{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,27]],"date-time":"2026-02-27T20:17:46Z","timestamp":1772223466694,"version":"3.50.1"},"reference-count":29,"publisher":"Public Library of Science (PLoS)","issue":"7","license":[{"start":{"date-parts":[[2025,7,7]],"date-time":"2025-07-07T00:00:00Z","timestamp":1751846400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["www.plosone.org"],"crossmark-restriction":false},"short-container-title":["PLoS One"],"abstract":"<jats:sec id=\"sec001\">\n                    <jats:title>Introduction<\/jats:title>\n                    <jats:p>Virtual reality (VR) has increasingly found applications beyond leisure and video games, extending into the field of medicine. Recent studies indicate that VR can effectively reduce anxiety and pain in pediatric patients undergoing uncomfortable medical procedures, such as burn wound care. Yet, VR use in the operating room is still rare, despite a growing trend toward regional anesthesia without general anesthesia; physicians still frequently rely on pharmacological sedation to manage procedural anxiety. By leveraging VR\u2019s anxiolytic properties, it may be possible to decrease the need for intravenous (IV) sedation which is associated with risk of adverse events like apnea and hypoxemia and delayed recovery.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"sec002\">\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>This study\u2019s main objective is to determine the impact of VR on IV sedation requirements in adult patients undergoing breast surgery under paravertebral (PV) block without general anesthesia. We will be using Paperplane Therapeutics\u2019 VR headset and software which offer three distinct VR scenario choices. We hypothesize that VR immersion will reduce the need for intraoperative pharmacological sedation. Secondary objectives include assessing the tolerance of patients to the VR headset, examining the impact of the chosen VR scenario on the primary outcome, evaluating the incidence of adverse effects, measuring patient satisfaction, and analyzing the output of the Nociception Level (NOL) Index among awake surgical patients.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"sec003\">\n                    <jats:title>Materials and methods<\/jats:title>\n                    <jats:p>This single center randomized controlled trial will enroll 100 patients aged 18 or above undergoing breast surgery under PV block. Participants will be randomly allocated to the VR group or the control group; both will have access to pharmacological sedation through patient-controlled sedation (PCS). Participants in the VR group will choose between three different VR scenarios and will be allowed to switch between these scenarios during surgery. The primary outcome will be the time-adjusted and weight adjusted dose of self-administered intraoperative propofol. Secondary outcomes will include patient satisfaction, adverse events, and post-anesthesia care unit length of stay (PACU LOS).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"sec004\">\n                    <jats:title>Ethics<\/jats:title>\n                    <jats:p>\n                      This trial has been approved by the regional ethics committee (Comit\u00e9 d\u2019\u00c9thique de la Recherche du CIUSSS de l\u2019Est de l\u2019\u00cele de Montr\u00e9al) on September 9\n                      <jats:sup>th<\/jats:sup>\n                      , 2024.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"sec005\">\n                    <jats:title>Trial registration<\/jats:title>\n                    <jats:p>ClinicalTrials.gov (July 25th, 2024). Unique protocol ID: 2025\u20133802. Trial identification number: NCT06522711.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1371\/journal.pone.0327555","type":"journal-article","created":{"date-parts":[[2025,7,7]],"date-time":"2025-07-07T13:23:07Z","timestamp":1751894587000},"page":"e0327555","update-policy":"https:\/\/doi.org\/10.1371\/journal.pone.corrections_policy","source":"Crossref","is-referenced-by-count":0,"title":["Virtual reality as a strategy for intra-operatory anxiolysis and pharmacological sparing in patients undergoing breast surgeries: The V-RAPS randomized controlled trial protocol"],"prefix":"10.1371","volume":"20","author":[{"ORCID":"https:\/\/orcid.org\/0009-0008-6009-3540","authenticated-orcid":true,"given":"Joe","family":"Zako","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nicolas","family":"Daccache","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Julien","family":"Burey","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ariane","family":"Clairoux","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Louis","family":"Morisson","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-3347-1581","authenticated-orcid":true,"given":"Pascal","family":"Laferri\u00e8re-Langlois","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"340","published-online":{"date-parts":[[2025,7,7]]},"reference":[{"key":"pone.0327555.ref001","doi-asserted-by":"crossref","first-page":"1273631","DOI":"10.3389\/frobt.2023.1273631","article-title":"Smart haptic gloves for virtual reality surgery simulation: a pilot study on external ventricular drain training","volume":"10","author":"J Boutin","year":"2024","journal-title":"Front Robot AI"},{"key":"pone.0327555.ref002","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1016\/j.janxdis.2018.08.003","article-title":"Virtual reality exposure therapy for anxiety and related disorders: a meta-analysis of randomized controlled trials","volume":"61","author":"E Carl","year":"2019","journal-title":"J Anxiety Disord"},{"issue":"1","key":"pone.0327555.ref003","doi-asserted-by":"crossref","first-page":"52","DOI":"10.1007\/s10143-023-02260-5","article-title":"Assessing the benefits of digital twins in neurosurgery: a systematic review","volume":"47","author":"S Chumnanvej","year":"2024","journal-title":"Neurosurg Rev"},{"issue":"1","key":"pone.0327555.ref004","article-title":"Virtual reality and surgical simulation training for orthopaedic surgery residents: a qualitative assessment of trainee perspectives","volume":"9","author":"AW Kuhn","year":"2024","journal-title":"JB JS Open Access"},{"issue":"1","key":"pone.0327555.ref005","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1016\/j.jsurg.2023.11.012","article-title":"A systematic review of immersive virtual reality for nontechnical skills training in surgery","volume":"81","author":"WS Yi","year":"2024","journal-title":"J Surg Educ"},{"issue":"4","key":"pone.0327555.ref006","doi-asserted-by":"crossref","first-page":"741","DOI":"10.1097\/j.pain.0000000000003086","article-title":"Can virtual reality enhance the patient experience during awake invasive procedures? 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