Evidence map›Paper›PMID 35812818›Full record

ArticleContemporary clinical trials communications2022

Immersive virtual reality in a northern Queensland haemodialysis unit: Study protocol for a cross-over randomized controlled feasibility trial (ACTRN12621000732886).

Wendy Smyth, Joleen McArdle, John Body-Dempsey, Valli Manickam, Anne Swinbourne, Ickjai Lee, Jason Holdsworth, Olumuyiwa Omonaiye, Cate Nagle

Abstract read
In one paragraph

Article in Contemporary clinical trials communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Wendy SmythTownsville Hospital and Health Service, PO Box 670, Townsville, Queensland, 4810, Australia.
Joleen McArdleTownsville Hospital and Health Service, PO Box 670, Townsville, Queensland, 4810, Australia.
John Body-DempseyTownsville Hospital and Health Service, PO Box 670, Townsville, Queensland, 4810, Australia.
Valli ManickamTownsville Hospital and Health Service, PO Box 670, Townsville, Queensland, 4810, Australia.
Anne SwinbourneCollege of Healthcare Sciences, James Cook University, Townsville, Queensland, 4811, Australia.
Ickjai LeeCollege of Science & Engineering, James Cook University, Cairns, Queensland, 4878, Australia.
Jason HoldsworthCollege of Science & Engineering, James Cook University, Cairns, Queensland, 4878, Australia.
Olumuyiwa OmonaiyeCollege of Healthcare Sciences, James Cook University, Townsville, Queensland, 4811, Australia.
Cate NagleTownsville Hospital and Health Service, PO Box 670, Townsville, Queensland, 4810, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Despite being a life-preserving medical treatment, the demands of haemodialysis are a significant impost on individuals, posing considerable burdens on their work, vocational activities and involvement with family and community. In our region, patients who have had to relocate considerable distances to a regional city for dialysis, and First Nations people, are less likely to attend all scheduled dialysis sessions. Virtual reality (VR) has been shown to improve engagement with care of people on haemodialysis.This manuscript describes the protocol for a cross-over randomised controlled trial (RCT) that will explore the impact of an immersive VR experience for patients attending a northern Queensland, Australia, haemodialysis service. Methods: The design is a crossover RCT, with 8 clusters according to haemodialysis location and schedule. Clusters (5 participants in each) will be randomized by computer program. Participants in the trial will be patients who undergo haemodialysis three times/week at one of two dialysis units. During the 4-week intervention period (12 haemodialysis sessions), participants will be provided a headset with vision representative of the natural environment, and with audio. The 4-week control period will comprise usual activities, such as watching television, reading and sleeping. Outcomes will be measured by participants': attendance at scheduled dialysis sessions; adherence to lifestyle modifications; wellbeing, anxiety and depression; acceptability and usability of VR; and adverse events such as nausea. The feasibility and acceptability of the intervention from clinicians' perspectives will also be explored. Discussion: If this VR intervention is feasible, then participants may engage more with haemodialysis regimens and self-care in this very clinical environment. Trial registration: ACTRN12621000732886.

Identifiers

PMID35812818
PMCPMC9256545

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.