Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/116978
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dc.contributorDepartment of Language Science and Technology-
dc.creatorWong, WWS-
dc.creatorWong, GHY-
dc.creatorChoy, JCP-
dc.creatorLi, DSP-
dc.creatorLo, YL-
dc.date.accessioned2026-01-21T03:54:31Z-
dc.date.available2026-01-21T03:54:31Z-
dc.identifier.urihttp://hdl.handle.net/10397/116978-
dc.language.isoenen_US
dc.publisherPublic Library of Scienceen_US
dc.rightsCopyright: © 2025 Wong et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en_US
dc.rightsThe following publication Wong WWS, Wong GHY, Choy JCP, Pui Li DS, Lo YL (2025) Utilization of Immersive Virtual Reality in Cognitive Stimulation Therapy (IVR-CST) for elderly with mild cognitive impairment: A randomized controlled pilot study protocol. PLoS One 20(8): e0330686 is available at https://doi.org/10.1371/journal.pone.0330686.en_US
dc.titleUtilization of Immersive Virtual Reality in Cognitive Stimulation Therapy (IVR-CST) for elderly with mild cognitive impairment : a randomized controlled pilot study protocolen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume20-
dc.identifier.issue8-
dc.identifier.doi10.1371/journal.pone.0330686-
dcterms.abstractObjectives: Mild cognitive impairment (MCI) affects about 11.4% of the elderly population in Hong Kong. This study mainly investigates the feasibility and efficacy of immersive virtual reality-based cognitive stimulation therapy (IVR-CST) on MCI, and the use of eye-tracking technology in studying treatment outcome.-
dcterms.abstractHypothesis to be tested: 1) Whether IVR-CST is a feasible intervention for the elderly with MCI. 2) Whether IVR-CST is efficacious (and more efficacious than conventional CST) in improving cognition. 3) Whether changes in eye movements across therapy and treatment outcome are associated.-
dcterms.abstractDesign and subjects: An open-label, two-armed, assessor-blinded, randomized controlled trial will be conducted. Sixty-six elderly individuals with MCI will be recruited and randomly allocated to either the IVR-CST or the conventional CST group. Their cognition will be measured before and immediately after therapy and 4 weeks post-therapy.-
dcterms.abstractInterventions: A 14-session IVR-CST or conventional CST, with content adapted from the Chinese-translated manual of CST, will be carried out twice per week in groups of three to four individuals.-
dcterms.abstractOutcome measures and data analysis: The Hong Kong Montreal Cognitive Assessment and measures on executive functions/working memory will serve as primary outcomes. The within-subject (before and after therapy) and between-subject (IVR-CST vs. conventional CST) differences will be examined. Besides, eye movements during therapy in the IVR-CST group will be collected and its correlation with primary outcomes will be studied.-
dcterms.abstractExpected results: Positive changes in cognition are expected after therapy in both treatment groups, which may be maintained four weeks post-therapy.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationPLoS one, 2025, v. 20, no. 8, e0330686-
dcterms.isPartOfPLoS one-
dcterms.issued2025-
dc.identifier.scopus2-s2.0-105014124559-
dc.identifier.pmid40857307-
dc.identifier.eissn1932-6203-
dc.identifier.artne0330686-
dc.description.validate202601 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe project is supported by the Health and Medical Research Fund of the Health Bureau of the Hong Kong Special Administrative Region of the People’s Republic of China (grant reference number: 22231471).en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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