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Information-Seeking Strategies of People with Multiple Sclerosis in Spain: The INFOSEEK-MS Study
PURPOSE: Patients with multiple sclerosis (MS) are increasingly demanding access to reliable information regarding their disease. The objective of the INFOSEEK-MS study was to assess what are the strategies people with MS use when searching for information on their disease, including sources, freque...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762518/ https://www.ncbi.nlm.nih.gov/pubmed/35046641 http://dx.doi.org/10.2147/PPA.S344690 |
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author | Higueras, Yolanda Salas, Elisa Meca-Lallana, Virginia Carrascal Rueda, Pedro Rodríguez De la Fuente, Ofir Cabello-Moruno, Rosana Maurino, Jorge Ruiz Díaz, Miguel Ángel |
author_facet | Higueras, Yolanda Salas, Elisa Meca-Lallana, Virginia Carrascal Rueda, Pedro Rodríguez De la Fuente, Ofir Cabello-Moruno, Rosana Maurino, Jorge Ruiz Díaz, Miguel Ángel |
author_sort | Higueras, Yolanda |
collection | PubMed |
description | PURPOSE: Patients with multiple sclerosis (MS) are increasingly demanding access to reliable information regarding their disease. The objective of the INFOSEEK-MS study was to assess what are the strategies people with MS use when searching for information on their disease, including sources, frequency, reliability, and preferred content. PATIENTS AND METHODS: A non-interventional, cross-sectional study was conducted. Patients with a diagnosis of MS according to the 2010 McDonald criteria were included. The InfoSeek questionnaire was used to assess patients’ strategies when seeking information about the disease. Clinical characteristics and other variables, including disability, quality of life, fatigue, cognition, anxiety and depression, were analysed using the Expanded Disability Status Scale (EDSS), Multiple Sclerosis Impact Scale (MSIS-29), 5-item Modified Fatigue Scale (MFIS-5), Symbol Digit Modalities Test (SDMT), and Hospital Anxiety and Depression Scale (HADS), respectively. RESULTS: Three hundred and two patients were studied (mean age: 42.3 ± 10 years, 64% female, mean disease duration: 9.6 ± 7.0 years, 90% with relapsing-remitting MS, and mean EDSS score: 2.6 ± 1.9). The internet (either via mobile or computer) is a frequently reported source of information. Lifestyle-related information (67.2%), research and emerging treatments (63.6%), symptom control (49.7%), sharing experiences with other patients (46.4%), and disease prognosis (46.4%) were the most searched topics. Neurologists and nurses were the most trusted source of information. Younger patients and higher SDMT scores were associated with all search resources (M = 37.7 and M = 49.97, respectively). The frequency of searches was related to the number of relapses (R(2) = 0.07), EDSS (R(2) = 0.14), MSIS-29 physical and psychological components (R(2) = 0.132) and inversely with depression (R(2) = 0.132). CONCLUSION: Although healthcare professionals are considered the most reliable source of information for people with MS, searching for information on the Internet is very frequent. An individualized information strategy considering the different factors involved is needed. |
format | Online Article Text |
id | pubmed-8762518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-87625182022-01-18 Information-Seeking Strategies of People with Multiple Sclerosis in Spain: The INFOSEEK-MS Study Higueras, Yolanda Salas, Elisa Meca-Lallana, Virginia Carrascal Rueda, Pedro Rodríguez De la Fuente, Ofir Cabello-Moruno, Rosana Maurino, Jorge Ruiz Díaz, Miguel Ángel Patient Prefer Adherence Original Research PURPOSE: Patients with multiple sclerosis (MS) are increasingly demanding access to reliable information regarding their disease. The objective of the INFOSEEK-MS study was to assess what are the strategies people with MS use when searching for information on their disease, including sources, frequency, reliability, and preferred content. PATIENTS AND METHODS: A non-interventional, cross-sectional study was conducted. Patients with a diagnosis of MS according to the 2010 McDonald criteria were included. The InfoSeek questionnaire was used to assess patients’ strategies when seeking information about the disease. Clinical characteristics and other variables, including disability, quality of life, fatigue, cognition, anxiety and depression, were analysed using the Expanded Disability Status Scale (EDSS), Multiple Sclerosis Impact Scale (MSIS-29), 5-item Modified Fatigue Scale (MFIS-5), Symbol Digit Modalities Test (SDMT), and Hospital Anxiety and Depression Scale (HADS), respectively. RESULTS: Three hundred and two patients were studied (mean age: 42.3 ± 10 years, 64% female, mean disease duration: 9.6 ± 7.0 years, 90% with relapsing-remitting MS, and mean EDSS score: 2.6 ± 1.9). The internet (either via mobile or computer) is a frequently reported source of information. Lifestyle-related information (67.2%), research and emerging treatments (63.6%), symptom control (49.7%), sharing experiences with other patients (46.4%), and disease prognosis (46.4%) were the most searched topics. Neurologists and nurses were the most trusted source of information. Younger patients and higher SDMT scores were associated with all search resources (M = 37.7 and M = 49.97, respectively). The frequency of searches was related to the number of relapses (R(2) = 0.07), EDSS (R(2) = 0.14), MSIS-29 physical and psychological components (R(2) = 0.132) and inversely with depression (R(2) = 0.132). CONCLUSION: Although healthcare professionals are considered the most reliable source of information for people with MS, searching for information on the Internet is very frequent. An individualized information strategy considering the different factors involved is needed. Dove 2022-01-11 /pmc/articles/PMC8762518/ /pubmed/35046641 http://dx.doi.org/10.2147/PPA.S344690 Text en © 2022 Higueras et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Higueras, Yolanda Salas, Elisa Meca-Lallana, Virginia Carrascal Rueda, Pedro Rodríguez De la Fuente, Ofir Cabello-Moruno, Rosana Maurino, Jorge Ruiz Díaz, Miguel Ángel Information-Seeking Strategies of People with Multiple Sclerosis in Spain: The INFOSEEK-MS Study |
title | Information-Seeking Strategies of People with Multiple Sclerosis in Spain: The INFOSEEK-MS Study |
title_full | Information-Seeking Strategies of People with Multiple Sclerosis in Spain: The INFOSEEK-MS Study |
title_fullStr | Information-Seeking Strategies of People with Multiple Sclerosis in Spain: The INFOSEEK-MS Study |
title_full_unstemmed | Information-Seeking Strategies of People with Multiple Sclerosis in Spain: The INFOSEEK-MS Study |
title_short | Information-Seeking Strategies of People with Multiple Sclerosis in Spain: The INFOSEEK-MS Study |
title_sort | information-seeking strategies of people with multiple sclerosis in spain: the infoseek-ms study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762518/ https://www.ncbi.nlm.nih.gov/pubmed/35046641 http://dx.doi.org/10.2147/PPA.S344690 |
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