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VR for Patients With Chronic Pain (Wait & Work)

U

University of Twente

Status

Completed

Conditions

Chronic Pain

Treatments

Device: VR (Reducept)

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This cluster-RCT evaluates the effect of therapeutic virtual reality (VR) on patients with chronic musculoskeletal pain (CMP) who are on a waiting list to receive pain treatment. The used VR application, Reducept, offers pain education and pain management techniques. This home-based, stand-alone, immersive VR intervention was used daily for four weeks in the intervention group. The control group received standard care (no treatment). Primary outcome measure for this study was health-related quality of life, secondary outcome measures included various pain-related variables (e.g. pain self-efficacy and acceptance. Outcome variables will be measured after four weeks and follow-up after six months.

Enrollment

53 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • aged 18 years or older
  • suffering from primary or secondary CMP
  • finished with biomedical diagnostics and treatment
  • open to biopsychosocial treatment
  • willing and capable of complying with study procedures.

Exclusion criteria

  • not able to finish the VR intervention due to physical (e.g. visual impairment), mental (e.g. severe sensitivity to stimuli) or practical problems (e.g. insufficient tech-literacy)
  • unable to finish Dutch questionnaires.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

53 participants in 2 patient groups

Intervention group
Experimental group
Description:
Four-week, at-home VR intervention with a recommended daily use of 10-30 minutes
Treatment:
Device: VR (Reducept)
Control group
No Intervention group
Description:
No intervention, patient is a waiting-list control

Trial contacts and locations

4

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Central trial contact

Syl Slatman, MSc

Data sourced from clinicaltrials.gov

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