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Not yet recruiting NCT06739187

Virtual Reality for Cognitive Impairment in Hemodialysis

Phase II Interventional Hemodialysis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Virtual reality platform on head mounted display.
Who it may be relevant to
Registry conditions: Hemodialysis. Basic parameters: 18 years — 75 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Virtual Reality Training for Cognitive Impairment in Adults Treated With Hemodialysis: A Feasibility Randomized Controlled Trial

Overview

The goal of this randomized feasibility clinical trial is to identify participant recruitment and retention, acceptability, and adherence to virtual reality training in people undergoing hemodialysis. The main question it aims to answer is if virtual reality could be a feasible and acceptable intervention in this setting. The investigators will compare participants on virtual reality training during the standard dialysis session with those treated with standard dialysis session alone to see if a cognitive training using immersive virtual reality in people on hemodialysis is feasible and acceptable. Participants randomised in the intervention group will use virtual reality during the standard dialysis session for 30 minutes, three times a week for 12 weeks. The virtual reality intervention will consist of computerized cognitive training of 4 games. Each exercise delivered to the participant will specifically provide training in a specific cognitive category (memory, cognitive flexibility, processing, attention, and memory). Participants randomised in the control group will perform the standard hemodialysis session three times a week for 12 weeks, without using virtual reality.

Detailed description

The trial is a multicenter, parallel group, feasibility randomized controlled trial.

The trial population will include adult participants, who have the physical and cognitive capacity to be trained using immersive virtual reality and who have kidney failure on hemodialysis.

Participants will be allocated in the intervention (virtual reality session) or standard of care without the intervention. Participants will be allocated to intervention or standard care by randomization 1:1.

The virtual reality intervention will consist of computerized cognitive training of a subset of 4 short, gamified exercises. The intervention will be accessed through the Enhance VR platform on a Meta Quest 3S head mounted display, Snapdragon XR2 Gen2, processor, 8 Gb RAM, 128 Gb internal memory, resolution per eye in pixels: 1832 x 1920 with a refresh rate of 90-120 Hz and motion controllers. The clinician responsible for the intervention will be in the room with the participant, providing support for the intervention and any technical issues.

The chosen trial duration of 12 weeks is designed to provide exposure to a meaningful dose of cognitive training (three times a week) aligned to previous similar studies and to maximize participant tolerability to immersive virtual reality training.

The endpoints described in this protocol align with the recommendations of the CONSORT 2010 statement: extension to randomized pilot and feasibility studies. The endpoints are specifically chosen to relate to feasibility. The outcomes also include the primary and secondary outcomes for the future definitive randomized controlled trial to assess response, feasibility of measurement, and completeness.

Interventions

  • Device Virtual reality platform on head mounted display
    Enhance Virtual Reality platform on a Meta Quest head mounted display

Primary outcome measures

  • Accept the invitation to participate [Time frame: 4, 12 weeks]
  • Appropriateness of eligibility criteria [Time frame: 12 weeks]
  • Retention [Time frame: 12 weeks]
  • Acceptability [Time frame: 12 weeks]
  • Proportion of adverse events [Time frame: 12 weeks]
  • Quality of life [Time frame: 0, 4, 12, 24 weeks]
Secondary outcome measures (12)
  • Depression [Time frame: 0, 4, 12, 24 weeks]
  • Anxiety [Time frame: 0, 4, 12, 24 weeks]
  • Quality of life [Time frame: 0, 4, 12, 24 weeks]
  • Fatigue [Time frame: 0, 4, 12, 24 weeks]
  • Health utility [Time frame: 0 and 12 weeks]
  • All-cause death [Time frame: 12 weeks]
  • Cardiovascular events [Time frame: 12 weeks]
  • Pulse [Time frame: 0 and 12 weeks]
  • Systolic blood pressure [Time frame: 0 and 12 weeks]
  • Diastolic blood pressure [Time frame: 0 and 12 weeks]
  • Functional near-infrared spectroscopy [Time frame: 0 and 12 weeks]
  • Kt/V [Time frame: 0 and 12 weeks]

Eligibility criteria

Inclusion criteria

  • Adult participants aged 18 years or older and less than or equal to 75 years of age
  • Receiving haemodialysis treatment for kidney failure for at least 90 days (permanent reduction in kidney function below an estimated glomerular filtration rate of 15 mL/minute per 1.73 m2)
  • Able to provide written and informed consent
  • Able to use the immersive virtual reality headset and follow instructions with sufficient motor, visual and auditory function to interact with the intervention
  • Able to speak and understand Italian language

Exclusion criteria

  • Severe cognitive impairment or psychiatric diseases leading to inability to follow instructions and use the virtual reality headset
  • Significant nystagmus and/or vertigo leading to inability to tolerate the virtual reality headset
  • Insufficient motor function to use the virtual reality system
  • Hearing or visual disability
  • Advanced or uncompensated chronic diseases unrelated to kidney failure (e.g. advanced cancer, heart failure, lung diseases with poor oxygen saturation)
  • Other neurological diseases (ictus, Alzheimer's or other forms of dementia)
  • Persistent pain or itch or who using opioids that may interfere with the tests or any other condition that the clinician may judge as influencing the results

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Italy · 2 centers
  • University of Bari — Bari
  • Univerity Vanvitelli — Naples

Publications

  • Viggiano D, Pellegrino G, Natale P, Buonincontri V, Gigliotti G, Genualdo R, Nappi F, De Nicola L, Iodice C, Iannuzzi M, Iulianiello P, Auricchio MR, Zamboli P, Montinaro V, Strippoli G. Virtual reality training for cognitive impairment in adults treated with haemodialysis (VIRTUAL): protocol for a multicentre, randomised, open-label feasibility trial. BMJ Open. 2026 Jun 28;16(6):e120700. doi: 10. PMID 42366016

Identifiers

NCT: NCT06739187 · PRIN20225JEHW8 · PRIN20225JEHW8

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗