青少年社交焦虑症状的移动心理教育项目(OkeyMind)的有效性和成本效益:一项随机对照试验方案。

IF 1.4 Q3 HEALTH CARE SCIENCES & SERVICES
Yi-Zhou Wang, De-Hui Ruth Zhou, Siu-Man Ng, Bei-Bei Wang, Yu-Ya Feng, Xue Weng
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引用次数: 0

摘要

背景:社交焦虑在青少年中越来越普遍,导致社交退缩、孤立和抑郁风险增加。移动医疗(mHealth)干预措施提供匿名性、可及性和个性化支持,但其对患有社交焦虑的年轻人的有效性和成本效益尚不清楚。目的:本随机对照试验旨在评估基于移动的心理教育项目(OkeyMind)减轻青少年社交焦虑症状的有效性和成本效益。方法:招募15 ~ 24岁轻度及以上重度社交恐惧症(social phobia Inventory [SPIN]≥25)、可使用微信的参与者,进行现场筛选,随机分为干预组或等候组。这项研究将招募180名参与者,每组90人。干预组将接受为期1个月的移动心理教育项目(OkeyMind),该项目包括心理教育和冥想两部分,所有内容都是全自动的。等待名单对照组将在3个月后接受同样的干预。主要结局是使用SPIN测量社交焦虑症状。次要结局包括抑郁(患者健康问卷-9)和健康相关生活质量(EuroQol-5)。评估将在基线、干预后和3个月的随访中进行。结果:招募于2024年9月开始。该研究于2024年4月获得资助,第一位参与者于2024年9月入学;截至2025年3月底,共招募了132名参与者。招聘正在进行中。数据收集将于2025年7月结束,之后将开始数据分析并于2025年8月完成,主要调查结果将于2026年春季公布。结论:本研究评估了OkeyMind的有效性和成本效益,这是一个基于移动的心理教育项目,用于减少青少年的社交焦虑症状。OkeyMind可能是对抗社交焦虑的一种有希望的策略,尤其是在医疗资源有限的中低收入国家。如果有效,这种干预措施可以提供一种易于获得的、具有成本效益的方法来管理社交焦虑,特别是在资源有限的环境中。试验注册:ClinicalTrials.gov NCT06490315;https://clinicaltrials.gov/study/NCT06490315.International注册报表标识符(irrid): PRR1-10.2196/64518。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effectiveness and Cost-Effectiveness of a Mobile Psychoeducation Program (OkeyMind) for Social Anxiety Symptoms Among Youths: Protocol for a Randomized Controlled Trial.

Background: Social anxiety is increasingly prevalent among youths, leading to social withdrawal, isolation, and heightened depression risk. Mobile health (mHealth) interventions offer anonymity, accessibility, and personalized support, but their effectiveness and cost-effectiveness for young individuals with social anxiety remain unclear.

Objective: This randomized controlled trial aims to evaluate the effectiveness and cost-effectiveness of a mobile-based psychoeducation program (OkeyMind) for mitigating social anxiety symptoms among youth.

Methods: Participants aged 15 years through 24 years with mild or more severe social phobia (Social Phobia Inventory [SPIN] ≥25) and access to WeChat will be recruited and screened onsite and then randomly assigned to the intervention or waiting list control group. The study will recruit 180 participants, with 90 in each group. The intervention group will receive a 1-month mobile psychoeducation program (OkeyMind), which includes both psychoeducation and meditation components, with all content fully automated. The waiting list control group will receive the same intervention after 3 months. The primary outcome is social anxiety symptoms measured using SPIN. Secondary outcomes include depression (Patient Health Questionnaire-9) and health-related quality of life (EuroQol-5). Assessments will be conducted at baseline, postintervention, and a 3-month follow-up.

Results: Recruitment began in September 2024. The study was funded in April 2024, and the first participant was enrolled in September 2024; as of the end of March 2025, 132 participants had been recruited. Recruitment is ongoing. Data collection will conclude in July 2025, after which data analysis will begin and be completed in August 2025, with primary findings targeted for publication in spring 2026.

Conclusions: This research evaluates the effectiveness and cost-effectiveness of OkeyMind, a mobile-based psychoeducation program, for reducing social anxiety symptoms among youth. OkeyMind might be a promising strategy for combating social anxiety, especially in low- and middle-income countries with limited medical resources. If effective, this intervention could provide an accessible, cost-effective approach to managing social anxiety, particularly in resource-limited settings.

Trial registration: ClinicalTrials.gov NCT06490315; https://clinicaltrials.gov/study/NCT06490315.

International registered report identifier (irrid): PRR1-10.2196/64518.

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来源期刊
CiteScore
2.40
自引率
5.90%
发文量
414
审稿时长
12 weeks
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