Baik Sharon H, Oswald Laura B, Buscemi Joanna, Buitrago Diana, Iacobelli Francisco, Perez-Tamayo Alejandra, Guitelman Judith, Penedo Frank J, Yanez Betina
Department of Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, United States.
Department of Supportive Care Medicine, City of Hope, Duarte, CA, United States.
JMIR Cancer. 2020 Dec 8;6(2):e17538. doi: 10.2196/17538.
Latina breast cancer survivors experience poorer health-related quality of life (HRQoL), greater symptom burden, and more psychosocial needs compared to non-Latina breast cancer survivors. eHealth platforms such as smartphone apps are increasingly being used to deliver psychosocial interventions to cancer survivors. However, few psychosocial eHealth interventions have been developed specifically for Latina breast cancer survivors. Further, little is known about how Latinas, in general, engage with eHealth interventions and whether specific participant characteristics are associated with app use in this population. We evaluated the use of 2 culturally informed, evidence-based smartphone apps for Latina breast cancer survivors-one that was designed to improve HRQoL and reduce symptom burden (My Guide) and the other to promote healthy lifestyle behaviors (My Health).
The objectives of our study were to explore the patterns of use of the My Guide intervention app and My Health attention-control app among Latina breast cancer survivors.
Eighty Latina breast cancer survivors were randomized to use the My Guide or My Health app for 6 weeks. Assessments were collected at baseline (T1), immediately after the 6-week intervention (T2), and 2 weeks after T2 (T3). Specific study outcomes included subdomains of HRQoL, symptom burden, cancer-specific distress, cancer-relevant self-efficacy, and breast cancer knowledge.
On average, participants used their assigned app for more than 1 hour per week. Sociodemographic or psychological characteristics were not significantly associated with app use, except for employment status in the My Health group. Content related to common physical and emotional symptoms of breast cancer survivors as well as recommendations for nutrition and physical activity were most frequently accessed by My Guide and My Health participants, respectively. Lastly, clinically meaningful improvements were demonstrated in breast cancer well-being among low app users (ie, <60 minutes of use/week) of My Guide and social well-being among high app users (ie, ≥60 minutes of use/week) of My Health.
The favorable rates of participant use across both apps suggest that Latina breast cancer survivors are interested in the content delivered across both My Guide and My Health. Furthermore, since sociodemographic variables, excluding employment status, and baseline HRQoL (psychological variable) were not related to app use, My Guide and My Health may be accessible to diverse Latina breast cancer survivors.
ClinicalTrials.gov NCT03645005; https://clinicaltrials.gov/ct2/show/NCT03645005.
与非拉丁裔乳腺癌幸存者相比,拉丁裔乳腺癌幸存者的健康相关生活质量(HRQoL)较差,症状负担更大,心理社会需求更多。智能手机应用程序等电子健康平台越来越多地被用于为癌症幸存者提供心理社会干预。然而,专门为拉丁裔乳腺癌幸存者开发的心理社会电子健康干预措施很少。此外,对于拉丁裔总体上如何参与电子健康干预以及特定参与者特征是否与该人群的应用程序使用相关,人们了解甚少。我们评估了两款针对拉丁裔乳腺癌幸存者的具有文化针对性、基于证据的智能手机应用程序的使用情况——一款旨在改善HRQoL并减轻症状负担(我的指南),另一款旨在促进健康生活方式行为(我的健康)。
我们研究的目的是探索拉丁裔乳腺癌幸存者中“我的指南”干预应用程序和“我的健康”对照应用程序的使用模式。
80名拉丁裔乳腺癌幸存者被随机分配使用“我的指南”或“我的健康”应用程序6周。在基线(T1)、6周干预结束后立即(T2)以及T2后2周(T3)进行评估。具体研究结果包括HRQoL的子领域、症状负担、癌症特异性困扰、癌症相关自我效能感和乳腺癌知识。
参与者平均每周使用指定应用程序超过1小时。社会人口统计学或心理特征与应用程序使用无显著关联,但“我的健康”组中的就业状况除外。“我的指南”和“我的健康”参与者分别最常访问与乳腺癌幸存者常见身体和情绪症状相关的内容以及营养和体育活动建议。最后,在“我的指南”的低应用程序用户(即每周使用<60分钟)的乳腺癌幸福感和“我的健康”的高应用程序用户(即每周使用≥60分钟)的社交幸福感方面显示出具有临床意义的改善。
两款应用程序的参与者使用率都很高,这表明拉丁裔乳腺癌幸存者对“我的指南”和“我的健康”所提供的内容感兴趣。此外,由于除就业状况外的社会人口统计学变量和基线HRQoL(心理变量)与应用程序使用无关,“我的指南”和“我的健康”可能适用于不同的拉丁裔乳腺癌幸存者。
ClinicalTrials.gov NCT03645005;https://clinicaltrials.gov/ct2/show/NCT03645005 。