首页> 外文期刊>BMJ Open >A pilot randomised controlled trial of personalised care after treatment for prostate cancer (TOPCAT-P): nurse-led holistic-needs assessment and individualised psychoeducational intervention: study protocol
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A pilot randomised controlled trial of personalised care after treatment for prostate cancer (TOPCAT-P): nurse-led holistic-needs assessment and individualised psychoeducational intervention: study protocol

机译:前列腺癌治疗后个性化护理的先导性随机对照试验(TOPCAT-P):护士指导的整体需求评估和个性化的心理教育干预:研究方案

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Introduction Prostate cancer is common and the incidence is increasing, but more men are living longer after diagnosis, and die with their disease rather than of it. Nonetheless, specific and substantial physical, sexual, emotional and mental health problems often lead to a poor quality of life. Urology services increasingly struggle to cope with the demands of follow-up care, and primary care is likely to play the central role in long-term follow-up. The present phase II trial will evaluate the feasibility and acceptability of a nurse-led, person-centred psychoeducational intervention, delivered in community or primary care settings. Methods and analysis Prostate cancer survivors diagnosed in the past 9–48?months and currently biochemically stable will be identified from hospital records by their treating clinician. Eligible men would have either completed radical treatment, or would be followed up with prostate specific antigen monitoring and symptom reporting. We will recruit 120 patients who will be randomised to receive either an augmented form of usual care, or an additional nurse-led intervention for a period of 36?weeks. Following the health policy in Wales, the intervention is offered by a key worker, is promoting prudent healthcare and is using a holistic needs assessment. Outcome measures will assess physical symptoms, psychological well-being, confidence in managing own health and quality of life. Healthcare service use will be measured over 36?weeks. Feedback interviews with patients and clinicians will further inform the acceptability of the intervention. Recruitment, attrition, questionnaire completion rates and outcome measures variability will be assessed, and results will inform the design of a future phase III trial and accompanying economic evaluation. Ethics and dissemination Ethics approval was granted by Bangor University and North Wales REC (13/WA/0291). Results will be reported in peer-reviewed publications, at scientific conferences, and directly through national cancer and primary care networks. Trial registration number ISRCTN 34516019.
机译:引言前列腺癌很常见,并且发病率正在增加,但是更多的男性在被诊断后寿命更长,并且死于疾病而不是死于疾病。但是,具体的和实质性的身体,性,情感和精神健康问题常常导致生活质量低下。泌尿科服务越来越难以满足后续护理的需求,而初级保健很可能在长期随访中发挥核心作用。目前的第二阶段试验将评估在社区或初级保健环境中实施的以护士为中心的以人为本的心理教育干预措施的可行性和可接受性。方法和分析在过去9-48个月内被诊断出并目前生化稳定的前列腺癌幸存者将由其治疗医生从医院记录中识别出来。符合条件的男性将完成根治性治疗,或者接受前列腺特异性抗原监测和症状报告的随访。我们将招募120名患者,这些患者将随机接受增强形式的常规护理,或​​在36周内接受额外的护士主导干预。根据威尔士的卫生政策,干预由一名主要工人提供,正在促进谨慎的医疗保健,并使用整体需求评估。结果措施将评估身体症状,心理健康,对管理自己的健康和生活质量的信心。医疗保健服务的使用将超过36周。对患者和临床医生的反馈访谈将进一步告知干预措施的可接受性。将评估招聘,损耗,问卷完成率和结果度量的可变性,其结果将为将来的第三阶段试验的设计和相应的经济评估提供依据。道德规范和传播道德规范获得了Bangor大学和北威尔士REC(13 / WA / 0291)的批准。研究结果将在同行评审的出版物,科学会议上直接通过国家癌症和初级保健网络进行报告。试用注册号ISRCTN 34516019。

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