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Record W4402166321 · doi:10.2196/preprints.65924

Immersive virtual reality improves delayed nausea and depression during paclitaxel/carboplatin or paclitaxel/carboplatin plus bevacizumab therapy: A two-arm randomized controlled trial (Preprint)

2024· preprint· en· W4402166321 on OpenAlexaboutno aff
Kazuyuki Niki, Satoshi Nakagawa, Misaki Arai, Ayaka Morimoto, Yutaka Ueda

Bibliographic record

Venuenot available
Typepreprint
Languageen
FieldMedicine
TopicNausea and vomiting management
Canadian institutionsnot available
Fundersnot available
KeywordsCarboplatinPaclitaxelNauseaPreprintBevacizumabMedicineRandomized controlled trialOncologyInternal medicineComputer scienceChemotherapyWorld Wide WebCisplatin

Abstract

fetched live from OpenAlex

<sec> <title>BACKGROUND</title> Symptomatic drug treatment is generally used to treat various side effects associated with paclitaxel/carboplatin (TC) or TC plus bevacizumab (TC+Bev). However, this can lead to increased adverse effects from additional drugs. Immersive virtual reality (iVR) reduces pain and anxiety. </sec> <sec> <title>OBJECTIVE</title> This study aimed to investigate the efficacy of iVR in managing side effects associated with TC or TC+Bev therapy. </sec> <sec> <title>METHODS</title> This two-arm randomized controlled trial included patients with gynecologic cancer scheduled to undergo their first course of TC/TC+Bev. Patients in the intervention group received iVR for approximately 10 min/day for 7 consecutive days, starting on the first day of treatment. The primary endpoint was the severity of physical and psychiatric symptoms measured using the Japanese version of the revised Edmonton Symptom Rating System (ESAS-r-J). The secondary endpoint included the proportion of patients who used additional antiemetic medications, the complete response (CR) rate to nausea and the severity of anxiety, measured using the state-trait anxiety inventory-JYZ (STAI) Y-1. Patients in the conventional treatment group received supportive and symptomatic treatments. </sec> <sec> <title>RESULTS</title> The analysis included 28 and 30 patients in the intervention and conventional treatment groups, respectively. The change in ESAS-r-J scores between days 1 and 7 and nausea were significantly worse in the intervention group on day 4 only (p&lt;0.001); however, the conventional treatment group showed significantly worse scores on days 3, 4, and 5. Depression was not significantly worse in the intervention group on any day other than on day 1; however, the conventional treatment group showed significantly worse scores on day 4. The proportion of patients who used additional antiemetic medications from days 2 to 7 was significantly lower in the intervention group than in the conventional treatment group (p=0.024). Regarding the change in STAI Y-1 on day 1 of TC or TC+Bev therapy, the mean score was significantly lower after the iVR experience than before the experience in the intervention group (from 43.8 to 34.8, p&lt;0.001), whereas in the conventional treatment group, no significant difference was observed before and after anticancer drug administration (from 44.9 to 43.9, p=0.536). </sec> <sec> <title>CONCLUSIONS</title> iVR may reduce deterioration of nausea and depression more effectively in patients with gynecologic cancer undergoing TC or TC+Bev therapy than in those undergoing conventional treatment, especially in delaying the onset of nausea and accelerating recovery. </sec> <sec> <title>CLINICALTRIAL</title> This study was registered in the UMIN Clinical Trials Registry (UMIN000041067). </sec>

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.006
metaresearch head score (Gemma)0.004
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow), Research integrity
Consensus categoriesMeta-epidemiology (narrow)
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Randomized trial · Consensus signal: Randomized trial
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.036
Threshold uncertainty score0.999

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0060.004
Meta-epidemiology (narrow)0.0020.001
Meta-epidemiology (broad)0.0070.002
Bibliometrics0.0010.000
Science and technology studies0.0000.000
Scholarly communication0.0010.000
Open science0.0010.003
Research integrity0.0010.003
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.024
GPT teacher head0.318
Teacher spread0.294 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; both teacher heads agree on what is shown here.

Study designRandomized trial
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2024
Admission routes1
Has abstractyes

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