创伤后应激障碍长期暴露和以现状为中心的治疗的治疗时间和症状改善:比较两种手动干预的剂量反应和足够好的水平模型。

IF 4.5 1区 心理学 Q1 PSYCHOLOGY, CLINICAL Journal of consulting and clinical psychology Pub Date : 2023-10-01 Epub Date: 2023-07-20 DOI:10.1037/ccp0000834
Johanna Thompson-Hollands, Carole A Lunney, Denise M Sloan, Shannon Wiltsey Stirman, Paula P Schnurr
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引用次数: 0

摘要

目的:心理治疗变化的剂量反应模型认为,每一次治疗对患者都是递增的有益。对比良好水平模型表明,患者在治疗中的改善率不同,当他们对自己的改善感到满意时,停止治疗。对每种理论的支持都参差不齐,许多先前的研究都依赖于接受非结构化治疗方法的患者样本。我们进行了这项研究,以比较创伤后应激障碍(PTSD)的两种手动治疗方法中的这两种理论,或以当前为中心的治疗(PCT),一种非创伤为主的治疗。参与者在偶数次治疗中完成了创伤后应激障碍检查表(PCL),并监测了辍学/治疗完成的时间。结果:不同治疗的辍学最高风险点不同,PE的风险与想象暴露的开始相对应。在PE条件下,但在PCT条件下,完成的疗程数量越高,实现可靠的临床显著改善的可能性就越大。在不同的治疗中,创伤后应激障碍症状的变化率根据完成的疗程数没有差异(b=0.06,p=.687)。结论:研究结果支持心理治疗变化的剂量反应模型。不同治疗条件下的辍学率存在显著差异,包括发病率、时间和对结果的影响。这些差异可能反映了协议之间内容的差异。(PsycInfo数据库记录(c)2023 APA,保留所有权利)。
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Treatment length and symptom improvement in prolonged exposure and present-centered therapy for posttraumatic stress disorder: Comparing dose-response and good-enough level models in two manualized interventions.

Objective: The dose-response model of change in psychotherapy posits that each session of therapy is incrementally beneficial across patients. The contrasting good-enough level model suggests that patients improve at different rates in therapy and discontinue treatment when they are satisfied with their improvement. Support for each theory has been mixed, and many prior studies have relied on samples of patients receiving unstructured treatment approaches. We conducted this study to compare these two theories across two manualized treatments for posttraumatic stress disorder (PTSD).

Method: Two hundred eighty-four female veterans and military service members with PTSD (Mage = 44.79; 54.6% White non-Hispanic, 6.7% Black non-Hispanic, 37% other) were randomized to receive 10 sessions of prolonged exposure (PE), a trauma-focused therapy, or present-centered therapy (PCT), a non-trauma-focused therapy. Participants completed the PTSD Checklist (PCL) at even-numbered treatment sessions, and the timing of dropout/treatment completion was monitored.

Results: The point of highest risk for dropout differed between the treatments, with risk in PE corresponding to the beginning of imaginal exposures. In the PE condition, but not in PCT, a higher number of sessions completed increased the likelihood of achieving reliable clinically significant improvement. Across treatments, the rate of change in PTSD symptoms did not differ according to the number of sessions completed (b = 0.06, p = .687).

Conclusions: Findings support the dose-response model of change in psychotherapy. There were notable differences in dropout across the treatment conditions, including rates, timing, and implications for outcomes. These differences likely reflect differences in content between the protocols. (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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