基于cerina -认知行为疗法的移动应用程序管理大学生广泛性焦虑障碍症状:来自一项试点可行性随机对照试验的结果。

IF 6.2 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Ozlem Eylem-van Bergeijk, Tony Robinson, Matthew Manktelow, Michail Olympios, Siobhan Poulter, Prasannajeet Mane, Maria Panagioti, Joan Condell, Gerard Leavey
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引用次数: 0

摘要

背景:广泛性焦虑障碍(GAD)在大学生中很常见,因为学业压力和经济不确定性以及其他挑战。尽管有这种需要,但现有心理服务的接受率往往很低。目的:本研究探讨了基于数字无指导认知行为疗法(CBT)的移动应用程序Cerina的可行性,并与等待列表对照组相比,研究了这种干预在减轻广泛性焦虑症症状方面的可能效果。方法:通过网络问卷对有轻度至中度广泛性焦虑症症状的符合条件的学生(n=158)进行自我评估,并根据知情同意随机分配到干预组(n=79)或等候名单对照组(n=79)。干预组直接使用Cerina,并进行为期6周的基于cbt的互动会话。等候名单控制组的参与者可以获得可选的校园福利服务,并在随机分组后6周获得Cerina。参与者在三个时间点完成了焦虑、抑郁、担忧和可用性的评估。此外,在完成干预后,他们被邀请参加一个基于网络的访谈,以更深入地了解干预的实施情况。结果:平均13%(10/79)的干预组参与者退出,61%(36/69)的干预组参与者完成了核心临床内容(2次),12%(7/69)的干预组参与者完成了预期的治疗次数(6或7次)。对完成者(2个或更多疗程)的分析显示,干预组在GAD(平均8.4,SD 3.7; t42=-2.25; P= 0.03; d=-0.7)和焦虑症状(平均42.3,SD 10.8; t42=-2.50; P= 0.02; d=-0.8)以及功能障碍(平均16.7,SD 2.44; t42=-2.12; P= 0.04; d=-0.6)方面具有显著的组间差异,后测效果中至大。意向治疗分析证实GAD组间差异显著(平均8.47,SD 2.7; t156=-2.23; P=.03; d=-0.4),焦虑症状组间差异不显著(平均41.5,SD 8.40; t156=-1.94; P=.05; d=-0.3),后测效果中等,有利于干预组。这些结果表明,干预对减轻GAD症状有意义的影响,对减轻参与者的担忧症状有适度的影响。结论:Cerina应用程序在减轻学生GAD症状方面显示出令人鼓舞的效果。这一结果支持了其他随机对照试验的发现,表明基于数字cbt的干预措施对出现广泛性焦虑症症状的广泛年龄组和人群是有效和可行的。完成推荐会话数的参与者数量较少表明存在可用性问题。为了解决这个问题,可以通过用户反馈的迭代设计过程来改进干预措施,并且可以通过扩展评估来评估特定粘性功能在提高可用性和留存率方面的长期影响。试验注册:ClinicalTrials.gov NCT06146530;https://clinicaltrials.gov/study/NCT06146530.International注册报告标识符(irrid): RR2-10.1136/bmjopen-2023-083554。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cerina-Cognitive Behavioral Therapy-Based Mobile App for Managing Generalized Anxiety Disorder Symptoms Among University Students: Results From a Pilot Feasibility Randomized Controlled Trial.

Background: Generalized anxiety disorder (GAD) is common among university students due to academic pressure and financial uncertainty, among other challenges. Despite the need, the receipt of available psychological services is often low.

Objective: This study investigates the feasibility of a digital unguided cognitive behavioral therapy (CBT)-based mobile app, Cerina, and examines the likely effects of this intervention in reducing GAD symptoms compared to the waitlist control group.

Methods: Eligible students (n=158) with mild to moderate GAD symptoms were self-assessed through web-based questionnaires and were randomly allocated to the intervention group (n=79) or to the waitlist control group (n=79) following their informed consent. The intervention group had direct access to Cerina and followed CBT-based interactive sessions for 6 weeks. The waitlist control group participants had access to optional on-campus well-being services, and they were given access to Cerina 6 weeks after their randomization. Participants completed assessments on anxiety, depression, worry, and usability at three time points. Additionally, upon completing the intervention, they were invited to a web-based interview to understand the implementation of the intervention in more depth.

Results: On average, 13% (10/79) intervention group participants dropped out, 61% (36/69) completed the core clinical content (2 sessions), and 12% (7/69) completed the desired number of sessions (6 or 7 sessions). Analyses of the completers (2 or more sessions) revealed significant group differences in GAD (mean 8.4, SD 3.7; t42=-2.25; P=.03; d=-0.7) and worry symptoms (mean 42.3, SD 10.8; t42=-2.50; P=.02; d=-0.8), as well as functional impairment (mean 16.7, SD 2.44; t42=-2.12; P=.04; d=-0.6) in favor of the intervention group at posttest with medium to large effect sizes. The intention-to-treat analyses confirmed significant group differences in GAD (mean 8.47, SD 2.7; t156=-2.23; P=.03; d=-0.4), and there were marginally nonsignificant group differences in worry symptoms (mean 41.5, SD 8.40; t156=-1.94; P=.05; d=-0.3) in favor of the intervention group at posttest with medium effect sizes. These results suggest that the intervention had a meaningful impact on reducing GAD symptoms and a modest impact on reducing worry symptoms among participants.

Conclusions: The Cerina app showed promising results in reducing GAD symptoms among students. This result supports findings from other randomized controlled trials showing that digital CBT-based interventions are effective and feasible for a wide range of age groups and populations experiencing GAD symptoms. The low number of participants completing the recommended number of sessions suggests a usability issue. To address this, the intervention could be refined through an iterative design process informed by user feedback, and the long-term impact of specific engagement features in improving usability and retention could be assessed through extended evaluations.

Trial registration: ClinicalTrials.gov NCT06146530; https://clinicaltrials.gov/study/NCT06146530.

International registered report identifier (irrid): RR2-10.1136/bmjopen-2023-083554.

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来源期刊
JMIR mHealth and uHealth
JMIR mHealth and uHealth Medicine-Health Informatics
CiteScore
12.60
自引率
4.00%
发文量
159
审稿时长
10 weeks
期刊介绍: JMIR mHealth and uHealth (JMU, ISSN 2291-5222) is a spin-off journal of JMIR, the leading eHealth journal (Impact Factor 2016: 5.175). JMIR mHealth and uHealth is indexed in PubMed, PubMed Central, and Science Citation Index Expanded (SCIE), and in June 2017 received a stunning inaugural Impact Factor of 4.636. The journal focusses on health and biomedical applications in mobile and tablet computing, pervasive and ubiquitous computing, wearable computing and domotics. JMIR mHealth and uHealth publishes since 2013 and was the first mhealth journal in Pubmed. It publishes even faster and has a broader scope with including papers which are more technical or more formative/developmental than what would be published in the Journal of Medical Internet Research.
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