心理学
发展心理学
认知
家长培训
临床心理学
干预(咨询)
精神科
作者
Georgette E. Fleming,Vilas Sawrikar,Silvana Kaouar,Bryan Neo,Campbell McDonogh,Eva R. Kimonis
标识
DOI:10.1016/j.beth.2025.02.004
摘要
• Parental cognitions predicted outcomes of Parent-Child Interaction Therapy (PCIT) • Mothers’ unhelpful cognitions predicted less improvement from baseline to follow-up. • Fathers’ unhelpful cognitions were associated with more severe baseline problems. • Fathers’ unhelpful cognitions predicted similar baseline to follow-up improvement. • Results inform treatment personalization efforts for child conduct problems. Despite decades of support for behavioral parent training, studies consistently comprise a proportion of families who do not experience sustained improvement in child conduct problems. Recent innovations to enhance treatment effects use predictors of treatment response to guide efforts to personalize treatment. We investigated whether baseline parental cognitions predicted response to Parent-Child Interaction Therapy (PCIT) in a sample of N =61 children ( M =4.78 years, SD =1.23, 74% boys) with conduct problems. Families received PCIT at an urban university-based clinic. Parental positive and negative relational schemas were coded from baseline five-minute speech samples. Linear mixed-effects models showed that mothers’ unhelpful cognitions predicted significantly less improvement in child conduct problems and internalizing problems, parenting stress, and observed parenting behaviors from baseline to follow-up. In contrast, children of fathers with unhelpful cognitions began treatment with more severe problems than other children, but experienced similar or greater magnitude of improvement in child conduct problems, paternal parenting stress, and observed paternal negative parenting behaviors during treatment relative to other children. Findings suggest that PCIT may be a useful alternative to parent-only behavioral parent training for fathers with unhelpful cognitions. We also discuss methods for tailoring PCIT for mothers with unhelpful cognitions to enhance treatment effects. These trials were registered with the Australian and New Zealand Clinical Trial Registry (ACTRN12616000280404; ACTRN12616000221459).
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