评估增强现实技术在缓解儿童口服注射期间的焦虑和疼痛中的应用:一项随机对照试验。

IF 2
M Albaal, N Bshara
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引用次数: 0

摘要

目的:本研究评估增强现实(AR)耳机在减少儿童(7-9 岁)口服注射期间焦虑和疼痛的有效性。方法:将108名儿童随机分为4组:对照组(注射时在移动设备上观看卡通)、 a组(注射时通过AR耳机观看卡通)、 B组(转移到牙科椅前进行AR游戏)和 C组(注射前进行AR游戏加卡通)。采用Venham’s Picture Test (VPT)和心率(HR)监测评估焦虑程度;采用FLACC行为疼痛评定量表和Wong-Baker FACES疼痛评定量表测量疼痛。结果:注射后,A组(46.59)、B组(42.83)和C组(40.41)的VPT平均排名明显低于对照组(65.17);P结论:AR头显可显著降低儿童注射相关焦虑,消除儿童剧烈疼痛行为,为儿科牙科医生提供了一种低成本、易于实施的工具,提高患者的舒适度和配合度。该研究已在ClinicalTrials.gov注册(NCT06724341)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluating the use of augmented reality in alleviating anxiety and pain in children during intraoral injection administration: a randomized-controlled trial.

Purpose: This study evaluated augmented reality (AR) headsets' effectiveness in reducing anxiety and pain in children (7-9 years) during intraoral injections.

Methods: One hundred eight children were randomized to four groups: Control (cartoons on a mobile device during injection), Group A (cartoons via AR headset during injection), Group B (AR games before being transported to the dental chair), and Group C (AR games before plus cartoons during injection). Anxiety was assessed by Venham's Picture Test (VPT) and heart rate (HR) monitoring; pain was measured with the FLACC Behavioral Pain Assessment Scale and the Wong-Baker FACES Pain Rating Scale.

Results: Post-injection, VPT mean ranks were significantly lower in Groups A (46.59), B (42.83), and C (40.41) compared to the Control group (65.17; P < 0.05). HR monitoring revealed a significant increase during injection in the Control group (107.6 ± 15.7 bpm) and Group A (106.6 ± 13.2 bpm) compared with Groups B (94.7 ± 8.0 bpm) and C (91.4 ± 9.8 bpm; P < 0.05). Severe pain (WBF score ≥ 8) was reported by 18.5% in the Control group versus none in the test groups (P < 0.05). Similarly, FLACC scores indicated the highest discomfort in the Control group, with no severe discomfort observed in Groups A, B, or C (P < 0.05).

Conclusions: AR headsets significantly reduce injection-related anxiety and eliminate severe pain behaviors in children, providing pediatric dental practitioners with a low-cost, easily implemented tool to enhance patient comfort and cooperation. The study was registered at ClinicalTrials.gov (NCT06724341).

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