The role of "dose" of therapy and therapy formulation level in improvements in social support appraisals and concomitant reductions in suicidal ideation severity over 6 months in people with psychosis.

IF 6 1区 心理学 Q1 PSYCHOLOGY, CLINICAL
Patricia Gooding, Daniel Pratt, Connor Heapy, Kamelia Harris, Richard J Drake, Gillian Haddock
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Abstract

Objective: The objectives were to examine the role of two therapy process variables (formulation level and therapy "dose") in a mechanism involving links between improved social support appraisals and reduced suicidal ideation severity over time in people with psychosis and to determine which aspects of social support were key to improvements in suicidal ideation.

Method: Participants (N = 106) had nonaffective psychosis and recent suicidal experiences and had received a suicide-focused talking therapy. A model was tested in which, across 6 months, changes in social support appraisals were associated with changes in suicidal ideation severity with sequential mediators of therapy "dose" (number of sessions) and therapy formulation level (1-5). Multivariate techniques were used to probe which social support items clustered around suicidal ideation improvements and the two therapy process variables.

Results: The highest levels of formulation (Levels 4 and 5) were attained by 77% of participants, with median therapy attendance of 17 sessions. Therapy "dose" and therapy formulation level acted as sequential mediators in a significant indirect pathway in which improvements to social support appraisals led to consequent improvements in suicidal ideation severity, with social support from family being key. Aspects of social connectedness of particular importance included feeling important to others, being able to rely on family, being relied upon by family, and being cared for by family.

Conclusions: People with some of the most severe mental health problems can fully engage with suicide-focused therapy. Individualized formulation is recommended which is to focus upon transitions within social connectedness appraisals. (PsycInfo Database Record (c) 2026 APA, all rights reserved).

治疗“剂量”和治疗配方水平在精神病患者6个月内改善社会支持评估和伴随的自杀意念严重程度降低中的作用
目的:目的是检查两个治疗过程变量(配方水平和治疗“剂量”)在改善社会支持评估和减少精神病患者自杀意念严重程度之间的联系机制中的作用,并确定社会支持的哪些方面是改善自杀意念的关键。方法:有非情感性精神病和近期自杀经历的参与者(106例)接受了以自杀为重点的谈话治疗。我们测试了一个模型,在6个月的时间里,社会支持评估的变化与自杀意念严重程度的变化相关,治疗“剂量”(治疗次数)和治疗配方水平(1-5)是顺序介质。采用多变量技术探讨哪些社会支持项目聚集在自杀意念改善和两个治疗过程变量周围。结果:77%的参与者达到了最高水平的配方(4级和5级),中位治疗出席率为17次。治疗“剂量”和治疗配方水平在社会支持评价改善导致自杀意念严重程度随之改善的重要间接途径中起序贯中介作用,其中来自家庭的社会支持是关键。社会联系特别重要的方面包括感觉对他人很重要,能够依靠家人,被家人依靠,被家人照顾。结论:有一些最严重的心理健康问题的人可以完全参与以自杀为重点的治疗。个性化的提法被推荐,即关注社会联系评价中的转变。(PsycInfo数据库记录(c) 2026 APA,版权所有)。
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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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