The Preferences of Patients With Cancer Regarding Apps to Help Meet Their Illness-Related Information Needs: Qualitative Interview Study

被引:11
|
作者
Richards, Rebecca [1 ]
Kinnersley, Paul [2 ]
Brain, Kate [3 ]
Staffurth, John [4 ]
Wood, Fiona [3 ]
机构
[1] Univ Westminster, London, England
[2] Cardiff Univ, Ctr Med Educ, Cardiff, S Glam, Wales
[3] Cardiff Univ, Div Populat Med, Cardiff, S Glam, Wales
[4] Sect Oncol, Palliat Care Med, Cardiff, S Glam, Wales
来源
JMIR MHEALTH AND UHEALTH | 2019年 / 7卷 / 07期
关键词
education; medical; medical information exchange; smartphone; mobile apps; HEALTH; SUPPORT; SATISFACTION; ACTIVATION; IMPACT;
D O I
10.2196/14187
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: The shift from inpatient to outpatient and community cancer care means that more patients with cancer need to manage their condition at home, without the direct supervision of their clinician. Subsequently, research has reported that many patients with cancer have unmet information needs during their illness. Mobile devices, such as mobile phones and tablet computers, provide an opportunity to deliver information to patients remotely. Before designing an app intervention to help patients with cancer to meet their information needs, in-depth qualitative research is required to gain an understanding of the views of the target users. Objective: We aimed to develop an app intervention to help patients meet their illness-related information needs in noninpatient settings. This study explored the information needs of patients with cancer and their preferences for an app and desired app features. Specifically, the perceived acceptability of an app, desired app features, and the potential benefits and disadvantages of, and barriers to, an app were explored. Methods: Qualitative, one-on-one semistructured interviews were conducted with patients with urological, colorectal, breast, or gynecological cancers (N=23) across 2 hospitals in South Wales. Interviews were audio-taped, transcribed, and analyzed using a thematic analysis. Results: Findings indicated that barriers to information exchange and understanding in consultations, and identification of reliable information sources between consultations, appeared to contribute to patients' unmet information needs. Consequently, app feature suggestions included a question prompt list, a glossary of cancer terms, a resources feature, and a contacts feature. Anticipated benefits of this type of app included a more informed patient, improved quality of life, decreased anxiety, and increased confidence to participate in their care. The anticipated barriers to app use are likely to be temporary or can be minimized with regard to these findings during app development and implementation. Conclusions: This study highlights the desire of patients with cancer for an app intervention to help them meet their information needs during and between consultations with their clinicians. This study also highlights the anticipated acceptability and benefits of this type of intervention; however, further research is warranted.
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页数:11
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