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SafeFit 试验:虚拟诊所提供多模式干预措施,以改善癌症患者的心理和身体健康。一项针对 COVID-19 的非随机 III 期试验方案。

SafeFit Trial: virtual clinics to deliver a multimodal intervention to improve psychological and physical well-being in people with cancer. Protocol of a COVID-19 targeted non-randomised phase III trial.

机构信息

School of Health Sciences, University of Southampton, Southampton, UK

NIHR Southampton Biomedical Research Centre, University Hospital Southampton NHS Foundation Trust, Southampton, UK.

出版信息

BMJ Open. 2021 Aug 26;11(8):e048175. doi: 10.1136/bmjopen-2020-048175.

Abstract

INTRODUCTION

The impact of the COVID-19 pandemic (caused by the SARS-CoV-2 virus) on individuals with cancer has been profound. It has led to increased anxiety, distress and deconditioning due to reduced physical activity. We aim to investigate whether SafeFit, a multimodal intervention of physical activity, nutrition and psychological support delivered virtually by cancer exercise specialists (CES), can improve physical and emotional functionings during the COVID-19 pandemic.

METHODS AND ANALYSIS

A phase III non-randomised intervention trial, target recruitment of 1050 adults with suspected or confirmed diagnosis of cancer. All recruited participants will receive the multimodal intervention delivered by CES for 6 months. Sessions will be delivered 1-to-1 using telephone/video conferencing consultations. CES will work with each participant to devise a personalised programme of (1) physical activity, (2) basic dietary advice and (3) psychological support, all underpinned by behaviour change support.

PRIMARY OUTCOME

Physical and emotional functioning as measured by the European Organisation for Research and Treatment of Cancer-Quality of Life Questionnaire (EORTC-QLQ-C30).

SECONDARY OUTCOMES

overall quality of life measured by EORTC-QLQ-C30 and EQ-5D-5L, health economics, patient activation, self-efficacy to self-manage chronic disease, distress, impact of COVID-19 on emotional functioning, self-reported physical activity, functional capacity and nutrition. Adherence to the intervention will also be measured and a process evaluation conducted.

ETHICS AND DISSEMINATION

Ethical approval was obtained from the Health Research Authority (reference number 20/NW/0254). Results of this trial will be disseminated through publication of peer-reviewed articles, presentations at scientific conferences, and to the public and people with cancer in collaboration with our patient and public involvement representatives and partners.

TRIAL REGISTRATION NUMBER

NCT04425616.

摘要

简介

由 SARS-CoV-2 病毒引起的 COVID-19 大流行对癌症患者产生了深远影响。由于身体活动减少,导致焦虑、痛苦和身体机能下降。我们旨在研究由癌症运动专家(CES)通过虚拟方式提供的多模式干预措施(包括身体活动、营养和心理支持)是否可以改善 COVID-19 大流行期间的身体和情绪功能。

方法和分析

这是一项 III 期非随机干预试验,目标招募 1050 名疑似或确诊癌症的成年人。所有入组的参与者将接受 CES 提供的为期 6 个月的多模式干预。将通过电话/视频会议咨询进行 1 对 1 的会议。CES 将与每位参与者合作制定个性化的计划,包括(1)身体活动、(2)基本饮食建议和(3)心理支持,所有计划都以行为改变支持为基础。

主要结局

采用欧洲癌症研究与治疗组织生活质量问卷(EORTC-QLQ-C30)评估身体和情绪功能。

次要结局

EORTC-QLQ-C30 和 EQ-5D-5L 评估整体生活质量,健康经济学,患者激活,自我管理慢性病的自我效能,痛苦,COVID-19 对情绪功能的影响,自我报告的身体活动,功能能力和营养。还将测量干预措施的依从性,并进行过程评估。

伦理和传播

该试验已获得英国健康研究机构(编号 20/NW/0254)的伦理批准。将通过同行评议文章的发表、科学会议的演讲,以及与我们的患者和公众参与代表和合作伙伴合作,向公众和癌症患者传播试验结果。

试验注册号

NCT04425616。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f8/8392740/53480e4a3dab/bmjopen-2020-048175f01.jpg

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