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      Improving Electronic Survey Response Rates Among Cancer Center Patients During the COVID-19 Pandemic: Mixed Methods Pilot Study

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          Abstract

          Background

          Surveys play a vital role in cancer research. During the COVID-19 pandemic, the use of electronic surveys is crucial to improve understanding of the patient experience. However, response rates to electronic surveys are often lower compared with those of paper surveys.

          Objective

          The aim of this study was to determine the best approach to improve response rates for an electronic survey administered to patients at a cancer center during the COVID-19 pandemic.

          Methods

          We contacted 2750 patients seen at Moffitt Cancer Center in the prior 5 years via email to complete a survey regarding their experience during the COVID-19 pandemic, with patients randomly assigned to a series of variations of prenotifications (ie, postcard, letter) or incentives (ie, small gift, modest gift card). In total, eight combinations were evaluated. Qualitative interviews were conducted to understand the level of patient understanding and burden with the survey, and quantitative analysis was used to evaluate the response rates between conditions.

          Results

          A total of 262 (9.5%) patients completed the survey and 9 participated in a qualitative interview. Interviews revealed minimal barriers in understanding or burden, which resulted in minor survey design changes. Compared to sending an email only, sending a postcard or letter prior to the email improved response rates from 3.7% to 9.8%. Similarly, inclusion of an incentive significantly increased the response rate from 5.4% to 16.7%, especially among racial (3.0% to 12.2%) and ethnic (6.4% to 21.0%) minorities, as well as among patients with low socioeconomic status (3.1% to 14.9%).

          Conclusions

          Strategies to promote effective response rates include prenotification postcards or letters as well as monetary incentives. This work can inform future survey development to increase response rates for electronic surveys, particularly among hard-to-reach populations.

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          Most cited references48

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          Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.

          Research electronic data capture (REDCap) is a novel workflow methodology and software solution designed for rapid development and deployment of electronic data capture tools to support clinical and translational research. We present: (1) a brief description of the REDCap metadata-driven software toolset; (2) detail concerning the capture and use of study-related metadata from scientific research teams; (3) measures of impact for REDCap; (4) details concerning a consortium network of domestic and international institutions collaborating on the project; and (5) strengths and limitations of the REDCap system. REDCap is currently supporting 286 translational research projects in a growing collaborative network including 27 active partner institutions.
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            The REDCap consortium: Building an international community of software platform partners

            The Research Electronic Data Capture (REDCap) data management platform was developed in 2004 to address an institutional need at Vanderbilt University, then shared with a limited number of adopting sites beginning in 2006. Given bi-directional benefit in early sharing experiments, we created a broader consortium sharing and support model for any academic, non-profit, or government partner wishing to adopt the software. Our sharing framework and consortium-based support model have evolved over time along with the size of the consortium (currently more than 3200 REDCap partners across 128 countries). While the "REDCap Consortium" model represents only one example of how to build and disseminate a software platform, lessons learned from our approach may assist other research institutions seeking to build and disseminate innovative technologies.
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              Health literacy and public health: A systematic review and integration of definitions and models

              Background Health literacy concerns the knowledge and competences of persons to meet the complex demands of health in modern society. Although its importance is increasingly recognised, there is no consensus about the definition of health literacy or about its conceptual dimensions, which limits the possibilities for measurement and comparison. The aim of the study is to review definitions and models on health literacy to develop an integrated definition and conceptual model capturing the most comprehensive evidence-based dimensions of health literacy. Methods A systematic literature review was performed to identify definitions and conceptual frameworks of health literacy. A content analysis of the definitions and conceptual frameworks was carried out to identify the central dimensions of health literacy and develop an integrated model. Results The review resulted in 17 definitions of health literacy and 12 conceptual models. Based on the content analysis, an integrative conceptual model was developed containing 12 dimensions referring to the knowledge, motivation and competencies of accessing, understanding, appraising and applying health-related information within the healthcare, disease prevention and health promotion setting, respectively. Conclusions Based upon this review, a model is proposed integrating medical and public health views of health literacy. The model can serve as a basis for developing health literacy enhancing interventions and provide a conceptual basis for the development and validation of measurement tools, capturing the different dimensions of health literacy within the healthcare, disease prevention and health promotion settings.
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                Author and article information

                Contributors
                Journal
                JMIR Cancer
                JMIR Cancer
                JC
                JMIR Cancer
                JMIR Publications (Toronto, Canada )
                2369-1999
                Jul-Sep 2021
                6 August 2021
                6 August 2021
                : 7
                : 3
                : e30265
                Affiliations
                [1 ] Department of Cancer Epidemiology Moffitt Cancer Center Tampa, FL United States
                [2 ] Participant Research, Interventions, and Measurements Core Moffitt Cancer Center Tampa, FL United States
                [3 ] The AltaMed Institute for Health Equity Los Angeles, CA United States
                [4 ] Department of Health Outcomes and Behavior Moffitt Cancer Center Tampa, FL United States
                [5 ] Huntsman Cancer Institute Salt Lake City, UT United States
                [6 ] Department of Population Health Sciences University of Utah Salt Lake City, UT United States
                [7 ] Departments of Medicine and Psychology University of Miami Coral Gables, FL United States
                [8 ] Department of Epidemiology Harvard T.H. Chan School of Public Health Boston, MA United States
                Author notes
                Corresponding Author: Shelley S Tworoger Shelley.Tworoger@ 123456moffitt.org
                Author information
                https://orcid.org/0000-0002-2919-0499
                https://orcid.org/0000-0002-8707-7072
                https://orcid.org/0000-0003-3978-8379
                https://orcid.org/0000-0003-3569-9344
                https://orcid.org/0000-0002-3171-8045
                https://orcid.org/0000-0003-1779-2510
                https://orcid.org/0000-0003-3645-3960
                https://orcid.org/0000-0002-4502-1695
                https://orcid.org/0000-0002-2780-0417
                https://orcid.org/0000-0002-6986-7046
                https://orcid.org/0000-0001-5108-5735
                Article
                v7i3e30265
                10.2196/30265
                8360334
                34156965
                55be7a38-3562-4726-bba2-772e209d249c
                ©Cassandra A Hathaway, Melody N Chavez, Mika Kadono, Dana Ketcher, Dana E Rollison, Erin M Siegel, Anita R Peoples, Cornelia M Ulrich, Frank J Penedo, Shelley S Tworoger, Brian D Gonzalez. Originally published in JMIR Cancer (https://cancer.jmir.org), 06.08.2021.

                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 JMIR Cancer, is properly cited. The complete bibliographic information, a link to the original publication on https://cancer.jmir.org/, as well as this copyright and license information must be included.

                History
                : 7 May 2021
                : 4 June 2021
                : 9 June 2021
                : 15 June 2021
                Categories
                Original Paper
                Original Paper

                response rates,electronic survey,cancer,covid-19,pandemic,surveillance,cancer patients,health promotion,digital health,patient experience,health outcomes

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