Feasibility, acceptability, patient experience, and preliminary efficacy of a virtual reality guided imagery intervention for chronic pain.

IF 3.2 Q1 HEALTH CARE SCIENCES & SERVICES
Frontiers in digital health Pub Date : 2025-06-24 eCollection Date: 2025-01-01 DOI:10.3389/fdgth.2025.1505861
Lauren Doan, Marc Recasens, Jessica Lake, Ian Miller, Elise Vierra, Steven Richeimer, Iris Yao, Doerte U Junghaenel, Faye Weinstein
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引用次数: 0

Abstract

Objectives: Guided imagery is a strategy utilized in chronic pain management by patients. Benefits are cumulative via ongoing application. Engagement via Virtual Reality (VR) is becoming more accessible as a strategy to enhance adherence, use and benefit of guided imagery. We conducted a preliminary investigation of the feasibility, acceptability, patient experience, and efficacy of the use of VR for patients with chronic pain to use at home.

Methods: 36 patients with Complex Regional Pain Syndrome or Low Back Pain were randomly assigned to VR or audio only guided imagery groups. Feasibility, acceptability and patient experience were rated by participants. Outcomes assessed at baseline and post-intervention were pain, mental and physical health, and mood.

Results: Results indicate that the intervention was feasible and found acceptable by participants. The intervention also demonstrated promising preliminary efficacy based on self-reported within-group decreases in pain, depressive symptoms, anxiety symptoms and improvements in physical and mental functioning.

Conclusions: The use of VR shows promise for enhancing the application and experience of guided imagery training with people who have chronic pain.

虚拟现实引导图像干预慢性疼痛的可行性、可接受性、患者体验和初步疗效。
目的:引导成像是一种用于慢性疼痛患者管理的策略。福利是通过持续申请累积的。通过虚拟现实(VR)参与正成为一种更容易获得的策略,以增强对引导图像的依从性、使用和益处。我们对慢性疼痛患者在家中使用VR的可行性、可接受性、患者体验和疗效进行了初步调查。方法:36例复杂区域性疼痛综合征或腰痛患者随机分为VR组和单纯音频引导成像组。参与者对可行性、可接受性和患者体验进行评分。基线和干预后评估的结果是疼痛、身心健康和情绪。结果:干预措施是可行的,被患者接受。基于组内自我报告的疼痛、抑郁症状、焦虑症状的减少以及身体和精神功能的改善,干预也显示出有希望的初步效果。结论:VR的使用有望增强慢性疼痛患者的引导图像训练的应用和体验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.20
自引率
0.00%
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审稿时长
13 weeks
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