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通过电子邮件对少数族裔乳腺癌幸存者进行生活方式干预:随机平行组可行性研究。

A Lifestyle Intervention via Email in Minority Breast Cancer Survivors: Randomized Parallel-Group Feasibility Study.

作者信息

Paxton Raheem J, Hajek Richard, Newcomb Patricia, Dobhal Megha, Borra Sujana, Taylor Wendell C, Parra-Medina Deborah, Chang Shine, Courneya Kerry S, Block Gladys, Block Torin, Jones Lovell A

机构信息

Department of Community Medicine and Population Health, The University of Alabama, Tuscaloosa, AL, United States.

Center for Health Equity and Evaluation Research, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

出版信息

JMIR Cancer. 2017 Sep 21;3(2):e13. doi: 10.2196/cancer.7495.

Abstract

BACKGROUND

Our data have indicated that minority breast cancer survivors are receptive to participating in lifestyle interventions delivered via email or the Web, yet few Web-based studies exist in this population.

OBJECTIVE

The aim of this study was to examine the feasibility and preliminary results of an email-delivered diet and activity intervention program, "A Lifestyle Intervention Via Email (ALIVE)," delivered to a sample of racial and ethnic minority breast cancer survivors.

METHODS

Survivors (mean age: 52 years, 83% [59/71] African American) were recruited and randomized to receive either the ALIVE program's 3-month physical activity track or its 3-month dietary track. The fully automated system provided tools for self-monitoring and goal setting, tailored content, and automated phone calls. Descriptive statistics and mixed-effects models were computed to examine the outcomes of the study.

RESULTS

Upon completion, 44 of 71 survivors completed the study. Our "intention-to-treat" analysis revealed that participants in the physical activity track made greater improvements in moderate to vigorous activity than those in the dietary track (+97 vs. +49 min/week, P<.001). Similarly, reductions in total sedentary time among those in the physical activity track (-304 vs. -59 min/week, P<.001) was nearly 5 times greater than that for participants in the dietary track. Our completers case analysis indicated that participants in the dietary track made improvements in the intake of fiber (+4.4 g/day), fruits and vegetables (+1.0 cup equivalents/day), and reductions in saturated fat (-2.3 g/day) and trans fat (-0.3 g/day) (all P<.05). However, these improvements in dietary intake were not significantly different from the changes observed by participants in the physical activity track (all P>.05). Process evaluation data indicated that most survivors would recommend ALIVE to other cancer survivors (97%), were satisfied with ALIVE (82%), and felt that ALIVE was effective (73%). However, survivors expressed concerns about the functionality of the interactive emails.

CONCLUSIONS

ALIVE appears to be feasible for racial and ethnic minority cancer survivors and showed promising results for larger implementation. Although survivors favored the educational content, a mobile phone app and interactive emails that work on multiple email domains may help to boost adherence rates and to improve satisfaction with the Web-based platform.

TRIAL REGISTRATION

ClinicalTrials.gov NCT02722850; https://clinicaltrials.gov/ct2/show/NCT02722850 (Archived by WebCite at http://www.webcitation.org/6tHN9VsPh).

摘要

背景

我们的数据表明,少数族裔乳腺癌幸存者愿意参与通过电子邮件或网络提供的生活方式干预措施,但针对这一人群的基于网络的研究却很少。

目的

本研究旨在检验一项通过电子邮件提供的饮食与活动干预项目“通过电子邮件进行生活方式干预(ALIVE)”对种族和族裔少数乳腺癌幸存者样本的可行性及初步结果。

方法

招募幸存者(平均年龄:52岁,83%[59/71]为非裔美国人)并随机分组,使其接受ALIVE项目为期3个月的身体活动干预或为期3个月的饮食干预。全自动系统提供自我监测和目标设定工具、个性化内容以及自动电话提醒。计算描述性统计数据和混合效应模型以检验研究结果。

结果

71名幸存者中有44名完成了研究。我们的“意向性分析”显示,身体活动干预组的参与者在中度至剧烈活动方面的改善幅度大于饮食干预组(每周增加97分钟对增加49分钟,P<0.001)。同样,身体活动干预组参与者的久坐总时长减少量(每周减少304分钟对减少59分钟,P<0.001)几乎是饮食干预组参与者的5倍。我们的完成者病例分析表明,饮食干预组参与者在纤维摄入量(每天增加4.4克)、水果和蔬菜摄入量(每天增加1.0杯当量)方面有所改善,饱和脂肪(每天减少2.3克)和反式脂肪(每天减少0.3克)摄入量减少(均P<0.05)。然而,这些饮食摄入量的改善与身体活动干预组参与者的变化并无显著差异(均P>0.05)。过程评估数据表明,大多数幸存者会向其他癌症幸存者推荐ALIVE(97%),对ALIVE感到满意(82%),并认为ALIVE有效(73%)。然而,幸存者对交互式电子邮件的功能表示担忧。

结论

ALIVE对种族和族裔少数癌症幸存者似乎是可行的,并显示出有望进行更大规模实施的结果。尽管幸存者青睐教育内容,但一款适用于多个电子邮件域名的手机应用程序和交互式电子邮件可能有助于提高依从率并提升对基于网络平台的满意度。

试验注册

ClinicalTrials.gov NCT02722850;https://clinicaltrials.gov/ct2/show/NCT02722850(由WebCite存档于http://www.webcitation.org/6tHN9VsPh)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddab/5629346/7e7a63822542/cancer_v3i2e13_fig1.jpg

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