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Applying citizen science to engage families affected by ovarian cancer in developing genetic service outreach strategies

Citizen science (CS) approaches involving non-professional researchers (citizens) as research collaborators has been used infrequently in health promotion generally and specifically, in cancer prevention. Standardized CS approaches may be especially useful for developing communication interventions...

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Autores principales: McBride, Colleen M., Campbell, Gavin P., Zhao, Jingsong, Pentz, Rebecca D., Escoffery, Cam, Komonos, Michael, Cannova, Kelly, Byrne, Janice L. B., Paris, Nancy M., Shepperd, James R., Guan, Yue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8843236/
https://www.ncbi.nlm.nih.gov/pubmed/35157722
http://dx.doi.org/10.1371/journal.pone.0262575
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author McBride, Colleen M.
Campbell, Gavin P.
Zhao, Jingsong
Pentz, Rebecca D.
Escoffery, Cam
Komonos, Michael
Cannova, Kelly
Byrne, Janice L. B.
Paris, Nancy M.
Shepperd, James R.
Guan, Yue
author_facet McBride, Colleen M.
Campbell, Gavin P.
Zhao, Jingsong
Pentz, Rebecca D.
Escoffery, Cam
Komonos, Michael
Cannova, Kelly
Byrne, Janice L. B.
Paris, Nancy M.
Shepperd, James R.
Guan, Yue
author_sort McBride, Colleen M.
collection PubMed
description Citizen science (CS) approaches involving non-professional researchers (citizens) as research collaborators has been used infrequently in health promotion generally and specifically, in cancer prevention. Standardized CS approaches may be especially useful for developing communication interventions to encourage families to consider cancer genetic services. We engaged survivors of ovarian cancer and their close relatives as CS collaborators to collect and help interpret data to inform content for a website, printed invitation materials, and short-message reminders. We applied an implementation quality framework, and posed four research questions regarding the feasibility of CS: recruitment, data collection, data quality and evaluation of the experience. CS members were recruited through three networks: clinical sites, local and national cancer support organizations, and online ovarian cancer patient support groups. The professional research team operationalized theory-aligned CS tasks, five data collection options, question banks/scripts for creating surveys, structured interviews, online training and ongoing support from research coaches. 14 CS members agreed to the 12-week and 20-hour commitment for an honorarium. CS members opted to do both qualitative and quantitative assessments. CS members collected 261 surveys and 39 structured interviews. The largest number of surveys were collected for Task 1 (n = 102) to assess survivors’ reactions to different possible options for motivating survivors to visit a study website; 77% of this data were complete (i.e., no missing values). Data collected for tasks 2, 3, 4, and 5 (e.g., assessment of survivors’ and relatives’ respective communication preferences) ranged from 10 to 58 surveys (80% to 84% completeness). All data were collected within the specified time frame. CSs reported 17 hours of work on average and regarded the experience positively. Our experience suggests that CS engagement is feasible, can yield comprehensive quantitative and qualitative data, and is achievable in a relatively a short timeline.
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spelling pubmed-88432362022-02-15 Applying citizen science to engage families affected by ovarian cancer in developing genetic service outreach strategies McBride, Colleen M. Campbell, Gavin P. Zhao, Jingsong Pentz, Rebecca D. Escoffery, Cam Komonos, Michael Cannova, Kelly Byrne, Janice L. B. Paris, Nancy M. Shepperd, James R. Guan, Yue PLoS One Research Article Citizen science (CS) approaches involving non-professional researchers (citizens) as research collaborators has been used infrequently in health promotion generally and specifically, in cancer prevention. Standardized CS approaches may be especially useful for developing communication interventions to encourage families to consider cancer genetic services. We engaged survivors of ovarian cancer and their close relatives as CS collaborators to collect and help interpret data to inform content for a website, printed invitation materials, and short-message reminders. We applied an implementation quality framework, and posed four research questions regarding the feasibility of CS: recruitment, data collection, data quality and evaluation of the experience. CS members were recruited through three networks: clinical sites, local and national cancer support organizations, and online ovarian cancer patient support groups. The professional research team operationalized theory-aligned CS tasks, five data collection options, question banks/scripts for creating surveys, structured interviews, online training and ongoing support from research coaches. 14 CS members agreed to the 12-week and 20-hour commitment for an honorarium. CS members opted to do both qualitative and quantitative assessments. CS members collected 261 surveys and 39 structured interviews. The largest number of surveys were collected for Task 1 (n = 102) to assess survivors’ reactions to different possible options for motivating survivors to visit a study website; 77% of this data were complete (i.e., no missing values). Data collected for tasks 2, 3, 4, and 5 (e.g., assessment of survivors’ and relatives’ respective communication preferences) ranged from 10 to 58 surveys (80% to 84% completeness). All data were collected within the specified time frame. CSs reported 17 hours of work on average and regarded the experience positively. Our experience suggests that CS engagement is feasible, can yield comprehensive quantitative and qualitative data, and is achievable in a relatively a short timeline. Public Library of Science 2022-02-14 /pmc/articles/PMC8843236/ /pubmed/35157722 http://dx.doi.org/10.1371/journal.pone.0262575 Text en © 2022 McBride et al https://creativecommons.org/licenses/by/4.0/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 author and source are credited.
spellingShingle Research Article
McBride, Colleen M.
Campbell, Gavin P.
Zhao, Jingsong
Pentz, Rebecca D.
Escoffery, Cam
Komonos, Michael
Cannova, Kelly
Byrne, Janice L. B.
Paris, Nancy M.
Shepperd, James R.
Guan, Yue
Applying citizen science to engage families affected by ovarian cancer in developing genetic service outreach strategies
title Applying citizen science to engage families affected by ovarian cancer in developing genetic service outreach strategies
title_full Applying citizen science to engage families affected by ovarian cancer in developing genetic service outreach strategies
title_fullStr Applying citizen science to engage families affected by ovarian cancer in developing genetic service outreach strategies
title_full_unstemmed Applying citizen science to engage families affected by ovarian cancer in developing genetic service outreach strategies
title_short Applying citizen science to engage families affected by ovarian cancer in developing genetic service outreach strategies
title_sort applying citizen science to engage families affected by ovarian cancer in developing genetic service outreach strategies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8843236/
https://www.ncbi.nlm.nih.gov/pubmed/35157722
http://dx.doi.org/10.1371/journal.pone.0262575
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