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A Web-Based Lifestyle Intervention Aimed at Improving Cognition in Patients With Cancer Returning to Work in an Outpatient Setting: Protocol for a Randomized Controlled Trial

机译:基于网络的生活方式干预旨在改善癌症患者的认知,以便在门诊环境中工作:随机对照试验的协议

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摘要

BackgroundA high percentage of patients with cancer experience cognitive impairment after cancer treatment, resulting in a decreased health-related quality of life and difficulty returning to work. Consequently, there is a need for effective treatment options to improve cognitive functioning in these patients. In a healthy aging population, multidomain web-based lifestyle interventions have been found to be effective in preventing cognitive decline and improving cognitive functioning. ObjectiveThis study aims to investigate the feasibility and effectiveness of the web-based lifestyle intervention Mijn Fitte Brein (My Fit Brain [MFB]) on cognitive functioning in patients with cancer returning to work. MethodsThe study consists of a feasibility study (N=10), followed by a randomized controlled trial (RCT; N=220). Patients will be recruited by their occupational physicians after their return to work following cancer treatment. Mijn Fitte Brein is organized into 4-week cycles in which patients set a lifestyle goal using the Goal Attainment Scale, receive weekly tips and support, and finally evaluate whether they succeeded in achieving this goal. Lifestyle goals are based on 6 domains: physical exercise, diet, sleep, stress, alcohol use, and smoking. In the feasibility study, data on user experience (structured interview) and usability, assessed with the Post-Study System Usability Scale, will be collected and used to optimize Mijn Fitte Brein. In the RCT, patients will be randomized 1:1 between an intervention group and a control group. Patients will be assessed at baseline, 3 months, and 6 months. The primary outcome measure is subjective cognitive functioning, assessed with the Functional Assessment of Cancer Therapy–Cognitive Function (FACT-Cog). Secondary outcome measures are lifestyle, objective cognitive functioning, and work and psychosocial factors. ResultsRecruitment for the feasibility study has started in February 2020. As of July 2020, however, no patients have been enrolled (due to COVID-19 restrictions). The findings of the feasibility study will be used to optimize the Mijn Fitte Brein intervention. Enrollment for the RCT will continue when possible. The feasibility study will take 6 months (including making adjustments to the intervention), and the RCT will take 2 years. The final results are expected in 2024. The results of the feasibility study and the RCT will be published in peer-reviewed journals. ConclusionsThis is the first time the feasibility and efficacy of a multidomain web-based lifestyle intervention will be studied in patients with cancer. If Mijn Fitte Brein is found to be effective in decreasing cognitive complaints in these patients returning to work, it will be a promising treatment option because of being both affordable and accessible. Trial RegistrationNetherlands Trial Register NL8407; https://www.trialregister.nl/trial/8407 International Registered Report Identifier (IRRID)DERR1-10.2196/22670
机译:BackgroundA癌症患者的经验认知障碍的癌症治疗后,导致高比例的生活和困难,恢复工作与健康相关的质量下降。因此,有必要进行有效的治疗方案,以改善认知功能在这些患者。在一个健康的人口老龄化,多领域的基于Web的生活方式干预被认为是有效预防认知功能减退和改善认知功能。 ObjectiveThis研究旨在探讨基于Web的生活方式干预Mijn Fitte BREIN(我最Fit脑[MFB])对认知功能的癌症患者恢复工作的可行性和有效性。 MethodsThe研究包括的可行性研究(N = 10),接着是随机对照试验(RCT; N = 220)的。患者将自己的职业医师的复工以下癌症治疗后,被招募。 Mijn Fitte BREIN分为4周为一个周期中,患者使用设定的目标达成比例生活方式的目标,收到每周提示和支持,最后评估他们是否成功地实现了这一目标。生活目标是根据6个域:体育锻炼,饮食,睡眠,精神紧张,饮酒和吸烟。在可行性研究,用户体验(结构化面试)和可用性数据,评估与后研究系统的可用性比例,将被收集并用于优化Mijn Fitte BREIN。干预组和对照组之间1:在RCT中,患者被随机分配1。患者将在基线,3个月和6个月进行评估。主要结果测量是主观的认知功能,与癌症治疗,认知功能(FACT-COG)的功能评估评估。二次结果的措施是生活方式,客观的认知功能,以及工作和社会心理因素。 ResultsRecruitment的可行性研究在2020年二月开始截至7月到2020年,但是,没有病人已报名(由于COVID-19的限制)。可行性研究的结果将用于优化Mijn Fitte BREIN干预。招生的RCT将尽可能继续。可行性研究报告将于6个月(包括作出调整,干预),以及RCT将需要2年。最终结果预计将在2024年的可行性研究的结果和RCT将在同行评审期刊上发表。 ConclusionsThis是第一次多域的基于Web的生活方式干预的可行性和有效性将癌症患者进行研究。如果发现Mijn Fitte BREIN可有效地减少在这些患者恢复工作的认知投诉,这将是因为是既实惠又访问的有前途的治疗选择。试用RegistrationNetherlands试验注册NL8407; https://www.trialregister.nl/trial/8407国际注册报告标识符(IRRID)DERR1-10.2196 / 22670

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