Citation link: http://dx.doi.org/10.25819/ubsi/10243
DC FieldValueLanguage
crisitem.author.orcid0000-0001-8639-8547-
crisitem.author.orcid0000-0002-0321-6187-
crisitem.author.orcid0000-0002-6923-2526-
crisitem.author.orcid0000-0002-0547-1499-
crisitem.author.orcid0000-0001-9798-1762-
crisitem.author.orcid0000-0001-7558-1274-
crisitem.author.orcid0000-0003-2433-6652-
dc.contributor.authorKampa, Miriam-
dc.contributor.authorBucher, Leandra-
dc.contributor.authorKlapperich, Holger-
dc.contributor.authorMertl, Fabian-
dc.contributor.authorZimmer, Christian-
dc.contributor.authorGeiger, Christian-
dc.contributor.authorHassenzahl, Marc-
dc.contributor.authorFinke, Johannes-
dc.contributor.authorStalder, Tobias-
dc.contributor.authorKlucken, Tim-
dc.date.accessioned2022-12-22T09:32:27Z-
dc.date.available2022-12-22T09:32:27Z-
dc.date.issued2022de
dc.descriptionFinanziert im Rahmen der DEAL-Verträge durch die Universitätsbibliothek Siegende
dc.description.abstractBackground Repeated or chronic stress is considered a major source of disease, in terms of both somatic and mental illnesses. The prevention of stress-related disease by interventions for relaxation has thus increased societal relevance. In this randomized controlled non-inferiority trial, we will compare a newly developed virtual reality (VR) environment for relaxation to an active control group applying a freely chosen relaxation method. To test if our VR environment supports relaxation in a situation of acute stress, a standardized stress induction protocol will precede the relaxation phase. Methods One hundred healthy participants will be recruited from the University of Siegen and randomly assigned to the VR or the active control group that will be free to choose their own relaxation strategy. The multi-sensory VR includes visual, acoustic, and haptic features to induce a strong feeling of presence. The laboratory testing will comprise a baseline measurement, a stress induction, a relaxation intervention, and a recovery measurement. The primary outcomes are self-reported stress and relaxation measured with a visual analog scale (VAS) at pre- and post-baseline, at the start, middle, and end of the stress induction, at pre- and post-relaxation, at pre- and post-recovery, and in the evening of testing. Secondary outcomes are the physiological parameters, namely heart rate and heart rate variability, tonic skin conductance level as well as the number of non-specific skin conductance responses, systolic and diastolic blood pressure and respiratory rate recorded during the four experimental phases as well as state mood, and state rumination assessed at four time points (pre- and post-stress, post-relaxation, and in the evening of testing). Finally, post-event processing will be assessed after relaxation and in the evening of testing. Repeated measures ANOVAs will be performed to test for statistical effects of group, time, and group × time interaction. Discussion The newly developed, multi-sensory VR offers an intervention for relaxation without prior training. Its immersive character might increase efficacy compared to other relaxation methods, especially in situations of acute stress. Future directions could be the development of a mobile version of the VR to enhance accessibility for users. To achieve a transfer of training effects to real life, VR components should successively be eliminated until relaxation is practiced without guidance by the VR.en
dc.identifier.doihttp://dx.doi.org/10.25819/ubsi/10243-
dc.identifier.urihttps://dspace.ub.uni-siegen.de/handle/ubsi/2437-
dc.identifier.urnurn:nbn:de:hbz:467-24376-
dc.language.isoende
dc.sourceTrials ; 23, article number 380. - https://doi.org/10.1186/s13063-022-06307-8de
dc.subject.ddc150 Psychologiede
dc.subject.otherVirtual realityen
dc.subject.otherRelaxationen
dc.subject.otherStress reductionen
dc.subject.otherStress testen
dc.subject.otherRandomized controlled trialde
dc.subject.swbEntspannungstherapiede
dc.subject.swbVirtuelle Realitätde
dc.subject.swbStressbewältigungde
dc.titleFacilitating relaxation and stress reduction in healthy participants through a virtual reality intervention: study protocol for a non-inferiority randomized controlled trialen
dc.typeArticlede
item.fulltextWith Fulltext-
ubsi.publication.affiliationFakultät V - Lebenswissenschaftliche Fakultätde
ubsi.source.doi10.1186/s13063-022-06307-8-
ubsi.source.issn1468-6694-
ubsi.source.issued2022de
ubsi.source.issuenumber23de
ubsi.source.pages12de
ubsi.source.placeLondonde
ubsi.source.publisherBioMed Centralde
ubsi.source.titleTrialsde
ubsi.subject.ghbsHQNde
ubsi.subject.ghbsHQRde
ubsi.subject.ghbsHUFde
ubsi.subject.ghbsHWYMde
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