Long-Term Efficacy of a Mobile Mental Wellness Program: Prospective Single-Arm Study.

IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES JMIR mHealth and uHealth Pub Date : 2024-06-27 DOI:10.2196/54634
Meaghan McCallum, Matthew Baldwin, Paige Thompson, Kelly Blessing, Maria Frisch, Annabell Ho, Matthew Cole Ainsworth, Ellen Siobhan Mitchell, Andreas Michaelides, Christine N May
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Abstract

Background: Rising rates of psychological distress (symptoms of depression, anxiety, and stress) among adults in the United States necessitate effective mental wellness interventions. Despite the prevalence of smartphone app-based programs, research on their efficacy is limited, with only 14% showing clinically validated evidence. Our study evaluates Noom Mood, a commercially available smartphone-based app that uses cognitive behavioral therapy and mindfulness-based programming. In this study, we address gaps in the existing literature by examining postintervention outcomes and the broader impact on mental wellness.

Objective: Noom Mood is a smartphone-based mental wellness program designed to be used by the general population. This prospective study evaluates the efficacy and postintervention outcomes of Noom Mood. We aim to address the rising psychological distress among adults in the United States.

Methods: A 1-arm study design was used, with participants having access to the Noom Mood program for 16 weeks (N=273). Surveys were conducted at baseline, week 4, week 8, week 12, week 16, and week 32 (16 weeks' postprogram follow-up). This study assessed a range of mental health outcomes, including anxiety symptoms, depressive symptoms, perceived stress, well-being, quality of life, coping, emotion regulation, sleep, and workplace productivity (absenteeism or presenteeism).

Results: The mean age of participants was 40.5 (SD 11.7) years. Statistically significant improvements in anxiety symptoms, depressive symptoms, and perceived stress were observed by week 4 and maintained through the 16-week intervention and the 32-week follow-up. The largest changes were observed in the first 4 weeks (29% lower, 25% lower, and 15% lower for anxiety symptoms, depressive symptoms, and perceived stress, respectively), and only small improvements were observed afterward. Reductions in clinically relevant anxiety (7-item generalized anxiety disorder scale) and depression (8-item Patient Health Questionnaire depression scale) criteria were also maintained from program initiation through the 16-week intervention and the 32-week follow-up. Work productivity also showed statistically significant results, with participants gaining 2.57 productive work days from baseline at 16 weeks, and remaining relatively stable (2.23 productive work days gained) at follow-up (32 weeks). Additionally, effects across all coping, sleep disturbance (23% lower at 32 weeks), and emotion dysregulation variables exhibited positive and significant trends at all time points (15% higher, 23% lower, and 25% higher respectively at 32 weeks).

Conclusions: This study contributes insights into the promising positive impact of Noom Mood on mental health and well-being outcomes, extending beyond the intervention phase. Though more rigorous studies are necessary to understand the mechanism of action at play, this exploratory study addresses critical gaps in the literature, highlighting the potential of smartphone-based mental wellness programs to lessen barriers to mental health support and improve diverse dimensions of well-being. Future research should explore the scalability, feasibility, and long-term adherence of such interventions across diverse populations.

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移动心理健康计划的长期功效:前瞻性单臂研究
背景:美国成年人的心理困扰(抑郁、焦虑和压力症状)发生率不断上升,因此有必要采取有效的心理健康干预措施。尽管基于智能手机应用程序的项目很普遍,但对其功效的研究却很有限,只有 14% 的项目显示出临床验证的证据。我们的研究对 Noom Mood 进行了评估,这是一款基于智能手机的商用应用程序,采用了认知行为疗法和正念程序。在这项研究中,我们通过考察干预后的结果以及对心理健康的广泛影响,填补了现有文献的空白:Noom Mood 是一款基于智能手机的心理健康程序,旨在供普通人群使用。这项前瞻性研究评估了 Noom Mood 的疗效和干预后的结果。我们的目标是解决美国成年人日益严重的心理困扰:研究采用单臂研究设计,参与者可参加为期 16 周的 Noom Mood 计划(N=273)。分别在基线、第 4 周、第 8 周、第 12 周、第 16 周和第 32 周(16 周计划后随访)进行调查。这项研究对一系列心理健康结果进行了评估,包括焦虑症状、抑郁症状、感知压力、幸福感、生活质量、应对能力、情绪调节、睡眠和工作效率(旷工或缺勤):参与者的平均年龄为 40.5(标准差 11.7)岁。第 4 周时,焦虑症状、抑郁症状和感知压力均有明显改善,并在 16 周的干预和 32 周的随访中保持不变。前四周的变化最大(焦虑症状、抑郁症状和压力感分别降低了 29%、25% 和 15%),之后仅有小幅改善。临床相关焦虑(7 项广泛性焦虑症量表)和抑郁(8 项患者健康问卷抑郁量表)标准的降低也从项目启动到 16 周的干预和 32 周的随访期间保持不变。工作效率也取得了显著的统计结果,在 16 周时,参与者的工作效率比基线提高了 2.57 天,在 32 周的随访中,工作效率保持相对稳定(提高了 2.23 天)。此外,所有应对、睡眠障碍(32 周时降低 23%)和情绪失调变量的效果在所有时间点都呈现出积极和显著的趋势(32 周时分别提高 15%、降低 23% 和提高 25%):这项研究有助于深入了解 Noom Mood 对心理健康和幸福结果的积极影响,这种影响有望延伸到干预阶段之后。虽然要了解其作用机制还需要更严格的研究,但这项探索性研究填补了文献中的重要空白,凸显了基于智能手机的心理健康项目在减少心理健康支持障碍和改善不同幸福感方面的潜力。未来的研究应探索此类干预措施在不同人群中的可扩展性、可行性和长期坚持性。
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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.
期刊最新文献
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