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Complaint-Directed Mini-Interventions for Depressive Complaints: A Randomized Controlled Trial of Unguided Web-Based Self-Help Interventions

机译:针对抑郁症投诉的针对投诉的小型干预措施:基于Web的无指导自助干预的随机对照试验

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Background: Prevention of depression is important due to the substantial burden of disease associated with it. To this end, we developed a novel, brief, and low-threshold Web-based self-help approach for depressive complaints called complaint-directed mini-interventions (CDMIs). These CDMIs focus on highly prevalent complaints that are demonstrably associated with depression and have a substantial economic impact: stress, sleep problems, and worry.Objective: The aim was to evaluate the effectiveness of the Web-based self-help CDMIs in a sample of adults with mild-to-moderate depressive symptoms compared to a wait-list control group.Methods: A two-armed randomized controlled trial was conducted. An open recruitment strategy was used. Participants were randomized to either the Web-based CDMIs or the no-intervention wait-list control group. The CDMIs are online, unguided, self-help interventions, largely based on cognitive behavioral techniques, which consist of 3 to 4 modules with up to 6 exercises per module. Participants are free to choose between the modules and exercises. Assessments, using self-report questionnaires, took place at baseline and at 3 and 6 months after baseline. The control group was given access to the intervention following the 3-month assessment. The primary goal of the CDMIs is to reduce depressive complaints. The primary outcome of the study was a reduction in depressive complaints as measured by the Inventory of Depressive Symptomatology Self-Report (IDS-SR). Secondary outcomes included reductions in stress, worry, sleep problems, and anxiety complaints, and improvements in well-being. Data were analyzed using linear mixed models.Results: In total, 329 participants enrolled in the trial, of which 165 were randomized to the intervention group and 164 to the control group. Approximately three-quarters of the intervention group actually created an account. Of these participants, 91.3% (116/127) logged into their chosen CDMI at least once during the 3-month intervention period (median 3, range 0-166). After 3 months, there was a significant reduction in depressive symptomatology for participants in the intervention group compared to participants in the wait-list control group (reduction in depression: mean –4.47, 95% CI –6.54 to –2.40; Cohen d=–0.70). Furthermore, significant effects were observed for sleep problems, worry, anxiety, and well-being, with effect sizes ranging from –0.29 to –0.40. The intervention did not significantly reduce stress. At 6-month follow-up, the improvements in the intervention group were generally sustained.Conclusions: This study shows that the online self-help CDMIs have a positive impact on various mental health outcomes. Future research should focus on which specific strategies may boost adherence, and increase the reach of the CDMIs among people with low socioeconomic status.ClinicalTrial: Netherlands Trial Register (NTR): NTR4612; http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=4612 (Archived by WebCite at http://www.webcitation.org/6n4PVYddM)
机译:背景:由于与抑郁症相关的巨大疾病负担,预防抑郁症很重要。为此,我们开发了一种新颖,简短且低阈值的基于Web的抑郁症自助式方法,称为投诉指导型迷你干预(CDMI)。这些CDMI专注于与抑郁症相关的高度普遍的抱怨,这些抱怨明显地与抑郁症相关,并且对经济产生重大影响:压力,睡眠问题和忧虑。目的:旨在评估基于Web的自助CDMI在以下人群中的有效性:与等待列表对照组相比,患有轻度至中度抑郁症的成年人。方法:进行了两臂随机对照试验。使用了开放的招聘策略。参与者被随机分配到基于Web的CDMI或无干预等待列表对照组。 CDMI是在线的,无向导的自助干预措施,主要基于认知行为技术,由3至4个模块组成,每个模块最多6个练习。参与者可以在模块和练习之间自由选择。使用自我报告调查表进行的评估在基线以及基线后3个月和6个月进行。在3个月的评估后,对照组获得了干预的机会。 CDMI的主要目标是减少抑郁症。该研究的主要结果是通过抑郁症症状自我报告清单(IDS-SR)测得的抑郁症状有所减少。次要结果包括减轻压力,担心,睡眠问题和焦虑症,以及改善健康状况。结果:共有329名参与者参加了该试验,其中165名被随机分配到干预组,而164名被随机分配到对照组。干预小组中大约四分之三实际上创建了一个帐户。在这些参与者中,有91.3%(116/127)在3个月的干预期内至少登录过一次他们选择的CDMI(中位数3,范围0-166)。 3个月后,干预组参与者的抑郁症状与等待列表对照组相比显着减少(抑郁症的减少:平均–4.47,95%CI –6.54至–2.40; Cohen d = – 0.70)。此外,在睡眠问题,忧虑,焦虑和福祉方面也观察到了显着的影响,影响范围为–0.29至–0.40。干预并未显着减轻压力。在6个月的随访中,干预组的改善总体上得以维持。结论:本研究表明,在线自助CDMI对各种心理健康结局具有积极影响。未来的研究应集中于哪些特定策略可以提高依从性,并增加低社会经济地位人群中CDMI的覆盖范围。临床试验:荷兰试验注册(NTR):NTR4612; http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=4612(由WebCite存档,网址为http://www.webcitation.org/6n4PVYddM)

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