随机临床试验:以小组为基础的接受与承诺治疗计划对高度恐惧病情恶化的乳腺癌患者的疗效。

Psycho-Oncology Pub Date : 2024-04-01 DOI:10.1002/pon.6339
Fatemeh Hassani Alimolk, F. McDonald, Mohammad Asghari-Jafarabadi, F. Ahmadi, Saeedeh Zenoozian, M. Lashkari, Pandora Patterson
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摘要

背景癌症进展恐惧(FOP)是癌症患者普遍存在的一个重要问题,包括在积极治疗期间对癌症进展的担忧。FOP 水平升高会导致功能障碍。本研究旨在评估以接纳与承诺疗法(ACT)为基础的干预措施对乳腺癌患者的恐惧进展、焦虑敏感性(AS)和生活质量(QOL)的疗效。方法本研究进行了一项临床试验,涉及 80 名正在接受治疗的 I-III 期乳腺癌患者,这些患者的恐惧进展问卷短表得分大于 34 分。这些患者按 1:1 的比例被随机分配到干预组(每周接受 70 分钟的 5-ACT-bsed 团体治疗)或对照组(接受常规治疗)。在基线、干预后和 3 个月随访三个时间点,使用 ASQ、QLQ-C30、认知融合问卷和接受与行动问卷-II 对包括 FOP、AS、QOL 和 ACT 相关因素在内的变量进行评估。结果采用显著方法证实了基于 ACT 手册的忠实性和可接受性。干预后,仅在 ACT 组观察到 FOP 明显减少(P 值ACT < 0.001;Cohen dACT = 1.099)。此外,在随访中,ACT 组的 FOP 下降幅度更大。此外,与对照组相比,ACT 组除躯体症状分量表外,所有次要变量和 ACT 相关变量均有显著改善。
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A randomized clinical trial: Efficacy of group-based acceptance and commitment therapy program for breast cancer patients with high fear of progression.
BACKGROUND Fear of progression (FOP) is a common and significant concern among cancer patients, encompassing worries about cancer progression during active treatment. Elevated levels of FOP can be dysfunctional. This study aims to assess the efficacy of an Acceptance and Commitment Therapy (ACT)-based intervention on FOP, anxiety sensitivity (AS), and quality of life (QOL) in breast cancer patients. METHODS A clinical trial was conducted involving 80 stage I-III active-treatment breast cancer patients with a score greater than 34 on the Fear of Progression Questionnaire-Short Form scale. These patients were randomly assigned in a 1:1 ratio to either an intervention group, which received weekly 70-min sessions of 5-ACT-bsed group-therapy, or a control group that received usual treatment. Variables including FOP, AS, QOL, and ACT-related factors were assessed using ASQ, QLQ-C30, Cognitive Fusion Questionnaire, and Acceptance and Action Questionnaire-II at three time points: baseline, post-intervention, and 3-month follow-up. The efficacy of the intervention was evaluated using mixed model analysis across all time-points. RESULTS The fidelity and acceptability of the ACT-based manual were confirmed using significant methods. A significant reduction in FOP was observed only in the ACT group at post-intervention (P-valueACT < 0.001; Cohen dACT = 1.099). Furthermore, the ACT group demonstrated a more significant reduction in FOP at follow-up. Furthermore, all secondary and ACT-related variables, except for the physical symptoms subscale, showed significant improvement in the ACT group compared to the control group. CONCLUSIONS Our ACT-based manual showed promise for reducing FOP, AS, and improving QOL, and ACT-related variables in breast cancer patients 3 months following the intervention.
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