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      Development and Evaluation of a Digital Intervention for Fulfilling the Needs of Older Migrant Patients With Cancer: User-Centered Design Approach

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          Abstract

          Background

          Older migrant patients with cancer face many language- and culture-related barriers to patient participation during medical consultations. To bridge these barriers, an eHealth tool called Health Communicator was developed in the Netherlands. Essentially used as a digital translator that can collect medical history information from patients, the Health Communicator did not include an oncological module so far, despite the fact that the prevalence of Dutch migrant patients with cancer is rising.

          Objective

          This study aims to systematically develop, implement, and conduct a pilot evaluation of an oncological module that can be integrated into the Health Communicator to stimulate patient participation among older Turkish-Dutch and Moroccan-Dutch patients with cancer.

          Methods

          The Spiral Technology Action Research model, which incorporates 5 cycles that engage key stakeholders in intervention development, was used as a framework. The listen phase consisted of a needs assessment. The plan phase consisted of developing the content of the oncological module, namely the question prompt lists (QPLs) and scripts for patient education videos. On the basis of pretests in the do phase, 6 audiovisual QPLs on patient rights, treatment, psychosocial support, lifestyle and access to health care services, patient preferences, and clinical trials were created. Additionally, 5 patient education videos were created about patient rights, psychosocial support, clinical trials, and patient-professional communication. In the study phase, the oncological module was pilot-tested among 27 older Turkish-Dutch and Moroccan-Dutch patients with cancer during their consultations. In the act phase, the oncological model was disseminated to practice.

          Results

          The patient rights QPL was chosen most often during the pilot testing in the study phase. Patients and health care professionals perceived the QPLs as easy to understand and useful. There was a negative correlation between the tool’s ease of use and patient age. Patients reported that using the module impacted the consultations positively and thought they were more active compared with previous consultations. Health care professionals also found patients to be more active than usual. Health care professionals asked significantly more questions than patients during consultations. Patients requested to see the patients’ rights video most often. Patients rated the videos as easy to understand, useful, and informative. Most of the patients wanted to use the tool in the future.

          Conclusions

          Older migrant patients with cancer, survivors, and health care professionals found the oncological module to be a useful tool and have shown intentions to incorporate it into future consultation sessions. Both QPLs and videos were evaluated positively, the latter indicating that the use of narratives to inform older, low-literate migrant patients with cancer about health-related topics in their mother tongue is a viable approach to increase the effectiveness of health care communication with this target group.

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          Most cited references48

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          Toward a Theory of Entertainment Persuasion: Explaining the Persuasive Effects of Entertainment-Education Messages

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            Understanding tailoring in communicating about health.

            'Tailoring' refers to any of a number of methods for creating communications individualized for their receivers, with the expectation that this individualization will lead to larger intended effects of these communications. Results so far have been generally positive but not consistently so, and this paper seeks to explicate tailoring to help focus future research. Tailoring involves either or both of two classes of goals (enhancing cognitive preconditions for message processing and enhancing message impact through modifying behavioral determinants of goal outcomes) and employs strategies of personalization, feedback and content matching. These goals and strategies intersect in a 2 x 3 matrix in which some strategies and their component tactics match better to some goals than to others. The paper illustrates how this framework can be systematically applied in generating research questions and identifying appropriate study designs for tailoring research.
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              Patient empowerment, patient participation and patient-centeredness in hospital care: A concept analysis based on a literature review.

              The concepts of patient empowerment, patient participation and patient-centeredness have been introduced as part of the trend towards a more participatory health care and have largely been used interchangeably. Although these concepts have been discussed for a number of years, their exact meaning in hospital care remains somewhat unclear. This absence of theoretical and conceptual clarity has led to (1) poor understanding and communication among researchers, health practitioners and policy makers and (2) problems in measurement and comparison between studies across different hospitals.
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                Author and article information

                Contributors
                Journal
                J Med Internet Res
                J Med Internet Res
                JMIR
                Journal of Medical Internet Research
                JMIR Publications (Toronto, Canada )
                1439-4456
                1438-8871
                October 2020
                26 October 2020
                : 22
                : 10
                : e21238
                Affiliations
                [1 ] Department of Communication Science Amsterdam School of Communication Research/ASCoR University of Amsterdam Amsterdam Netherlands
                [2 ] Department of Public and Occupational Health Amsterdam UMC Vrije Universiteit Amsterdam Amsterdam Netherlands
                [3 ] Department of Primary and Community Care Radboud University Medical Centre Nijmegen Netherlands
                Author notes
                Corresponding Author: Hande Sungur h.sungur@ 123456uva.nl
                Author information
                https://orcid.org/0000-0003-4301-8668
                https://orcid.org/0000-0002-1228-1685
                https://orcid.org/0000-0001-6827-5332
                https://orcid.org/0000-0002-4994-4008
                https://orcid.org/0000-0002-2259-5864
                https://orcid.org/0000-0001-8910-0128
                Article
                v22i10e21238
                10.2196/21238
                7652697
                33104008
                da5aa90e-0cbf-4c58-8923-2290f229fb0d
                ©Hande Sungur, Nida Gizem Yılmaz, Brittany Ming Chu Chan, Maria E T C van den Muijsenbergh, Julia C M van Weert, Barbara C Schouten. Originally published in the Journal of Medical Internet Research (http://www.jmir.org), 26.10.2020.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in the Journal of Medical Internet Research, is properly cited. The complete bibliographic information, a link to the original publication on http://www.jmir.org/, as well as this copyright and license information must be included.

                History
                : 8 June 2020
                : 11 July 2020
                : 5 September 2020
                : 7 September 2020
                Categories
                Original Paper
                Original Paper

                Medicine
                cancer,patient participation,health services needs and demand,ehealth,migrants,physician-patient relations,culture,mobile phone

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