Immersive Virtual Reality eHealth Intervention to Reduce Anxiety and Depression in Pregnant Women: Randomized Controlled Trial.

IF 2.6 Q2 HEALTH CARE SCIENCES & SERVICES
JMIR Human Factors Pub Date : 2025-04-30 DOI:10.2196/71708
Marta Jimenez-Barragan, Amparo Del Pino Gutierrez, Gloria Sauch Valmaña, Olga Monistrol, Carme Monge Marcet, Mar Pallarols Badia, Ignasi Garrido, Anna Carmona Ruiz, Oriol Porta Roda, Cristina Esquinas, Gemma Falguera Puig
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引用次数: 0

Abstract

Background: Mental health during pregnancy is a critical factor influencing maternal and fetal outcomes. Anxiety and depression affect up to 30% of pregnant women, with significant consequences for maternal well-being and child development. Despite this, interventions during pregnancy remain limited, creating a need for innovative, accessible solutions.

Objective: This study aimed to evaluate the effectiveness of an immersive virtual reality (IVR) eHealth intervention in reducing anxiety and depression symptoms in women during pregnancy.

Methods: A 2-arm, randomized controlled trial was conducted across 5 primary care centers in Catalonia, Spain, between October 2021 and May 2024. The study included pregnant women (N=70) aged ≥18 years with moderate anxiety and depression symptoms (Edinburgh Postnatal Depression Scale [EPDS] scores: 9-12) at 12 to 14 weeks of gestation. They were randomly assigned (1:1) to an IVR intervention or standard care group. The intervention group engaged in daily 14-minute IVR mindfulness and relaxation sessions for 6 weeks. Mental health outcomes were assessed using the EPDS and State-Trait Anxiety Inventory.

Results: The intervention group demonstrated significant reductions in EPDS scores, with a mean decrease from 11.32 (SD 0.96) to 7.25 (SD 1.32; P<.001), compared to an increase in the control group from 11.32 (SD 0.94) to 16.23 (SD 1.25; P<.001). Similarly, State-Trait Anxiety Inventory scores improved markedly in the intervention group (mean decrease from 57.94, SD 5.23 to 35.03, SD 6.12; coefficient -30.47, 95% CI -45.23 to -15.72; P<.001), while the control group experienced a nonsignificant increase (from 66.10, SD 5.89 to 72.91, SD 6.34; P=.68). High adherence rates were observed, with 79% (26/33) of participants completing ≥30 sessions. Participant satisfaction was high, with 87% (29/33) reporting being "very satisfied" with the intervention.

Conclusions: The IVR eHealth intervention significantly reduced symptoms of anxiety and depression, demonstrating its potential as an accessible and effective tool for mental health support during pregnancy. High adherence and satisfaction levels underscore its feasibility and acceptability. Future research should explore the long-term effects and scalability of IVR interventions in diverse settings.

Trial registration: ClinicalTrials.gov NCT05756205; https://clinicaltrials.gov/study/NCT05756205.

International registered report identifier (irrid): RR2-10.1186/s12912-023-01440-4.

沉浸式虚拟现实电子健康干预减少孕妇焦虑和抑郁:随机对照试验。
背景:孕期心理健康是影响母胎结局的关键因素。焦虑和抑郁影响着多达30%的孕妇,对孕产妇福祉和儿童发育造成严重后果。尽管如此,怀孕期间的干预措施仍然有限,因此需要创新的、可获得的解决方案。目的:本研究旨在评估沉浸式虚拟现实(IVR)电子健康干预在减少怀孕妇女焦虑和抑郁症状方面的有效性。方法:在2021年10月至2024年5月期间,在西班牙加泰罗尼亚的5个初级保健中心进行了一项两组随机对照试验。本研究纳入年龄≥18岁、妊娠12 ~ 14周伴有中度焦虑和抑郁症状(爱丁堡产后抑郁量表[EPDS]评分:9-12)的孕妇(N=70)。他们被随机分配(1:1)到IVR干预组或标准护理组。干预组每天进行14分钟的IVR正念和放松课程,持续6周。使用EPDS和状态-特质焦虑量表评估心理健康结果。结果:干预组EPDS评分显著降低,平均由11.32分(SD 0.96)降至7.25分(SD 1.32;结论:IVR电子健康干预显著减少了焦虑和抑郁症状,显示了其作为孕期心理健康支持的一种可获得和有效的工具的潜力。高依从性和满意度水平强调了其可行性和可接受性。未来的研究应该探索IVR干预在不同环境下的长期效果和可扩展性。试验注册:ClinicalTrials.gov NCT05756205;https://clinicaltrials.gov/study/NCT05756205.International注册报告标识符(irrid): RR2-10.1186/s12912-023-01440-4。
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
JMIR Human Factors
JMIR Human Factors Medicine-Health Informatics
CiteScore
3.40
自引率
3.70%
发文量
123
审稿时长
12 weeks
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