Department of Computer Science, Faculty of Engineering and Vocational, Universitas Pendidikan Ganesha, Singaraja, Indonesia.
Faculty of Education, Universitas Pendidikan Ganesha, Singaraja, Bali, Indonesia.
JMIR Res Protoc. 2024 Oct 23;13:e56693. doi: 10.2196/56693.
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.
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.
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.
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.
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.
Chinese Clinical Trial Registry ChiCTR2300068085; https://tinyurl.com/2d2x4bxk.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/56693.
COVID-19 大流行增加了印度尼西亚高中教师的焦虑水平,他们在工作时间面临治疗精神障碍症状的挑战,因为印度尼西亚的心理健康服务有限。因此,为印度尼西亚的学校教师配备易于获得、私密且负担得起的早期干预措施至关重要,一种可行的方法是部署智能手机移动应用程序。
本研究的目的是(1)评估一种简短的基于正念的移动应用程序(BM-MA)在治疗焦虑和压力的印度尼西亚高中教师中的可行性,以及(2)研究使用 BM-MA 对焦虑、压力、生活满意度、自我效能感、特质正念、自我同情、身体和社交功能障碍的影响。
我们遵循 SPIRIT(推荐干预试验的标准协议项目)2013 年声明制定了本可行性随机对照试验(RCT)方案。共有 60 名印度尼西亚高中教师参与了这项研究,并按照 1:1 的比例随机分配到干预组(BM-MA)或等待名单对照组(CG)。BM-MA 组要求每天使用应用程序进行 10-20 分钟的正念练习,持续 3 周。所有参与者在基线、干预后和 1 个月随访时都使用一套自我报告量表进行评估。使用经过验证的量表来测量感兴趣的结果变量,包括生活满意度量表(SLS)、教师效能感量表(TSES)、自我同情量表-短表(SCS-SF)、广泛性焦虑障碍 7 项量表(GAD-7)、一般健康问卷 12 项量表(GHQ-12)和五因素正念量表(FFMQ)。使用客户满意度问卷 8(CSQ-8)和结构化定性访谈评估应用程序的实用性和可接受性。将使用演绎主题分析框架分析访谈数据,作为定性探究的过程。使用重复测量方差分析,以组(干预与对照)为被试间因素,时间为被试内因素(基线、干预后和 1 个月随访),检验 BM-MA 对结果变量的影响。将采用意向治疗分析方法进行数据分析,并按照 CONSORT(临床试验报告标准)建议进行报告。
参与者于 2023 年 12 月招募,本试点 RCT 于 2024 年 1 月至 3 月进行。数据分析于 2024 年 3 月至 5 月进行。预计研究结果将于 2024 年 12 月公布。该方案的试验注册已提交至中国临床试验注册中心。
本研究旨在确定基于正念的移动应用程序(BM-MA)的可行性和疗效,该应用程序是使用现有的基于正念的应用程序开发的,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。
国际注册报告标识符(IRRID):DERR1-10.2196/56693。