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Virtual Reality and Pain Perception During Exercises for Patients With Chronic Non-specific Low Back Pain

The Influence of a Virtual Reality Environment on Pain Perception During Exercises for Patients With Chronic Non-specific Low Back Pain: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02679300
Enrollment
84
Registered
2016-02-10
Start date
2016-01-31
Completion date
2018-09-30
Last updated
2020-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Low Back Pain

Keywords

Chronic Low Back Pain, Virtual Reality, Serious Gaming, Exercise Therapy, Distraction

Brief summary

Immersion in a virtual reality environment has been shown to reduce pain during a variety of painful medical procedures, such as wound care for burn patients and dental care. Often, serious games are used to distract patients from this painful procedures. Recently, serious games have also been developed for patients with low back pain. Because patients with low back pain frequently experience pain during exercises, the investigators hypothesize that exercising with serious games can reduce the pain intensity and the time spent thinking of pain during exercises. To test this hypothesis, the investigators will conduct a randomized controlled trial where two groups will be compared: the experimental group will perform one session of exercises with serious games, while the control group will perform one session of the same exercises without the serious games.

Interventions

OTHERConventional exercise group (control group)
OTHERVirtual reality exercise group

Sponsors

Jessa Hospital
CollaboratorOTHER
Hasselt University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Chronic non-specific low back pain, with or without referred pain to the legs * Age 18-65 * Able to understand Dutch * A minimum pain intensity of 3/10 on the numeric pain rating scale at the time of the test * Being familiar with pelvic tilt exercises

Exclusion criteria

* Spinal surgery in the past * Pregnancy * Serious underlying pathologies (e.g. multiple sclerosis, tumors,…) * Signs or symptoms of nerve root involvement * Known skin-allergy for tape

Design outcomes

Primary

MeasureTime frameDescription
Average pain intensity during exercises using the numeric pain rating scaleDay 1Immediately after the intervention, patients will be asked to indicate the average pain they experienced during the exercises using the numeric pain rating scale (0-10)
Time spent thinking of the pain using a numeric rating scaleDay 1Immediately after the intervention, patients will be asked to indicate the average time they spent thinking of their pain during the exercises using a numeric rating scale ranging from 0 (not at all) to 10 (all the time)

Secondary

MeasureTime frameDescription
Pain intensity after the exercises using a numeric rating scaleDay 1Patients will be asked to indicate their pain immediately after the exercises using the numeric pain rating scale (0-10)
Harmfulness of the exercises using a numeric rating scaleDay 1Immediately after the intervention, patients will be asked to indicate how harmful they thought the exercises were for their lumbar spine on a numeric rating scale ranging from 0 (not harmful at all) to 10 (extremely harmful).

Other

MeasureTime frameDescription
Number of pelvic tiltsDay 1During the exercises the pelvis and lumbar spine of the participants will be recorded with a digital videocamera to capture the number of pelvic tilts during the exercises. This outcome measure will primarily be used as possible covariate
Immersion (questionnaire will be used to measure the level of immersion)Day 1Immediately after the intervention, the immersive experience questionnaire will be used to measure the level of immersion

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026