  • History of psychiatric diseases
  • Patients with impaired hearing
  • Patients with impaired vision
Show all 10Show fewer
  • Patients afraid of submarine worlds
  • Chronic pain patients
  • Claustrophobia
  • Language not available on VR system

Trial locations and contacts

1 site in 1 country.

Belgium1 site
  • Clinique Saint Jean

    Brussels, 1000

Other trials in Belgium

About this study

Official title: Virtual Reality for Post Operative Pain Management After Total Knee Arthroplasty: a Randomized, Controlled, Multi-center, Double Blind, Parallel Group, Superiority Trail to Evaluate VR as a Component of a Multi-modal Pain Treatment

Virtual reality has been used for acute pain management (burn patients) with positive results. Hypnosis has known beneficial effects on patients in the peri-operative setting. The investigators are combining both by giving a virtual reality hypnosis (VRH) session to the patients during a known painful post-operative moment. (physiotherapy) It is the investigator intention to compare pain after physiotherapy during the first 3 days after a total knee arthroplasty, between 2 groups. One group , the VR group gets standard treatment with VRH and the second, the sham group, gets standard treatment with a sham VR session.

Read the detailed description

Introduction: Postoperative pain frequently occurs after total knee arthroplasty. The IASP defines pain as "an unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described in terms of such damage". Pain is a major cause of post-operative distress and has a variety of side effects and complications. Chronic post surgical pain is probably the most feared complication of acute pain. Therefore, adequate pain control after surgery is mandatory.

In modern western healthcare, multi-modal pain treatment is the standard of care. This means that a variety of drugs, acting on different receptors, are used alongside non-pharmacological interventions, to decrease pain. Such an approach enables the physician to use a lower concentration of a specific drug, in order to avoid adverse effects that can occur when giving higher doses of one individual drug. These drugs are based on the analgesic ladder of the WHO to relief cancer pain. From the different drugs that are used, the major concern will be with the opioids, as they are known to have major complications. Especially today in the USA there is an epidemic of opioid related deaths. Very often these drugs have been prescribed in a post-operative setting. The search for a different non-pharmacological analgesic treatment is today, more than ever, a pressing need.

Virtual reality (VR) is a non-pharmacological way to decrease pain in a number of different situations. It has been around for some years, some articles describing VR in medicine are 25 years old but it only recently became a popular medical treatment since the introduction of the Oculus Rift in 2014. Before that HMDs (head-mounted display) were expensive and very bulky devices. Since the introduction of the Oculus Rift HMD the availability and usability of VR has increased dramatically.

In the post-operative period pain at rest is generally reported to be acceptable by our patients (VAS<3), but if movements are involved the pain increases to unacceptable levels. Postoperative physiotherapy generally involves the use of a continuous passive motion (CPM), a machine used for passive bending of the knee. This postoperative mobilization is one of the major causes of pain in the aftermath of a total knee arthroplasty.

Available evidence: Virtual Reality (VR) has been shown to reduce pain in different situations. From experimental pain in healthy subjects to changing dressing of burn patients, several studies have shown the use of immersive VR therapy as an adjunct for pain treatment.

The use of VR in children has frequently been studied, as it decreases pain and anxiety during painful medical procedures.

The combination of VR and standard treatment (ST) has shown to have a superior analgesic efficacy compared to VR or ST alone .

In the medical VR world there are different types of applications. Some of these act as "distractors" (playing games, looking at natural scenery) and some have included elements of therapeutic hypnosis. With these applications the patients are (self)-induced in a hypnotic state.

Medical hypnosis has been shown to have a tremendous impact on post-operative recovery, reducing anxiety and pain. Medical hypnosis is a one on one intervention, making it time and labor consuming and people using hypnosis need to be well trained to perform the technique safely. Bringing a patient in a hypnotic state can only be achieved by using appropriate verbal quotes and this can be problematic if the patient speaks another language.

Although the surgical population would benefit greatly by using medical hypnosis, only few patients are offered this technique.

Using a VR application with therapeutic hypnotic elements can be a great way to share with many patients the positive effects of hypnotic therapy.

Trial : the investigators decided therefore to use a medical VR application that includes therapeutic hypnotic elements. They want to compare the analgesic efficacy of standard treatment with medical virtual reality and standard treatment with a sham VR session in postoperative pain management, after the patient have had a session of physiotherapy, as this is a painful moment in the post operative period. Using a sham VR session is lickely to produce some sort of analgesia as any disctraction with VR can have a positive effect. But this sham session isn't an enjoyable VRH session, therefore the authors still expect a significant difference in pain reduction.

Using the sham seems inevitbale because it is not possible to blind the patients otherwise to their own traetment. If the authors would use use a control group there would be a high risk of biais because of the dissapointement for the patients not receiving any VR.

Each includable patient will be approached before the day of surgery and asked for participation in the study, after verifying the absence of any exclusion criteria.

The investigators will present the study to the patients, using a patient oriented explicatory form, after which they will look at the informed consent together with the patient. If necessary they will give the patient some time to reflect and come back after a while, to sign and collect, or not, the informed consent.

Randomization will be done earlier using a web based block randomization program : www.randomization.com Each patient will be assigned to either a standard treatment with VR sham group (Sh-group) or a standard treatment with Virtual reality group (VR-group). The virtual reality will be an application designed by Oncomfort®. It is a session called AQUA, which includes an underwater experience guided by a whale. The VR sham experience is also an underwater based experience but without any coherence between the different images. The HMD is a VR Gear from Samsung-Oculus and the mobile phone used is a Samsung Galaxy 7.

Interventions happen on the day of surgery (DOS), on post operative day 1-2 and 3 (POD1, POD2 and POD3. )

On the day of surgery :

Before going to the OR each included patient (both VR and Sh group) fills in a STAI Y questionnaire gives a VAS pain score Before going to the OR, patients in the VR group get additionally a 45 min session of VR : AQUA and patients in the Sh group get 45 min of a sham session.

Each patient gets a TKA. There is no interference with the anaesthesia protocol. This is, as usual, decided between the patient and the anaesthetist working in the OR. Some parts of the peri-operative and the post-operative protocols however are standardized:

Peroperative General anesthesia Paracetamol 1g every 6 h If there are no contra-indications : anti-inflammatory drugs (ketorolac) 3x/d IV, (including a PPI (proton pump inhibitor) if necessary) Dexamethasone 0,5 -1 mg/kg Tranexamic acid 1 g Use of a tourniquet by the surgeon Infiltration of the posterior part of the knee by the surgeon with levobupivacaine 0.2% PCIA Morphine Femoral nerve block single shot (with 15 ml levobupivacaine 0,25% ) , before the start of the surgery Postoperative Paracetamol Anti-inflammatory drugs PCIA morphine Ice application 3 times a day Rescue medication : Tramadol 50 mg, max 6 per day

POD1-POD2 -POD3 During the post operative days patients get passive mobilization of the knee with the CPM device (Kinetec).

During this exercise patients in the VR-group get a 45 minute VR session and teh Sh-group gets a 45 min sham session. The physiotherapist (who gets a specific training) or another investigator will put on the mask. The CPM device starts 10 min after the start of the VR session. All the patients get standard care, which means they can use their PCIA morphine, as required.

After each session a blinded investigator measures the VAS pain score, the anxiety score with the STAY-I questionnaire and the morphine consumed.

On POD3 or on the day of discharge (if earlier) patients will be asked to rate their satisfaction (with a VAS). The physiotherapist will also rate their appreciation of the functional rehabilitation, by comparing the increase of passive flexion between POD1 and POD3.

Total morphine consumption (until POD3) and length of stay will be recorded.

Being tested
VR
Medical subject headings
Pain, Postoperative

What participants receive

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

  • VRDevice

    Also called Aqua VRH session, Oncomfort, Gear VR

    People in the VR-group get a VRH session during the CPM physiotherapy , people in the sham group get a VR sham session, while they both can enjoy Standard Treatment

Study groups in NCT03665233
Study groupRoleWhat they receive
Sh-groupSham comparatorThe patients in this arm get standard treatment, together with a sham version of a VR session.
Receives: Device: VR
VR-groupActive comparatorThese patients get a VR session with the standard treatment
Receives: Device: VR

What is being measured

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

  1. The comparison of opioid consumption after physiotherapy, when using VRH or VR sham

    After each physiotherapy session with continuous passive movement (CPM), a blinded investigator will measure the opioid consumption .

    Measured: on post operative day 1

  2. The comparison of opioid consumption after physiotherapy, when using VRH or VR sham

    After each physiotherapy session with continuous passive movement (CPM), a blinded investigator will measure the opioid consumption

    Measured: on post operative day 2

  3. The comparison of opioid consumption after physiotherapy, when using VRH or VR sham

    After each physiotherapy session with continuous passive movement (CPM), a blinded investigator will measure the opioid consumption

    Measured: on post operative day 3

Secondary outcomes (5)
  1. The change in anxiety measured with an anxiety scale, after physiotherapy, between the control (standard treatment ) and the VR group (standard + VR treatment)

    After each physiotherapy session with CPM, a blinded investigator will measure the anxiety using STAI Y. The State Trait Anxiety Inventory. This is a questionnaire of 20 questions assessing a patients state of anxiety. The answer to every questions can be rated from 1 until 4. The high rthe score the higher the anxiety.

    Measured: on post operative day (POD) 1-2-3

  2. The variation in patient satisfaction at the end of the third day, between the participants using the VRH or not.

    after post operative day 3 a blinded investigator will measure the satisfaction score using (VAS) visual analogue scale. This is a scale going from no satisfaction at all until the best satisfaction one can imagine. The scale is like a horizontal yardstick with a cursor and the patient is asked to move to cursor to the level of his satisfaction. On the other side of the scale is a metric system from 0-10 cm. This way the satisfaction can be scored out of 10. The higher the number the better the satisfaction.

    Measured: on post operative day (POD) 3

  3. The comparison in pain after post-operative physiotherapy using VAS

    a blinded investigator will measure the VAS pain score after each physiotherapy session involving a CPM.This is a scale going from no satisfaction at all until the best satisfaction one can imagine. The scale is like a horizontal yardstick with a cursor and the patient is asked to move to cursor to the level of his satisfaction. On the other side of the scale is a metric system from 0-10 cm. This way the pain can be scored out of 10. The higher the number the worser the pain

    Measured: on post operative day 1-2-3

  4. The comparison of the evolution of the knee flexion with the CPM (Continuous passive motion) when using VRH or not

    Measure the increase of flexion of the knee on the CPM device between POD1 and POD3

    Measured: on post operative day 1 and 3

  5. The variance in the length of stay after a total knee arthroplasty between the treatment and the control group.

    measuring the length of stay at the hospital, from the day (and hour) of surgery, until the patient is ready for discharge (day and hour). This is the moment the operator decides that the patient is fit enough to leave the hospital.

    Measured: This will be assessed 1 week after surgery

Timeline

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

  1. First posted11 Sep 2018
  2. Study start1 Sep 2020
  3. Primary completion30 Nov 2020
  4. Study completion30 Nov 2020

Why it stopped: not enough patients (covcid restrictions)

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
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
40 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03665233
Sponsor's protocol ID
VRAB001
Other IDs
2018-001559-10, 2018
Acronym
VR4POPKA
Status last verified
Jul 2021
First submitted
2 Sep 2018
Last updated
23 Jul 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing VR in people with Virtual Reality and Pain, Postoperative, run by Clinique Saint-Jean, Bruxelles at 1 site in Belgium.

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 4 inclusion and 10 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: stopped early, as of the sponsor's last update on 23 Jul 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Belgium. 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. Some participants in this study may receive a placebo. 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 was stopped early (reason given: not enough patients (covcid restrictions)). Results are not available in the source record.

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?

The comparison of opioid consumption after physiotherapy, when using VRH or VR sham (time frame: on post operative day 1). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 23 Jul 2021.

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