Health literacy and information needs among German skin cancer patients in comparison to people without skin cancer: A survey

Author:

Hoffmann Julia1ORCID,Steeb Theresa23ORCID,Weber Christiane4,Doppler Astrid5,Schmitt Jochen1,Schadendorf Dirk6ORCID,Berking Carola12,Meier Friedegund78

Affiliation:

1. Zentrum für Evidenzbasierte Gesundheitsversorgung Universitätsklinikum Dresden Dresden Germany

2. Hautklinik, Universitätsklinikum Erlangen Friedrich‐Alexander‐Universität Erlangen‐Nürnberg Erlangen Germany

3. Comprehensive Cancer Center Erlangen–European metropolitan region Nürnberg (CCC ER‐EMN) Erlangen Germany

4. MEDEA GmbH Hamburg Germany

5. Melanom Info Deutschland (MID) e.V. Germany

6. Klinik für Dermatologie, Venerologie und Allergologie Universitätsklinikum Essen Essen Germany

7. Hauttumorzentrum am Universitätskrebszentrum und Nationalem Centrum für Tumorerkrankungen Dresden Dresden Germany

8. Klinik und Poliklinik für Dermatologie Universitätsklinikum Carl Gustav Carus an der Technischen Universität Dresden Dresden Germany

Abstract

AbstractBackgroundAn increasing number of patients are seeking health information on the internet. Health literacy and the quality of information are crucial to enable patients to find relevant high‐quality information.ObjectivesTo investigate the relevance of quality criteria for health information and to determine the health literacy of skin cancer patients (SC) in comparison to those without skin cancer (NSC).MethodsBetween December 2021 until February 2022 we undertook an online survey on the importance of multiple criteria to investigate the relevance of quality criteria of online health information. SC and NSC were eligible for participation. The questionnaire assessed participants´ health information‐seeking behavior and the evaluation of relevance of quality criteria for health information on a 5‐point‐LIKERT‐Scale. The participants´ health literacy was measured according to the health literacy measurement scale ranging from 0‐100. Comparisons between SC and NSC were investigated with t‐tests.ResultsWe retrieved data from 268 participants, of whom 98 (38%) were SC. Participants assigned the highest relevance to the health information topics treatment (4.7 ± 0.64) and effects of a disease (4.49 ± 0.76). Participants ranked the content of information with a mean of 4.72 (±0.57) to be the most relevant criterion, followed by objectivity (4.61 ± 0.67) and completeness of the information (4.59 ± 0.61). Participants showed the highest competence in understanding of information (62.4 ± 22.5) and in disease prevention (58.32 ± 22.9). They reached low values in accessing health related information (46.78 ± 25.62) and appraising it (33.16 ± 20.11). Subgroup analysis indicated that SC had a greater need for practical information that is helpful in dealing with a disease compared to NSC. They showed significantly lower health literacy than NSC.ConclusionsOur study documents that SC and NSC have a high need for different dimensions of quality of health information. These differences in the importance of criteria should be considered in the development of future targeted health information.

Funder

Nationale Versorgungskonferenz Hautkrebs

Publisher

Wiley

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