Expected benefits and concerns regarding virtual reality in caring for terminally ill cancer patients - a qualitative interview study.

IF 2.5 2区 医学 Q2 HEALTH CARE SCIENCES & SERVICES BMC Palliative Care Pub Date : 2024-11-04 DOI:10.1186/s12904-024-01557-6
Anja Greinacher, Bernd Alt-Epping, Christina Gerlach, Cornelia Wrzus
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Abstract

Background: Many palliative cancer patients require inpatient hospital treatment for medical reasons, which contrasts their frequent desire to be at home. Virtual reality (VR) could be a way of bringing the home environment closer to them. First observations have shown benefits from VR for inpatients in palliative care. The aim of this qualitative, descriptive study was to explore the expectations of in-patients suffering from incurable cancer and their relatives about VR, in particular individualized VR images of the patients' own home.

Methods: Semi-structured interviews with inpatients suffering from incurable cancers and their relatives in three medical settings (palliative care, hematology, radiotherapy) of a German university hospital. Qualitative content analysis about expected benefits and concerns regarding VR-videos showing their private home; defining the main topics deductively and the subcategories inductively. We also assessed the patients' subjective perspective on their remaining time to live to estimate the impact of double awareness on the results. The Patient Advisory Board informed the study protocol and conduct.

Results: We interviewed 15 patients (8 men; age M = 63.4, SD = 11.34; range 39-82) under palliative care, and four relatives. We organized the interview content in 6 themes (general interest, desired content, non-desired content, expected benefits, concerns, and irregularities) and 26 sub-themes. Most patients and relatives were interested in using VR during hospital treatment. They often preferred viewing nature or tourist sites over seeing their home or family. Reasons could be linked to privacy concerns and the general desire for distraction from the current situation that they specified with their expectation of well-being, a break from the patient-experience, the pursue of curiosity, and the VR evoking fond memories.

Conclusion: VR seems to be of interest for palliative cancer patients, especially as distraction and relief from their illness. The desired content can be very different, so a choice from a selection of VR-content should be made available. If patients want to see videos of their own home, recordings by relatives instead of study or hospital staff seem to meet the need for privacy.

Trial registration: Registered at Deutsches Register Klinischer Studien; registration number: DRKS00032172; registration date: 11/07/2023. https://drks.de/search/de/trial/DRKS00032172.

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虚拟现实技术在护理癌症晚期患者方面的预期益处和担忧--定性访谈研究。
背景:许多姑息治疗癌症患者由于医疗原因需要住院治疗,这与他们经常希望在家的愿望形成鲜明对比。虚拟现实(VR)可以让他们更接近家庭环境。初步观察显示,虚拟现实技术对姑息治疗的住院病人大有裨益。这项描述性定性研究的目的是探讨患有不治之症的癌症住院患者及其亲属对 VR 的期望,特别是患者家中的个性化 VR 图像:方法:在德国一所大学医院的三个医疗场所(姑息治疗、血液科、放射治疗)对患有不治之症的癌症住院患者及其亲属进行半结构式访谈。通过定性内容分析,了解患者对显示其私人住宅的 VR 视频的预期益处和担忧;通过演绎法确定主要议题,通过归纳法确定子类别。我们还评估了患者对其剩余生存时间的主观看法,以估计双重意识对结果的影响。患者咨询委员会对研究方案和实施进行了指导:我们对 15 名接受姑息治疗的患者(8 名男性;年龄 M = 63.4,SD = 11.34;范围 39-82)和 4 名亲属进行了访谈。我们将访谈内容归纳为 6 个主题(一般兴趣、期望内容、非期望内容、预期益处、担忧和异常)和 26 个子主题。大多数患者和亲属都对在医院治疗期间使用 VR 感兴趣。他们通常更喜欢观看大自然或旅游景点,而不是看自己的家或家人。其中的原因可能与隐私问题有关,也可能与他们普遍希望从当前的状况中转移注意力有关,他们希望从病人的经历中解脱出来,追求好奇心,以及 VR 能唤起美好的回忆:结论:VR 似乎对癌症姑息治疗患者很有吸引力,尤其是可以分散他们的注意力,缓解他们的病痛。所需的内容可能大相径庭,因此应提供可供选择的 VR 内容。如果患者希望观看自己家中的视频,由亲属而非研究人员或医院工作人员录制的视频似乎更能满足患者的隐私需求:试验注册:在德国临床研究注册中心注册;注册号:DRKS00032172;注册号:DRKS00032172:DRKS00032172;注册日期:2023 年 7 月 11 日。https://drks.de/search/de/trial/DRKS00032172。
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来源期刊
BMC Palliative Care
BMC Palliative Care HEALTH CARE SCIENCES & SERVICES-
CiteScore
4.60
自引率
9.70%
发文量
201
审稿时长
21 weeks
期刊介绍: BMC Palliative Care is an open access journal publishing original peer-reviewed research articles in the clinical, scientific, ethical and policy issues, local and international, regarding all aspects of hospice and palliative care for the dying and for those with profound suffering related to chronic illness.
期刊最新文献
Communication about incurable illness and remaining life between spouses and patients with incurable illness receiving specialized home care: effects of a family caregiver-targeted web-based psycho-educational intervention. Correction: Adapting the serious illness conversation guide for unhoused older adults: a rapid qualitative study. Online education in palliative care - A national exploratory multimethod study. The family talk intervention prevent the feeling of loneliness - a long term follow up after a parents life-threatening illness. Is the use of antibiotic stewardship measures in the context of specialized outpatient palliative care sensible and feasible? An interview-based study.
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