创伤后功能障碍认知的改变对PTSD症状群的预测有差异吗?

IF 4.5 1区 心理学 Q1 PSYCHOLOGY, CLINICAL
Hannah Schumm, Antje Krüger-Gottschalk, Thomas Ehring, Anne Dyer, Andre Pittig, Keisuke Takano, Georg W Alpers, Barbara Cludius
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引用次数: 0

摘要

目的:近年来,创伤后功能障碍认知的改变被认为是创伤后应激障碍(PTSD)认知行为治疗(CBT)改变的重要机制。事实上,一些研究表明,创伤后功能失调认知的变化先于并预测了症状的变化。然而,这些研究已经调查了对整体症状严重程度的影响-尽管众所周知的创伤后应激障碍的多维性。因此,本研究旨在探讨功能障碍状况变化与PTSD症状群变化之间的差异关联。方法:作为评估创伤性认知行为疗法在常规临床护理中的有效性研究的一部分,61例创伤后应激障碍患者在治疗过程中每5次填写创伤后功能障碍认知和PTSD症状严重程度的测量。在接下来的时间点,使用线性混合模型检查功能障碍认知和症状严重程度之间的滞后关联。结果:在治疗过程中,认知功能障碍和PTSD症状均有所减轻。创伤后认知预测了随后的创伤后应激障碍症状的严重程度,尽管这种影响至少部分是由时间因素解释的。此外,功能失调的认知预测了四种症状群中的三种。然而,当时间的一般效应受到控制时,这些效应不再具有统计学意义。结论:本研究为创伤后认知功能障碍对PTSD症状群的预测提供了初步证据。然而,当采用传统方法和更严格的统计方法时,不同的发现使得解释发现变得困难。(PsycInfo数据库记录(c) 2023 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。
Do changes in dysfunctional posttraumatic cognitions differentially predict PTSD symptom clusters?

Objective: In recent years, it has been suggested that the modification of dysfunctional posttraumatic cognitions plays a central role as a mechanism of change in cognitive behavioral therapy (CBT) for posttraumatic stress disorder (PTSD). Indeed, several studies have shown that changes in dysfunctional posttraumatic cognitions precede and predict symptom change. However, these studies have investigated the influence on overall symptom severity-despite the well-known multidimensionality of PTSD. The present study therefore aimed to explore differential associations between change in dysfunctional conditions and change in PTSD symptom clusters.

Method: As part of a naturalistic effectiveness study evaluating trauma-focused cognitive behavioral therapy for PTSD in routine clinical care, 61 patients with PTSD filled out measures of dysfunctional posttraumatic cognitions and PTSD symptom severity every five sessions during the course of treatment. Lagged associations between dysfunctional cognitions and symptom severity at the following timepoint were examined using linear mixed models.

Results: Over the course of therapy, both dysfunctional cognitions and PTSD symptoms decreased. Posttraumatic cognitions predicted subsequent total PTSD symptom severity, although this effect was at least partly explained by the time factor. Moreover, dysfunctional cognitions predicted three out of four symptom clusters as expected. However, these effects were no longer statistically significant when the general effect for time was controlled for.

Conclusion: The present study provides preliminary evidence that dysfunctional posttraumatic cognitions predict PTSD symptom clusters differentially. However, different findings when employing a traditional versus a more rigorous statistical approach make interpretation of findings difficult. (PsycInfo Database Record (c) 2023 APA, all rights reserved).

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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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