CClinicalTrials.gg
RecruitingNCT06250582Updated Apr 27, 2025

Does Virtual Reality Improve Symptom Burden in Dialysis Patients?

An interventional study of virtual reality therapy in Dialysis and Virtual Reality, sponsored by David Blum. Recruiting at 1 site in Switzerland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-04-27.

Sponsored by David Blum · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Jul 2025, 1 year 2 months ago, but the record still lists the study as recruiting.
  • Started Dec 2024; still recruiting 1 year 10 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this clinical trial is to investigate the use of virtual reality therapy in dialysis patients. The main question it aims to answer is: Does virtual reality improve symptom burden in dialysis patients and improve their mental wellbeing? Over a period of one month, one virtual reality therapy session of 30 minutes will be performed during each regular hemodialysis session. Since we will conduct a monocentric, crossover randomized controlled trial, the participants act as their own control group.

Read the detailed description

Hemodialysis is a lifesaving therapy for patients with end stage kidney disease but comes with a high burden of physical and emotional symptoms that lower quality of life in dialysis patients. Dialysis mediated complications such as drops in blood pressure, nausea and muscle cramps results in refusal and a negative perception of this treatment. In dialysis patients, treatment-related burden results in deterioration in health related quality of life. During the past few years, Virtual reality (VR) has become more affordable and found its way into households as entertainment electronics but stepwise also into medicine. VR enables the user to view, interact and be immersed in a multisensory 3D virtual world. The aim of the current study is to reduce dialysis-related burden of symptoms by using virtual reality therapy during regular dialysis sessions and thereby improve quality of life among dialysis patients.

02

Conditions studied

  • Dialysis
  • Virtual Reality
03

In context

Lead sponsor

David Blum is the lead sponsor of 2 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Older than 18 years;
  • in treatment with thrice-weekly hemodialysis sessions;
  • regular hemodialysis duration of three to five hours
  • having no visual impairment
  • having no acoustic deficit
  • patient must be capable of speaking and understanding German or English
  • no signs of cognitive impairment
  • patient oriented in time and space
  • being able to give informed consent as documented by signature

Exclusion criteria

Exclusion Criteria:

  • diagnosis of epilepsy
  • current pregnancy
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
20 participants (estimated)

Study arms

  • Experimental
    virtual reality therapy, then standard of care

    During the intervention phase (A) participants will receive virtual reality therapy during their dialysis sessions over a period of one month. After a washout phase of one week, participants will run through a control phase (B, standard of care) also for a period of one month. Subjects will be randomized to an AB or BA sequence.

    Other: virtual reality therapy

  • Experimental
    standard of care, then virtual reality therapy

    During the control phase (B) participants will be treated according to standard of care over a period of one mont. After a washout phase of one week, participants will run through an intervention phase (A) and will receive virtual reality therapy during their dialysis sessions. Also for a period of one month. Subjects will be randomized to an AB or BA sequence.

    Other: virtual reality therapy

Interventions

  • Othervirtual reality therapy

    A virtual reality therapy will be applied for 30 minutes. Patients will be wearing the glasses while lying in bed/chair during their regular dialysis session. Vital signs will be monitored repeatedly. At defined times, patients are asked to answer various questionnaires about their physical and mental health.

06

What researchers measure

Primary outcomes

  1. Reduction of symptom burden of dialysis patients and improvement of their mental wellbeing

    questionnaire

    Time frame: 10 weeks

Secondary outcomes

  1. Evaluation of the effects of virtual reality therapy during hemodialysis on heart rate

    Heart rate (beats per minute)

    Time frame: 10 weeks

  2. Evaluation of the effects of virtual reality therapy during hemodialysis on blood pressure

    Blood pressure (mm Hg)

    Time frame: 10 weeks

  3. To assess the acceptability and appropriateness of using VRT during hemodialysis from the perspectives of patients

    questionnaire

    Time frame: 10 weeks

  4. To assess the acceptability and appropriateness of using VRT during hemodialysis from the perspectives of clinical staff

    questionnaire

    Time frame: 10 weeks

  5. To test the internal consistency of the ESAS-r: Renal Score

    Cronbach's alpha

    Time frame: 10 weeks

07

Study locations

1 of 1 sites recruiting
  • University Hospital Zurich
    Zürich, ZH 8091, Switzerland
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 27, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06250582
Lead sponsor
David Blum
Responsible party
David Blum (Head of the department for Palliative Care of the University hospital Zurich, University of Zurich) — Sponsor-investigator
First posted
Feb 9, 2024
Start date
Dec 2, 2024
Primary completion
Jul 31, 2025 (estimated)
Completion
Dec 31, 2025 (estimated)
Last update
Apr 27, 2025

Study contacts

David Blum, Prof.
Contact
david.blum@usz.ch
+41432533742
STefan Pelz, Dr. med.
Contact
stefan.pelz@usz.ch
+41442553535
David Blum, Prof. Dr.
principal investigator · University of Zurich

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion