The more, the merrier? Establishing a dose-response relationship for the effects of cognitive control training on depressive symptomatology.

IF 4.5 1区 心理学 Q1 PSYCHOLOGY, CLINICAL Journal of consulting and clinical psychology Pub Date : 2025-03-01 DOI:10.1037/ccp0000945
Yannick Vander Zwalmen, David Demeester, Kristof Hoorelbeke, Nick Verhaeghe, Chris Baeken, Ernst H W Koster
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Abstract

Objective: Cognitive control impairments are frequently observed after remission from depression. There is evidence to show that cognitive control training (CCT) can reduce such impairments and related risk for recurrent episodes. However, it is currently unclear how many CCT sessions are required for short- and long-term effects. Method: This randomized controlled trial investigates the dose-response relationship of CCT in a sample of individuals with remitted depression (n = 216). Participants were randomly assigned to one of six arms, each receiving a different amount of training sessions (zero, one, five, 10, 15, or 20 sessions) over the course of 4 weeks, with each session lasting 15 min. Depressive symptoms and other cognitive and emotional transfer effects were examined shortly after training, as well as at 3- and 6-month follow-up. Results: We found task-specific, but no near cognitive transfer. Mixed-effects models showed that a minimum of 10 training sessions was required for a significant decrease in depressive symptoms shortly after training with medium effect sizes, but this was not maintained at 3- or 6-month follow-up. We observed reductions in perseverative thinking in all groups receiving 10 or more CCT sessions, which remained present until 6-month follow-up. Conclusions: A minimum of 10 CCT sessions is required for beneficial effects on depressive symptoms and perseverative thinking. Where perseverative thinking remained decreased long-term, this was not the case for depressive symptoms, indicating the need for continued training or the use of booster sessions to maintain training-related improvement. (PsycInfo Database Record (c) 2025 APA, all rights reserved).

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目的抑郁症缓解后经常会出现认知控制障碍。有证据表明,认知控制训练(CCT)可以减少这种障碍和相关的复发风险。然而,目前尚不清楚需要进行多少次认知控制训练才能达到短期和长期效果。方法:这项随机对照试验以抑郁症缓解患者(n = 216)为样本,研究了 CCT 的剂量-反应关系。参与者被随机分配到六组中的一组,每组在 4 周内接受不同次数的训练(0、1、5、10、15 或 20 次),每次训练持续 15 分钟。在训练后不久,以及3个月和6个月的随访中,对抑郁症状和其他认知及情绪转移效应进行了检测。结果:我们发现了针对特定任务的认知迁移,但没有发现近似的认知迁移。混合效应模型显示,至少需要进行 10 次训练,才能在训练后不久显著减少抑郁症状,并达到中等效应大小,但在 3 个月或 6 个月的随访中,这种效应并没有得到维持。我们观察到,在接受 10 次或更多 CCT 训练的所有小组中,顽固性思维都有所减少,这种情况一直持续到 6 个月的随访。结论:至少接受 10 次 CCT 治疗才能对抑郁症状和顽固性思维产生有益影响。在持久性思维长期保持下降的情况下,抑郁症状却并非如此,这表明需要继续训练或使用强化课程来保持与训练相关的改善。(PsycInfo Database Record (c) 2025 APA, 版权所有)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.00
自引率
3.40%
发文量
94
期刊介绍: The Journal of Consulting and Clinical Psychology® (JCCP) publishes original contributions on the following topics: the development, validity, and use of techniques of diagnosis and treatment of disordered behaviorstudies of a variety of populations that have clinical interest, including but not limited to medical patients, ethnic minorities, persons with serious mental illness, and community samplesstudies that have a cross-cultural or demographic focus and are of interest for treating behavior disordersstudies of personality and of its assessment and development where these have a clear bearing on problems of clinical dysfunction and treatmentstudies of gender, ethnicity, or sexual orientation that have a clear bearing on diagnosis, assessment, and treatmentstudies of psychosocial aspects of health behaviors. Studies that focus on populations that fall anywhere within the lifespan are considered. JCCP welcomes submissions on treatment and prevention in all areas of clinical and clinical–health psychology and especially on topics that appeal to a broad clinical–scientist and practitioner audience. JCCP encourages the submission of theory–based interventions, studies that investigate mechanisms of change, and studies of the effectiveness of treatments in real-world settings. JCCP recommends that authors of clinical trials pre-register their studies with an appropriate clinical trial registry (e.g., ClinicalTrials.gov, ClinicalTrialsRegister.eu) though both registered and unregistered trials will continue to be considered at this time.
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