Mayo-Gamble Tilicia L, Quasie-Woode Delores, Cunningham-Erves Jennifer, Rollins Margo, Schlundt David, Bonnet Kemberlee, Murry Velma McBride
Department of Health Policy and Community Health, Jiann-Ping Hsu College of Public Health, Georgia Southern University, Statesboro, GA, United States.
Center for Disease Control and Prevention Foundation, Atlanta, GA, United States.
JMIR Form Res. 2021 Nov 30;5(11):e28678. doi: 10.2196/28678.
Individuals with sickle cell disease (SCD) and their caregivers may benefit from technology-based resources to improve disease self-management.
This study explores the preferences regarding a mobile health (mHealth) app to facilitate self-management in adults with SCD and their caregivers living in urban and rural communities.
Five community listening sessions were conducted in 2 urban and rural communities among adults with SCD and their caregivers (N=43). Each session comprised 4 to 15 participants. Participants were asked questions on methods of finding information about SCD self-care, satisfaction with current methods for finding SCD management information, support for SCD management, important features for development of an mHealth app, and areas of benefit for using an mHealth app for SCD self-management. An inductive-deductive content analysis approach was implemented to identify the critical themes.
Seven critical themes emerged, including the current methods for receiving self-management information, desired information, recommendations for communicating sickle cell self-management information, challenges of disease management, types of support received for disease management, barriers to and facilitators of using an mHealth app, and feature preferences for an mHealth app. In addition, we found that the participants were receptive to using mHealth apps in SCD self-management.
This study expands our knowledge on the use of mHealth technology to reduce information access barriers pertaining to SCD. The findings can be used to develop a patient-centered, user-friendly mHealth app to facilitate disease self-management, thus increasing access to resources for families of patients with SCD residing in rural communities.
镰状细胞病(SCD)患者及其护理人员可能会从基于技术的资源中受益,以改善疾病自我管理。
本研究探讨了关于移动健康(mHealth)应用程序的偏好,以促进居住在城市和农村社区的成年SCD患者及其护理人员的自我管理。
在2个城市和农村社区对成年SCD患者及其护理人员(N = 43)进行了5次社区听证会。每次会议有4至15名参与者。向参与者询问了有关查找SCD自我护理信息的方法、对当前查找SCD管理信息方法的满意度、对SCD管理的支持、mHealth应用程序开发的重要功能以及使用mHealth应用程序进行SCD自我管理的受益领域等问题。采用归纳-演绎内容分析法来确定关键主题。
出现了七个关键主题,包括当前接收自我管理信息的方法、所需信息、传播镰状细胞自我管理信息的建议、疾病管理的挑战、疾病管理获得的支持类型、使用mHealth应用程序的障碍和促进因素以及mHealth应用程序的功能偏好。此外,我们发现参与者愿意在SCD自我管理中使用mHealth应用程序。
本研究扩展了我们对使用mHealth技术减少与SCD相关的信息获取障碍的认识。这些发现可用于开发以患者为中心、用户友好的mHealth应用程序,以促进疾病自我管理,从而增加居住在农村社区的SCD患者家庭获得资源的机会。