Development and content validation of the information assessment method for patients and consumers
Online consumer health information addresses health problems, self-care, disease prevention, and health care services and is intended for the general public. Using this information, people can improve their knowledge, participation in health decision-making, and health. However, there are no compreh...
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Published in: | JMIR research protocols Vol. 3; no. 1; p. e7 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
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Gunther Eysenbach MD MPH, Associate Professor
01-01-2014
JMIR Publications JMIR Publications Inc |
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Abstract | Online consumer health information addresses health problems, self-care, disease prevention, and health care services and is intended for the general public. Using this information, people can improve their knowledge, participation in health decision-making, and health. However, there are no comprehensive instruments to evaluate the value of health information from a consumer perspective.
We collaborated with information providers to develop and validate the Information Assessment Method for all (IAM4all) that can be used to collect feedback from information consumers (including patients), and to enable a two-way knowledge translation between information providers and consumers.
Content validation steps were followed to develop the IAM4all questionnaire. The first version was based on a theoretical framework from information science, a critical literature review and prior work. Then, 16 laypersons were interviewed on their experience with online health information and specifically their impression of the IAM4all questionnaire. Based on the summaries and interpretations of interviews, questionnaire items were revised, added, and excluded, thus creating the second version of the questionnaire. Subsequently, a panel of 12 information specialists and 8 health researchers participated in an online survey to rate each questionnaire item for relevance, clarity, representativeness, and specificity. The result of this expert panel contributed to the third, current, version of the questionnaire.
The current version of the IAM4all questionnaire is structured by four levels of outcomes of information seeking/receiving: situational relevance, cognitive impact, information use, and health benefits. Following the interviews and the expert panel survey, 9 questionnaire items were confirmed as relevant, clear, representative, and specific. To improve readability and accessibility for users with a lower level of literacy, 19 items were reworded and all inconsistencies in using a passive or active voice have been solved. One item was removed due to redundancy. The current version of the IAM4all questionnaire contains 28 items.
We developed and content validated the IAM4all in partnership with information providers, information specialists, researchers and representatives of information consumers. This questionnaire can be integrated within electronic knowledge resources to stimulate users' reflection (eg, their intention to use information). We claim that any organization (eg, publishers, community organizations, or patient associations), can evaluate and improve their online consumer health information from a consumers' perspective using this method. |
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AbstractList | Background: Online consumer health information addresses health problems, self-care, disease prevention, and health care services and is intended for the general public. Using this information, people can improve their knowledge, participation in health decision-making, and health. However, there are no comprehensive instruments to evaluate the value of health information from a consumer perspective. Objective: We collaborated with information providers to develop and validate the Information Assessment Method for all (IAM4all) that can be used to collect feedback from information consumers (including patients), and to enable a two-way knowledge translation between information providers and consumers. Methods: Content validation steps were followed to develop the IAM4all questionnaire. The first version was based on a theoretical framework from information science, a critical literature review and prior work. Then, 16 laypersons were interviewed on their experience with online health information and specifically their impression of the IAM4all questionnaire. Based on the summaries and interpretations of interviews, questionnaire items were revised, added, and excluded, thus creating the second version of the questionnaire. Subsequently, a panel of 12 information specialists and 8 health researchers participated in an online survey to rate each questionnaire item for relevance, clarity, representativeness, and specificity. The result of this expert panel contributed to the third, current, version of the questionnaire. Results: The current version of the IAM4all questionnaire is structured by four levels of outcomes of information seeking/receiving: situational relevance, cognitive impact, information use, and health benefits. Following the interviews and the expert panel survey, 9 questionnaire items were confirmed as relevant, clear, representative, and specific. To improve readability and accessibility for users with a lower level of literacy, 19 items were reworded and all inconsistencies in using a passive or active voice have been solved. One item was removed due to redundancy. The current version of the IAM4all questionnaire contains 28 items. Conclusions: We developed and content validated the IAM4all in partnership with information providers, information specialists, researchers and representatives of information consumers. This questionnaire can be integrated within electronic knowledge resources to stimulate users’ reflection (eg, their intention to use information). We claim that any organization (eg, publishers, community organizations, or patient associations), can evaluate and improve their online consumer health information from a consumers’ perspective using this method. BACKGROUNDOnline consumer health information addresses health problems, self-care, disease prevention, and health care services and is intended for the general public. Using this information, people can improve their knowledge, participation in health decision-making, and health. However, there are no comprehensive instruments to evaluate the value of health information from a consumer perspective.OBJECTIVEWe collaborated with information providers to develop and validate the Information Assessment Method for all (IAM4all) that can be used to collect feedback from information consumers (including patients), and to enable a two-way knowledge translation between information providers and consumers.METHODSContent validation steps were followed to develop the IAM4all questionnaire. The first version was based on a theoretical framework from information science, a critical literature review and prior work. Then, 16 laypersons were interviewed on their experience with online health information and specifically their impression of the IAM4all questionnaire. Based on the summaries and interpretations of interviews, questionnaire items were revised, added, and excluded, thus creating the second version of the questionnaire. Subsequently, a panel of 12 information specialists and 8 health researchers participated in an online survey to rate each questionnaire item for relevance, clarity, representativeness, and specificity. The result of this expert panel contributed to the third, current, version of the questionnaire.RESULTSThe current version of the IAM4all questionnaire is structured by four levels of outcomes of information seeking/receiving: situational relevance, cognitive impact, information use, and health benefits. Following the interviews and the expert panel survey, 9 questionnaire items were confirmed as relevant, clear, representative, and specific. To improve readability and accessibility for users with a lower level of literacy, 19 items were reworded and all inconsistencies in using a passive or active voice have been solved. One item was removed due to redundancy. The current version of the IAM4all questionnaire contains 28 items.CONCLUSIONSWe developed and content validated the IAM4all in partnership with information providers, information specialists, researchers and representatives of information consumers. This questionnaire can be integrated within electronic knowledge resources to stimulate users' reflection (eg, their intention to use information). We claim that any organization (eg, publishers, community organizations, or patient associations), can evaluate and improve their online consumer health information from a consumers' perspective using this method. Online consumer health information addresses health problems, self-care, disease prevention, and health care services and is intended for the general public. Using this information, people can improve their knowledge, participation in health decision-making, and health. However, there are no comprehensive instruments to evaluate the value of health information from a consumer perspective. We collaborated with information providers to develop and validate the Information Assessment Method for all (IAM4all) that can be used to collect feedback from information consumers (including patients), and to enable a two-way knowledge translation between information providers and consumers. We developed and content validated the IAM4all in partnership with information providers, information specialists, researchers and representatives of information consumers. This questionnaire can be integrated within electronic knowledge resources to stimulate usersʼ reflection (eg, their intention to use information). We claim that any organization (eg, publishers, community organizations, or patient associations), can evaluate and improve their online consumer health information from a consumersʼ perspective using this method. Online consumer health information addresses health problems, self-care, disease prevention, and health care services and is intended for the general public. Using this information, people can improve their knowledge, participation in health decision-making, and health. However, there are no comprehensive instruments to evaluate the value of health information from a consumer perspective. We collaborated with information providers to develop and validate the Information Assessment Method for all (IAM4all) that can be used to collect feedback from information consumers (including patients), and to enable a two-way knowledge translation between information providers and consumers. Content validation steps were followed to develop the IAM4all questionnaire. The first version was based on a theoretical framework from information science, a critical literature review and prior work. Then, 16 laypersons were interviewed on their experience with online health information and specifically their impression of the IAM4all questionnaire. Based on the summaries and interpretations of interviews, questionnaire items were revised, added, and excluded, thus creating the second version of the questionnaire. Subsequently, a panel of 12 information specialists and 8 health researchers participated in an online survey to rate each questionnaire item for relevance, clarity, representativeness, and specificity. The result of this expert panel contributed to the third, current, version of the questionnaire. The current version of the IAM4all questionnaire is structured by four levels of outcomes of information seeking/receiving: situational relevance, cognitive impact, information use, and health benefits. Following the interviews and the expert panel survey, 9 questionnaire items were confirmed as relevant, clear, representative, and specific. To improve readability and accessibility for users with a lower level of literacy, 19 items were reworded and all inconsistencies in using a passive or active voice have been solved. One item was removed due to redundancy. The current version of the IAM4all questionnaire contains 28 items. We developed and content validated the IAM4all in partnership with information providers, information specialists, researchers and representatives of information consumers. This questionnaire can be integrated within electronic knowledge resources to stimulate users' reflection (eg, their intention to use information). We claim that any organization (eg, publishers, community organizations, or patient associations), can evaluate and improve their online consumer health information from a consumers' perspective using this method. |
Author | Tang, David L Boruff, Jill Lagarde, François Shohet, Linda Pluye, Pierre Légaré, France Shulha, Michael Barbosa Galvão, Maria Cristiane Ricarte, Ivan Lm Rosenberg, Ellen Hutsul, Jo-Anne Repchinsky, Carol A Grad, Roland M Dunikowski, Lynn Kloda, Lorie Frati, Francesca Doray, Geneviève Burnand, Bernard Bartlett, Gillian Johnson-Lafleur, Janique Macaulay, Ann Stephenson, Randolph Murray, Susan Granikov, Vera |
AuthorAffiliation | 5 Department of Psychology Université du Québec à Montréal (UQAM) Montreal, QC Canada 9 Department of Family Medicine and Emergency Medicine Université Laval Quebec, QC Canada 12 Health Sciences Library Jewish General Hospital Montreal, QC Canada 8 Institute of social and preventive medicine Lausanne University Hospital Lausanne Switzerland 11 Life Sciences Library McGill University Montreal, QC Canada 13 Lucie and André Chagnon Foundation Montreal, QC Canada 6 The Centre for Literacy Quebec Montreal, QC Canada 2 Information Technology Primary Care Research Group Department of Family Medicine McGill University Montreal, QC Canada 1 Department of Family Medicine McGill University Montreal, QC Canada 3 Department of Social Medicine Faculty of Medicine of Ribeirao Preto University of Sao Paulo Sao Paulo Brazil 7 Canadian Pharmacists Association Ottawa, ON Canada 4 School of Electrical and Computer Engineering University of Campinas - UNICAMP Campinas Brazil 10 Library Services College of Family Physi |
AuthorAffiliation_xml | – name: 6 The Centre for Literacy Quebec Montreal, QC Canada – name: 4 School of Electrical and Computer Engineering University of Campinas - UNICAMP Campinas Brazil – name: 13 Lucie and André Chagnon Foundation Montreal, QC Canada – name: 10 Library Services College of Family Physicians of Canada London, ON Canada – name: 3 Department of Social Medicine Faculty of Medicine of Ribeirao Preto University of Sao Paulo Sao Paulo Brazil – name: 5 Department of Psychology Université du Québec à Montréal (UQAM) Montreal, QC Canada – name: 11 Life Sciences Library McGill University Montreal, QC Canada – name: 8 Institute of social and preventive medicine Lausanne University Hospital Lausanne Switzerland – name: 1 Department of Family Medicine McGill University Montreal, QC Canada – name: 2 Information Technology Primary Care Research Group Department of Family Medicine McGill University Montreal, QC Canada – name: 12 Health Sciences Library Jewish General Hospital Montreal, QC Canada – name: 7 Canadian Pharmacists Association Ottawa, ON Canada – name: 9 Department of Family Medicine and Emergency Medicine Université Laval Quebec, QC Canada |
Author_xml | – sequence: 1 givenname: Pierre surname: Pluye fullname: Pluye, Pierre email: pierre.pluye@mcgill.ca organization: Department of Family Medicine, McGill University, Montreal, QC, Canada. pierre.pluye@mcgill.ca – sequence: 2 givenname: Vera surname: Granikov fullname: Granikov, Vera – sequence: 3 givenname: Gillian surname: Bartlett fullname: Bartlett, Gillian – sequence: 4 givenname: Roland M surname: Grad fullname: Grad, Roland M – sequence: 5 givenname: David L surname: Tang fullname: Tang, David L – sequence: 6 givenname: Janique surname: Johnson-Lafleur fullname: Johnson-Lafleur, Janique – sequence: 7 givenname: Michael surname: Shulha fullname: Shulha, Michael – sequence: 8 givenname: Maria Cristiane surname: Barbosa Galvão fullname: Barbosa Galvão, Maria Cristiane – sequence: 9 givenname: Ivan Lm surname: Ricarte fullname: Ricarte, Ivan Lm – sequence: 10 givenname: Randolph surname: Stephenson fullname: Stephenson, Randolph – sequence: 11 givenname: Linda surname: Shohet fullname: Shohet, Linda – sequence: 12 givenname: Jo-Anne surname: Hutsul fullname: Hutsul, Jo-Anne – sequence: 13 givenname: Carol A surname: Repchinsky fullname: Repchinsky, Carol A – sequence: 14 givenname: Ellen surname: Rosenberg fullname: Rosenberg, Ellen – sequence: 15 givenname: Bernard surname: Burnand fullname: Burnand, Bernard – sequence: 16 givenname: France surname: Légaré fullname: Légaré, France – sequence: 17 givenname: Lynn surname: Dunikowski fullname: Dunikowski, Lynn – sequence: 18 givenname: Susan surname: Murray fullname: Murray, Susan – sequence: 19 givenname: Jill surname: Boruff fullname: Boruff, Jill – sequence: 20 givenname: Francesca surname: Frati fullname: Frati, Francesca – sequence: 21 givenname: Lorie surname: Kloda fullname: Kloda, Lorie – sequence: 22 givenname: Ann surname: Macaulay fullname: Macaulay, Ann – sequence: 23 givenname: François surname: Lagarde fullname: Lagarde, François – sequence: 24 givenname: Geneviève surname: Doray fullname: Doray, Geneviève |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24550180$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | 2014. This work is licensed under http://creativecommons.org/licenses/by/2.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. Pierre Pluye, Vera Granikov, Gillian Bartlett, Roland M. Grad, David L. Tang, Janique Johnson-Lafleur, Michael Shulha, Maria Cristiane Barbosa Galvão, Ivan LM Ricarte, Randolph Stephenson, Linda Shohet, Jo-Anne Hutsul, Carol A. Repchinsky, Ellen Rosenberg, Bernard Burnand, France Légaré, Lynn Dunikowski, Susan Murray, Jill Boruff, Francesca Frati, Lorie Kloda, Ann Macaulay, François Lagarde, Geneviève Doray. Originally published in JMIR Research Protocols (http://www.researchprotocols.org), 18.02.2014. 2014 |
Copyright_xml | – notice: 2014. This work is licensed under http://creativecommons.org/licenses/by/2.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. – notice: Pierre Pluye, Vera Granikov, Gillian Bartlett, Roland M. Grad, David L. Tang, Janique Johnson-Lafleur, Michael Shulha, Maria Cristiane Barbosa Galvão, Ivan LM Ricarte, Randolph Stephenson, Linda Shohet, Jo-Anne Hutsul, Carol A. Repchinsky, Ellen Rosenberg, Bernard Burnand, France Légaré, Lynn Dunikowski, Susan Murray, Jill Boruff, Francesca Frati, Lorie Kloda, Ann Macaulay, François Lagarde, Geneviève Doray. Originally published in JMIR Research Protocols (http://www.researchprotocols.org), 18.02.2014. 2014 |
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Keywords | content validity push technology information use consumer health information consumer-centered outcomes information retrieval |
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Title | Development and content validation of the information assessment method for patients and consumers |
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