对晚期癌症患者进行心理干预的可行性和益处的性别敏感分析

G. Shapiro, K. Mah, F. D. de Vries, C. Zimmermann, Madeline Li, S. Hales, G. Rodin
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引用次数: 0

摘要

文本中提供了补充数字内容。背景:性别在心理治疗中的作用已被广泛认可,但在心理治疗试验中很少进行研究。我们对癌症管理和有意义生活(CALM)随机对照试验的数据进行了二次分析,以检查性别对CALM的可行性、可接受性、感知效益和有效性的影响。方法:试验参与者,晚期癌症门诊患者(N=305,40%男性和60%女性),在基线、3个月(t1)和6个月(t2)完成测量。我们调查了参与率、自然减员率、接受CALM治疗的次数和CALM的感知益处方面的性别差异。在检查每个随访期对抑郁症状、临终准备和死亡焦虑的治疗效果时,对来自男性和女性的数据的单独亚组分析和性别×治疗组调节因素分析进行了比较。结果:在参与率或自然减员率、接受CALM治疗的次数或CALM的感知益处方面没有观察到性别差异。在t2的亚组分析中,CALM中的男性报告的抑郁症状明显低于常规护理中的男性(UC;P=.017),具有中度基线死亡焦虑的CALM中女性报告的死亡焦虑低于UC中的女性(P=.009),CALM的男性(P=.022)和女性(P=.016)报告的临终准备均高于UC。性别×治疗组交互作用对任何结果均无显著影响。结论:CALM治疗是可行的,可接受的,对男性和女性的不同结果有益。需要对性别认同进行进一步的临床试验,以评估晚期疾病患者心理治疗干预中的性别影响。
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A gender-sensitive analysis of the feasibility and benefit of a psychological intervention for patients with advanced cancer
Supplemental Digital Content is Available in the Text. Background: The role of gender in psychotherapy has been widely recognized but infrequently investigated in psychotherapy trials. We conducted a secondary analysis of data from a randomized controlled trial of Managing Cancer and Living Meaningfully (CALM), a supportive-expressive intervention for individuals with advanced cancer, to examine gender effects in the feasibility, acceptability, perceived benefit, and effectiveness of CALM. Methods: Trial participants, outpatients with advanced cancer (N = 305, 40% men and 60% women), completed measures at baseline, 3 months (t1), and 6 months (t2). We investigated gender differences in participation rates, attrition rates, number of CALM sessions received, and perceived benefit of CALM. Separate subgroup analyses of data and gender × treatment group moderator analyses from men and women were compared in examining treatment effects on depressive symptoms, end-of-life preparation, and death anxiety at each follow-up period. Results: No gender differences were observed in participation or attrition rates, number of CALM sessions received, or perceived benefit of CALM. In subgroup analyses at t2, men in CALM reported significantly lower depressive symptoms than men in usual care (UC; P = .017), women in CALM with moderate baseline death anxiety reported lower death anxiety than women in UC (P = .009), and both men (P = .022) and women (P = .016) in CALM reported greater end-of-life preparation than those in UC. There were no significant gender × treatment group interaction effects on any outcome. Conclusions: CALM therapy is feasible, acceptable, and beneficial on different outcomes for men and women. Further clinical trials with comprehensive measures of gender identity are needed to evaluate gender effects in psychotherapeutic interventions for patients with advanced disease.
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