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在线心理教育与放松训练项目(OnPR)对新冠肺炎患者心理健康问题的疗效:一项随机对照试验。

Efficacy of online psychoeducation and relaxation training program (OnPR) on mental health problems in COVID-19 patients: A randomized controlled trial.

作者信息

Chinvararak Chotiman, Kirdchok Pantri, Wonglertwisawakorn Chayut, Pumjun Pachara, Kerdcharoen Nitchawan

机构信息

Department of Psychiatry, Faculty of Medicine Vajira Hospital, Navamindradhiraj University, Bangkok, Thailand.

Department of Urban Medicine, Faculty of Medicine Vajira Hospital, Navamindradhiraj University, Bangkok, Thailand.

出版信息

Internet Interv. 2024 Jan 5;35:100705. doi: 10.1016/j.invent.2023.100705. eCollection 2024 Mar.

Abstract

PURPOSE

Prior studies found that the prevalence of anxiety, depression, stress and insomnia were relatively high in COVID-19 patients. This study aimed to explore the efficacy of OnPR on mental health outcomes in patients with asymptomatic or mildly symptomatic COVID-19.

PATIENTS AND METHODS

We employed a randomized controlled trial following the CONSORT guidelines. The Thai Clinical Trials Registry identification number of this study is TCTR20220729003. We used a block of 4 randomizations generated by a computer program. The intervention group (n = 38) received the OnPR program, and the control group (n = 36) received care as usual. OnPR was an online psychological intervention comprising psychoeducation, sleep hygiene education and relaxation techniques. OnPR was provided by qualified therapists trained with a standard protocol. The primary outcomes were depression, anxiety, and stress, which were determined by the Depression Anxiety and Stress Scale-21 (DASS-21). Sleep quality was measured by the Pittsburgh Sleep Quality Index (PSQI). Outcomes were compared between groups at pre-intervention and post-intervention at 1, 4, and 12 weeks using paired -test or Wilcoxon signed-rank test. In addition, a linear mixed model was employed to demonstrate the effect changes of OnPR over time. All analyses were two-tailed, with a significance level of 0.05.

RESULTS

Of 74 Thai participants, 89.2 % were female, and 11.8 % were male. The average age was 31 years. Participants' baseline characteristics were not statistically significant between the intervention and control groups except for depression and stress scores from DASS-21. OnPR resulted in significantly better improvement in depression, anxiety, stress, and sleep quality. The mean differences between groups of DASS-21 scores in depression, anxiety and stress at 7-day follow-up were -4.69, -3.29, and -5.50 respectively. The differences continue to be significant at 4-week and 12-week follow-ups. The mean difference between groups of PSQI at 7-day follow-up is -0.91.

CONCLUSION

OnPR improved mental health outcomes, and the effect on depression, anxiety and stress lasted for at least a 12-week follow-up period. In addition, it could enhance sleep quality after the intervention.

摘要

目的

先前的研究发现,新冠病毒肺炎(COVID-19)患者中焦虑、抑郁、压力和失眠的患病率相对较高。本研究旨在探讨在线个性化心理康复(OnPR)对无症状或轻症COVID-19患者心理健康结局的疗效。

患者与方法

我们采用了一项遵循CONSORT指南的随机对照试验。本研究在泰国临床试验注册中心的识别号为TCTR20220729003。我们使用计算机程序生成的4个随机分组块。干预组(n = 38)接受OnPR项目,对照组(n = 36)接受常规护理。OnPR是一种在线心理干预,包括心理教育、睡眠卫生教育和放松技巧。OnPR由接受标准方案培训的合格治疗师提供。主要结局为抑郁、焦虑和压力,通过抑郁焦虑压力量表-21(DASS-21)进行测定。睡眠质量通过匹兹堡睡眠质量指数(PSQI)进行测量。在干预前以及干预后1周、4周和12周,使用配对t检验或Wilcoxon符号秩检验对两组的结局进行比较。此外,采用线性混合模型来证明OnPR随时间的效果变化。所有分析均为双侧检验,显著性水平为0.05。

结果

在74名泰国参与者中,89.2%为女性,11.8%为男性。平均年龄为31岁。除了DASS-21的抑郁和压力评分外,干预组和对照组参与者的基线特征在统计学上无显著差异。OnPR在抑郁、焦虑、压力和睡眠质量方面带来了显著更好的改善。在7天随访时,两组DASS-21抑郁、焦虑和压力评分的组间平均差异分别为-4.69、-3.29和-5.50。在4周和12周随访时,差异仍然显著。在7天随访时,两组PSQI的组间平均差异为-0.91。

结论

OnPR改善了心理健康结局,对抑郁、焦虑和压力的影响在至少12周的随访期内持续存在。此外,它在干预后可以提高睡眠质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96ac/10808897/f8470b59f1f4/gr1.jpg

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