针对印度尼西亚高中教师的基于移动应用程序的简短正念干预:随机对照试验方案》。

IF 1.4 Q3 HEALTH CARE SCIENCES & SERVICES
Gede Rasben Dantes, Nice Maylani Asril, Andrian Liem, Ni Komang Arie Suwastini, Shian-Ling Keng, Ni Wayan Surya Mahayanti
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引用次数: 0

摘要

背景:COVID-19 的流行加剧了印尼高中教师的焦虑程度,由于印尼的心理健康服务有限,他们在治疗工作时间出现的精神障碍症状方面面临挑战。因此,为印尼的学校教师提供易于获得、私密且经济实惠的早期干预措施至关重要,而部署智能手机移动应用程序就是一种可行的方法:本研究的目的是:(1)评估基于正念的简短移动应用程序(BM-MA)对经历焦虑和压力的印度尼西亚高中教师的可行性;(2)研究使用 BM-MA 对参与者的焦虑、压力、生活满意度、自我效能感、正念特质、自我同情以及身体和社会功能障碍的影响:我们按照2013年SPIRIT(标准协议项目:干预性试验建议)声明制定了这项可行性随机对照试验(RCT)方案。本研究共招募了 60 名印度尼西亚高中教师,并按 1:1 的比例随机分配到干预组(BM-MA)或等待对照组(CG)。BM-MA组需要在3周内每天使用应用程序进行10-20分钟的正念练习。所有参与者在基线、干预后和 1 个月随访时都接受了一系列自我报告评估。用于测量相关结果变量的经过验证的量表包括:生活满意度量表(SLS)、教师效能感量表(TSES)、自我同情量表-简表(SCS-SF)、广泛性焦虑症-7(GAD-7)、一般健康问卷-12(GHQ-12)和五方面正念问卷(FFMQ)。该应用程序的实用性和可接受性将通过客户满意度问卷-8(CSQ-8)和结构化定性访谈进行评估。访谈数据将采用演绎主题分析框架进行分析,作为定性调查的一个过程。将使用重复测量方差分析,以组别(干预与对照)作为主体间因素,时间作为主体内因素(基线、干预后和 1 个月的随访),来研究 BM-MA 对结果变量的影响。数据将采用意向治疗法进行分析,并根据 CONSORT(试验报告统一标准)的建议进行公布:2023 年 12 月开始招募参与者,2024 年 1 月至 3 月开展了这项试验性 RCT。数据分析于 2024 年 3 月至 5 月进行。研究结果预计将于 2024 年 12 月公布。本方案的试验注册已提交至中国临床试验注册中心:本研究旨在确定BM-MA的可行性和有效性,BM-MA是利用现有的正念应用程序开发的一种数字心理健康干预方法,并评估其广泛应用的潜力:中国临床试验注册中心ChiCTR2300068085;https://tinyurl.com/2d2x4bxk.International 注册报告标识符(irrid):DERR1-10.2196/56693。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Brief Mobile App-Based Mindfulness Intervention for Indonesian Senior High School Teachers: Protocol for a Pilot Randomized Controlled Trial.

Background: The COVID-19 pandemic has increased the level of anxiety among Indonesian senior high school teachers, who face challenges to treat their mental disorder symptoms that arise during their working hours, as mental health services in Indonesia are limited. Therefore, it is vital to equip schoolteachers in Indonesia with early interventions that are easily available, private, and affordable, and 1 feasible approach is to deploy a smartphone mobile app.

Objective: The objectives of this study are (1) to evaluate the feasibility of a brief mindfulness-based mobile app (BM-MA) for Indonesian senior high school teachers experiencing anxiety and stress and (2) to examine the effects of using the BM-MA on anxiety, stress, life satisfaction, self-efficacy, trait mindfulness, self-compassion, and physical and social dysfunction among the participants.

Methods: We followed the SPIRIT (Standard Protocol Items: Recommendations for Interventional Trials) 2013 statement for this feasibility randomized controlled trial (RCT) protocol. A total of 60 Indonesian senior high school teachers were recruited for this study and randomly assigned to either the intervention group (BM-MA) or a wait-list control group (CG) in a 1:1 ratio. The BM-MA group was required to engage in mindfulness practices using the app for 10-20 minutes per day for 3 weeks. All participants were assessed with a battery of self-report measures at baseline, postintervention, and at 1-month follow-up. Validated scales used to measure the outcome variables of interest included the Satisfaction With Life Scale (SLS), the Teachers' Sense of Efficacy Scale (TSES), the Self-Compassion Scale-Short Form (SCS-SF), Generalized Anxiety Disorder-7 (GAD-7), General Health Questionnaire-12 (GHQ-12), and the Five Facet Mindfulness Questionnaire (FFMQ). The practicality and acceptability of the app will be evaluated using the Client Satisfaction Questionnaire-8 (CSQ-8) and structured qualitative interviews. Data from the interviews will be analyzed with the deductive thematic analysis framework as a process of qualitative inquiry. Repeated measures ANOVA with groups (intervention vs control) as a between-subject factor and time as a within-subject factor (baseline, postintervention, and 1-month follow-up) will be used to examine the effects of the BM-MA on the outcome variables. The data will be analyzed using an intent-to-treat approach and published in accordance with CONSORT (Consolidated Standards of Reporting Trials) recommendations.

Results: Participants were recruited in December 2023, and this pilot RCT was conducted from January through March 2024. Data analysis was conducted from March through May 2024. The results of this study are expected to be published in December 2024. The trial registration of this protocol was submitted to the Chinese Clinical Trial Registry.

Conclusions: This study aims to determine the feasibility and efficacy of the BM-MA, a digital mental health intervention developed using an existing mindfulness-based app, and assess its potential for widespread use.

Trial registration: Chinese Clinical Trial Registry ChiCTR2300068085; https://tinyurl.com/2d2x4bxk.

International registered report identifier (irrid): DERR1-10.2196/56693.

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来源期刊
CiteScore
2.40
自引率
5.90%
发文量
414
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