Klafke Nadja, Mahler Cornelia, von Hagens Cornelia, Rochon Justine, Schneeweiss Andreas, Müller Andreas, Salize Hans-Joachim, Joos Stefanie
Department of General Practice and Health Services Research, University Hospital Heidelberg, Voßstr. 2, D-69115, Heidelberg, Germany.
Department of Gynaecological Endocrinology and Reproductive Medicine, University Women's Hospital Heidelberg, Im Neuenheimer Feld 440, D-69120, Heidelberg, Germany.
Trials. 2015 Feb 15;16:51. doi: 10.1186/s13063-014-0538-4.
Health-related quality of life (HRQoL) is most adversely affected in cancer patients between diagnosis and the end of chemotherapy. The aim of the Complementary Nursing in Gynecologic Oncology (CONGO) study is to assess the effectiveness of a complex nursing care intervention of CAM to increase HRQoL in cancer patients undergoing chemotherapy.
METHODS/DESIGN: CONGO is a prospective partially randomized patient preference (PRPP) trial including adult women diagnosed with breast and gynecologic cancer starting a new chemotherapy regimen. Patients without strong preferences for CAM will be randomized to usual nursing care or complex nursing care; those patients with strong preferences will be allowed their choice. The intervention consists of three interacting and intertwined elements: CAM nursing intervention packet, counseling on CAM using a resource-oriented approach and evidence-based informational material on CAM. Primary outcome data on participants' HRQoL will be collected from baseline until the end of treatment and long-term follow-up using the EORTC-QLQ-C30. Secondary outcomes include nausea, fatigue, pain, anxiety/depression, social support, self-efficacy, patient competence, spiritual wellbeing, and satisfaction with care. Accompanying research on economic outcomes as well as a mixed-methods process evaluation will be conducted. A total of 590 patients (236 patients in the randomized part of the study and 354 patients in the observational part of the study) will be recruited in the two outpatient clinics. The first analysis step will be the intention-to-treat (ITT) analysis of the randomized part of the trial. A linear mixed model will be used to compare the continuous primary endpoint between the intervention and control arm of the randomized group. The observational part of the trial will be analyzed descriptively. External validity will be assessed by comparing randomized with nonrandomized patients.
Cancer patients are increasingly using CAM as supportive cancer care, however, a patient-centered model of care that includes CAM for the patient during chemotherapy still needs to be evaluated. This protocol has been designed to test if the effects of the intervention go beyond potential benefits in quality-of-life outcomes.
German Clinical Trials Register (DRKS), DRKS00006056 (15 April 2014).
在癌症患者从确诊到化疗结束期间,与健康相关的生活质量(HRQoL)受到的负面影响最为严重。妇科肿瘤辅助护理(CONGO)研究的目的是评估一种综合的补充替代医学(CAM)护理干预措施对提高接受化疗的癌症患者HRQoL的有效性。
方法/设计:CONGO是一项前瞻性部分随机患者偏好(PRPP)试验,纳入开始新化疗方案的成年女性乳腺癌和妇科癌症患者。对CAM没有强烈偏好的患者将被随机分配到常规护理或综合护理;有强烈偏好的患者将允许其自行选择。干预措施包括三个相互作用和交织的要素:CAM护理干预包、采用资源导向方法的CAM咨询以及基于证据的CAM信息材料。将使用欧洲癌症研究与治疗组织生活质量问卷核心30项(EORTC-QLQ-C30)从基线到治疗结束及长期随访收集参与者HRQoL的主要结局数据。次要结局包括恶心、疲劳、疼痛、焦虑/抑郁、社会支持、自我效能感、患者能力、精神健康以及对护理的满意度。将进行伴随的经济结局研究以及混合方法过程评估。将在两家门诊诊所招募总共590名患者(研究随机部分236名患者,研究观察部分354名患者)。第一个分析步骤将是对试验随机部分的意向性分析(ITT)。将使用线性混合模型比较随机组干预组和对照组之间的连续主要终点。试验的观察部分将进行描述性分析。将通过比较随机患者和非随机患者来评估外部效度。
癌症患者越来越多地将CAM用作癌症支持性护理,然而,一种以患者为中心的护理模式,即在化疗期间为患者纳入CAM,仍有待评估。本方案旨在测试干预措施的效果是否超出生活质量结局方面的潜在益处。
德国临床试验注册中心(DRKS),DRKS00006056(2014年4月15日)。