提高生活质量和支持预先护理计划的正念:针对晚期癌症患者及其家庭护理者的试点随机对照试验。

IF 2.5 2区 医学 Q2 HEALTH CARE SCIENCES & SERVICES BMC Palliative Care Pub Date : 2024-09-28 DOI:10.1186/s12904-024-01564-7
Catherine E Mosher, Kathleen A Beck-Coon, Wei Wu, Ashley B Lewson, Patrick V Stutz, Linda F Brown, Qing Tang, Paul R Helft, Kristin Levoy, Susan E Hickman, Shelley A Johns
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引用次数: 0

摘要

背景:晚期癌症患者和家庭照顾者经常采用回避的应对策略,例如推迟预先护理计划的讨论,这导致了他们生活质量的下降。以正念为基础的干预措施在改善这类人群的生活质量方面已初见成效,但却很少应用于预先护理计划。这项试点试验考察了以小组为基础的正念提高生活质量和支持晚期护理规划(MEANING)干预对晚期癌症患者和护理者二人组的初步疗效。主要结果是患者和护理者的生活质量或幸福感,次要结果包括患者参与晚期护理规划(自我效能和准备程度)以及其他心理和症状结果:在这项试点试验中,从美国中西部地区的五家肿瘤诊所招募了晚期癌症患者,并将他们随机分配到每周六节的正念干预小组课程(33 人)或常规护理(22 人)中。结果通过基线、干预后和干预后 1 个月的调查进行评估。所有可用数据均纳入评估干预效果的多层次模型中:结果:在 "有意义 "条件下,患者的存在感和预先护理规划自我效能感在随访期间均有显著提高,而常规护理患者则没有。其他结果的组间差异无统计学意义。这些结果包括患者幸福感的其他方面、护理者的生活质量、患者对预先护理计划的准备程度、护理者的负担、患者和护理者的抑郁症状、焦虑、睡眠障碍、认知回避以及对癌症的平静接受。然而,只有 MEANING 患者的心理健康水平在各次随访中均有适度提高,而 MEANING 护理人员的生活质量在 1 个月的随访中也有适度提高。某些心理结果,如随访 1 个月时护理人员的负担,在 "有意义 "条件下也有适度改善。两种情况下的患者都报告说,他们参与预先护理计划的准备程度都有小到中等程度的提高:基于正念的干预有望改善晚期癌症患者和照护者的生活质量和预先护理规划结果,值得进一步试验:试验注册:ClinicalTrials.gov NCT03257007。注册时间:2017 年 8 月 22 日,https://clinicaltrials.gov/ct2/show/NCT03257007 。
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Mindfulness to enhance quality of life and support advance care planning: a pilot randomized controlled trial for adults with advanced cancer and their family caregivers.

Background: Patients with advanced cancer and family caregivers often use avoidant coping strategies, such as delaying advance care planning discussions, which contribute to deterioration in their quality of life. Mindfulness-based interventions have shown promise in improving quality of life in this population but have rarely been applied to advance care planning. This pilot trial examined the preliminary efficacy of a group-based Mindfulness to Enhance Quality of Life and Support Advance Care Planning (MEANING) intervention for patient-caregiver dyads coping with advanced cancer. Primary outcomes were patient and caregiver quality of life or well-being, and secondary outcomes included patient advanced care planning engagement (self-efficacy and readiness) and other psychological and symptom outcomes.

Methods: In this pilot trial, dyads coping with advanced cancer were recruited from five oncology clinics in the midwestern U.S. and randomized to six weekly group sessions of a mindfulness intervention (n = 33 dyads) or usual care (n = 22 dyads). Outcomes were assessed via surveys at baseline, post-intervention, and 1 month post-intervention. All available data were included in the multilevel models assessing intervention efficacy.

Results: Patients in the MEANING condition experienced significant increases in existential well-being and self-efficacy for advance care planning across follow-ups, whereas usual care patients did not. Other group differences in outcomes were not statistically significant. These outcomes included other facets of patient well-being, caregiver quality of life, patient readiness for advance care planning, caregiver burden, and patient and caregiver depressive symptoms, anxiety, sleep disturbance, cognitive avoidance, and peaceful acceptance of cancer. However, only MEANING patients showed moderate increases in psychological well-being across follow-ups, and MEANING caregivers showed moderate increases in quality of life at 1-month follow-up. Certain psychological outcomes, such as caregiver burden at 1-month follow-up, also showed moderate improvement in the MEANING condition. Patients in both conditions reported small to moderate increases in readiness to engage in advance care planning.

Conclusions: A mindfulness-based intervention showed promise in improving quality-of-life and advance care planning outcomes in patients and caregivers coping with advanced cancer and warrants further testing.

Trial registration: ClinicalTrials.gov NCT03257007. Registered 22 August 2017, https://clinicaltrials.gov/ct2/show/NCT03257007 .

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来源期刊
BMC Palliative Care
BMC Palliative Care HEALTH CARE SCIENCES & SERVICES-
CiteScore
4.60
自引率
9.70%
发文量
201
审稿时长
21 weeks
期刊介绍: BMC Palliative Care is an open access journal publishing original peer-reviewed research articles in the clinical, scientific, ethical and policy issues, local and international, regarding all aspects of hospice and palliative care for the dying and for those with profound suffering related to chronic illness.
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