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老年癌症幸存者功能活动能力和力量的远程评估:一项效度和信度研究方案

Remote Assessment of Functional Mobility and Strength in Older Cancer Survivors: Protocol for a Validity and Reliability Study.

作者信息

Blair Cindy K, Harding Elizabeth, Herman Carla, Boyce Tawny, Demark-Wahnefried Wendy, Davis Sally, Kinney Anita Y, Pankratz Vernon S

机构信息

Department of Internal Medicine, University of New Mexico, Albuquerque, NM, United States.

Comprehensive Cancer Center, University of New Mexico, Albuquerque, NM, United States.

出版信息

JMIR Res Protoc. 2020 Sep 1;9(9):e20834. doi: 10.2196/20834.

Abstract

BACKGROUND

Older cancer survivors, faced with both age- and treatment-related morbidity, are at increased and premature risk for physical function limitations. Physical performance is an important predictor of disability, quality of life, and premature mortality, and thus is considered an important target of interventions designed to prevent, delay, or attenuate the physical functional decline. Currently, low-cost, valid, and reliable methods to remotely assess physical performance tests that are self-administered by older adults in the home-setting do not exist, thus limiting the reach, scalability, and dissemination of interventions.

OBJECTIVE

This paper will describe the rationale and design for a study to evaluate the accuracy, reliability, safety, and acceptability of videoconferencing and self-administered tests of functional mobility and strength by older cancer survivors in their own homes.

METHODS

To enable remote assessment, participants receive a toolkit and instructions for setting up their test course and communicating with the investigator. Two standard gerontologic performance tests are being evaluated: the Timed Up and Go test and the 30-second chair stand test. Phase 1 of the study evaluates proof-of-concept that older cancer survivors (age ≥60 years) can follow the testing protocol and use a tablet PC to communicate with the study investigator. Phase 2 evaluates the criterion validity of videoconference compared to direct observation of the two physical performance tests. Phase 3 evaluates reliability by enrolling 5-10 participants who agree to repeat the remote assessment (without direct observation). Phase 4 enrolls 5-10 new study participants to complete the remote assessment test protocol. Feedback from participants in each phase is used to refine the test protocol and instructions.

RESULTS

Enrollment began in December 2019. Ten participants completed the Phase 1 proof-of-concept. The study was paused in mid-March 2020 due to the COVID-19 pandemic. The study is expected to be completed by the end of 2020.

CONCLUSIONS

This validity and reliability study will provide important information on the acceptability and safety of using videoconferencing to remotely assess two tests of functional mobility and strength, self-administered by older adults in their homes. Videoconferencing has the potential to expand the reach, scalability, and dissemination of interventions to older cancer survivors, and potentially other older adults, especially in rural areas.

TRIAL REGISTRATION

ClinicalTrials.gov NCT04339959; https://clinicaltrials.gov/ct2/show/NCT04339959.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/20834.

摘要

背景

老年癌症幸存者面临与年龄和治疗相关的发病率问题,身体功能受限的风险增加且出现过早。身体表现是残疾、生活质量和过早死亡的重要预测指标,因此被视为旨在预防、延缓或减轻身体功能衰退的干预措施的重要目标。目前,不存在低成本、有效且可靠的方法来远程评估老年人在家庭环境中自行进行的身体表现测试,这限制了干预措施的覆盖范围、可扩展性和传播。

目的

本文将描述一项研究的基本原理和设计,以评估视频会议以及老年癌症幸存者在自己家中自行进行的功能移动性和力量测试的准确性、可靠性、安全性和可接受性。

方法

为实现远程评估,参与者会收到一个工具包以及关于设置测试路线和与研究者沟通的说明。正在评估两项标准的老年医学表现测试:定时起立行走测试和30秒坐立测试。研究的第一阶段评估概念验证,即老年癌症幸存者(年龄≥60岁)能否遵循测试方案并使用平板电脑与研究研究者进行沟通。第二阶段评估视频会议与直接观察两项身体表现测试相比的标准效度。第三阶段通过招募5至10名同意重复远程评估(无直接观察)的参与者来评估可靠性。第四阶段招募5至10名新的研究参与者来完成远程评估测试方案。每个阶段参与者的反馈用于完善测试方案和说明。

结果

2019年12月开始招募。10名参与者完成了第一阶段的概念验证。由于2019冠状病毒病大流行,该研究于2020年3月中旬暂停。预计该研究将于2020年底完成。

结论

这项效度和可靠性研究将提供关于使用视频会议远程评估老年人在家庭中自行进行的两项功能移动性和力量测试的可接受性和安全性的重要信息。视频会议有可能扩大对老年癌症幸存者以及潜在的其他老年人,特别是农村地区老年人的干预措施的覆盖范围、可扩展性和传播。

试验注册

ClinicalTrials.gov NCT04339959;https://clinicaltrials.gov/ct2/show/NCT04339959。

国际注册报告标识符(IRRID):DERR1-10.2196/20834。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/061f/7492978/f73c714e6390/resprot_v9i9e20834_fig1.jpg

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