Cargando…

Facilitating relaxation and stress reduction in healthy participants through a virtual reality intervention: study protocol for a non-inferiority randomized controlled trial

BACKGROUND: 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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kampa, Miriam, Finke, Johannes, Stalder, Tobias, Bucher, Leandra, Klapperich, Holger, Mertl, Fabian, Zimmer, Christian, Geiger, Christian, Hassenzahl, Marc, Klucken, Tim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082920/
https://www.ncbi.nlm.nih.gov/pubmed/35534868
http://dx.doi.org/10.1186/s13063-022-06307-8
_version_ 1784703307833409536
author Kampa, Miriam
Finke, Johannes
Stalder, Tobias
Bucher, Leandra
Klapperich, Holger
Mertl, Fabian
Zimmer, Christian
Geiger, Christian
Hassenzahl, Marc
Klucken, Tim
author_facet Kampa, Miriam
Finke, Johannes
Stalder, Tobias
Bucher, Leandra
Klapperich, Holger
Mertl, Fabian
Zimmer, Christian
Geiger, Christian
Hassenzahl, Marc
Klucken, Tim
author_sort Kampa, Miriam
collection PubMed
description BACKGROUND: 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. TRIAL REGISTRATION: ISRCTN Registry ISRCTN11162338. Retrospectively registered on January 22, 2021
format Online
Article
Text
id pubmed-9082920
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-90829202022-05-10 Facilitating relaxation and stress reduction in healthy participants through a virtual reality intervention: study protocol for a non-inferiority randomized controlled trial Kampa, Miriam Finke, Johannes Stalder, Tobias Bucher, Leandra Klapperich, Holger Mertl, Fabian Zimmer, Christian Geiger, Christian Hassenzahl, Marc Klucken, Tim Trials Study Protocol BACKGROUND: 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. TRIAL REGISTRATION: ISRCTN Registry ISRCTN11162338. Retrospectively registered on January 22, 2021 BioMed Central 2022-05-09 /pmc/articles/PMC9082920/ /pubmed/35534868 http://dx.doi.org/10.1186/s13063-022-06307-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Study Protocol
Kampa, Miriam
Finke, Johannes
Stalder, Tobias
Bucher, Leandra
Klapperich, Holger
Mertl, Fabian
Zimmer, Christian
Geiger, Christian
Hassenzahl, Marc
Klucken, Tim
Facilitating relaxation and stress reduction in healthy participants through a virtual reality intervention: study protocol for a non-inferiority randomized controlled trial
title Facilitating relaxation and stress reduction in healthy participants through a virtual reality intervention: study protocol for a non-inferiority randomized controlled trial
title_full Facilitating relaxation and stress reduction in healthy participants through a virtual reality intervention: study protocol for a non-inferiority randomized controlled trial
title_fullStr Facilitating relaxation and stress reduction in healthy participants through a virtual reality intervention: study protocol for a non-inferiority randomized controlled trial
title_full_unstemmed Facilitating relaxation and stress reduction in healthy participants through a virtual reality intervention: study protocol for a non-inferiority randomized controlled trial
title_short Facilitating relaxation and stress reduction in healthy participants through a virtual reality intervention: study protocol for a non-inferiority randomized controlled trial
title_sort facilitating relaxation and stress reduction in healthy participants through a virtual reality intervention: study protocol for a non-inferiority randomized controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082920/
https://www.ncbi.nlm.nih.gov/pubmed/35534868
http://dx.doi.org/10.1186/s13063-022-06307-8
work_keys_str_mv AT kampamiriam facilitatingrelaxationandstressreductioninhealthyparticipantsthroughavirtualrealityinterventionstudyprotocolforanoninferiorityrandomizedcontrolledtrial
AT finkejohannes facilitatingrelaxationandstressreductioninhealthyparticipantsthroughavirtualrealityinterventionstudyprotocolforanoninferiorityrandomizedcontrolledtrial
AT staldertobias facilitatingrelaxationandstressreductioninhealthyparticipantsthroughavirtualrealityinterventionstudyprotocolforanoninferiorityrandomizedcontrolledtrial
AT bucherleandra facilitatingrelaxationandstressreductioninhealthyparticipantsthroughavirtualrealityinterventionstudyprotocolforanoninferiorityrandomizedcontrolledtrial
AT klapperichholger facilitatingrelaxationandstressreductioninhealthyparticipantsthroughavirtualrealityinterventionstudyprotocolforanoninferiorityrandomizedcontrolledtrial
AT mertlfabian facilitatingrelaxationandstressreductioninhealthyparticipantsthroughavirtualrealityinterventionstudyprotocolforanoninferiorityrandomizedcontrolledtrial
AT zimmerchristian facilitatingrelaxationandstressreductioninhealthyparticipantsthroughavirtualrealityinterventionstudyprotocolforanoninferiorityrandomizedcontrolledtrial
AT geigerchristian facilitatingrelaxationandstressreductioninhealthyparticipantsthroughavirtualrealityinterventionstudyprotocolforanoninferiorityrandomizedcontrolledtrial
AT hassenzahlmarc facilitatingrelaxationandstressreductioninhealthyparticipantsthroughavirtualrealityinterventionstudyprotocolforanoninferiorityrandomizedcontrolledtrial
AT kluckentim facilitatingrelaxationandstressreductioninhealthyparticipantsthroughavirtualrealityinterventionstudyprotocolforanoninferiorityrandomizedcontrolledtrial