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Acceptability of self-sampling human papillomavirus test for cervical cancer screening in Japan: A questionnaire survey in the ACCESS trial
In terms of medical policy for cervical cancer prevention, Japan lags far behind other industrialized countries. We initiated a randomized controlled trial to evaluate the self-sampling human papillomavirus (HPV) test as a tool to raise screening uptake and detection of pre-cancer. This study was co...
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Published in: | PloS one 2023-06, Vol.18 (6), p.e0286909-e0286909 |
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creator | Fujita, Misuzu Nagashima, Kengo Shimazu, Minobu Suzuki, Misae Tauchi, Ichiro Sakuma, Miwa Yamamoto, Setsuko Hanaoka, Hideki Shozu, Makio Tsuruoka, Nobuhide Kasai, Tokuzo Hata, Akira |
description | In terms of medical policy for cervical cancer prevention, Japan lags far behind other industrialized countries. We initiated a randomized controlled trial to evaluate the self-sampling human papillomavirus (HPV) test as a tool to raise screening uptake and detection of pre-cancer. This study was conducted to explore the acceptability and preference of self-sampling using a subset of the data from this trial.
A pre-invitation letter was sent to eligible women, aged 30-59 years who had not undergone cervical cancer screening for three or more years. After excluding those who declined to participate in this trial, the remaining women were assigned to the self-sampling and control groups. A second invitation letter was sent to the former group, and those wanting to undergo the self-sampling test ordered the kit. A self-sampling HPV kit, consent form, and a self-administered questionnaire were sent to participants who ordered the test.
Of the 7,340 participants in the self-sampling group, 1,196 (16.3%) administered the test, and 1,192 (99.7%) answered the questionnaire. Acceptability of the test was favorable; 75.3-81.3% of participants agreed with positive impressions (easy, convenient, and clarity of instruction), and 65.1-77.8% disagreed with negative impressions (painful, uncomfortable, and embarrassing). However, only 21.2% were confident in their sampling procedure. Willingness to undergo screening with a self-collected sample was significantly higher than that with a doctor-collected sample (89.3% vs. 49.1%; p |
doi_str_mv | 10.1371/journal.pone.0286909 |
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A pre-invitation letter was sent to eligible women, aged 30-59 years who had not undergone cervical cancer screening for three or more years. After excluding those who declined to participate in this trial, the remaining women were assigned to the self-sampling and control groups. A second invitation letter was sent to the former group, and those wanting to undergo the self-sampling test ordered the kit. A self-sampling HPV kit, consent form, and a self-administered questionnaire were sent to participants who ordered the test.
Of the 7,340 participants in the self-sampling group, 1,196 (16.3%) administered the test, and 1,192 (99.7%) answered the questionnaire. Acceptability of the test was favorable; 75.3-81.3% of participants agreed with positive impressions (easy, convenient, and clarity of instruction), and 65.1-77.8% disagreed with negative impressions (painful, uncomfortable, and embarrassing). However, only 21.2% were confident in their sampling procedure. Willingness to undergo screening with a self-collected sample was significantly higher than that with a doctor-collected sample (89.3% vs. 49.1%; p<0.001). Willingness to undergo screening with a doctor-collected sample was inversely associated with age and duration without screening (both p<0.001), but that with a self-collected sample was not associated.
Among women who used the self-sampling HPV test, high acceptability was confirmed, while concerns about self-sampling procedures remained. Screening with a self-collected sample was preferred over a doctor-collected sample and the former might alleviate disparities in screening rates.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0286909</identifier><identifier>PMID: 37289798</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acceptability ; Access to information ; Biology and life sciences ; Cancer ; Cancer screening ; Care and treatment ; Cellular biology ; Cervical cancer ; Chi-square test ; Clinical trials ; Diagnosis ; Human papillomavirus ; Immunization ; Medical screening ; Medicine and Health Sciences ; Oncology, Experimental ; Papillomavirus infections ; Papillomaviruses ; People and Places ; Performance evaluation ; Physical Sciences ; Prevention ; Questionnaires ; Regression analysis ; Research and Analysis Methods ; Sampling ; Statistical analysis ; Surveys</subject><ispartof>PloS one, 2023-06, Vol.18 (6), p.e0286909-e0286909</ispartof><rights>Copyright: © 2023 Fujita et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</rights><rights>COPYRIGHT 2023 Public Library of Science</rights><rights>2023 Fujita et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 Fujita et al 2023 Fujita et al</rights><rights>2023 Fujita et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c693t-d755ab784b25832e580661eb99d818d279e29e2883cbaf6d8d66d3b7ac34976d3</citedby><cites>FETCH-LOGICAL-c693t-d755ab784b25832e580661eb99d818d279e29e2883cbaf6d8d66d3b7ac34976d3</cites><orcidid>0000-0001-5308-4744 ; 0000-0003-4529-9045 ; 0000-0002-7247-2205</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2823977395/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2823977395?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,36992,44569,53769,53771,74872</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37289798$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Du, Ruofei</contributor><creatorcontrib>Fujita, Misuzu</creatorcontrib><creatorcontrib>Nagashima, Kengo</creatorcontrib><creatorcontrib>Shimazu, Minobu</creatorcontrib><creatorcontrib>Suzuki, Misae</creatorcontrib><creatorcontrib>Tauchi, Ichiro</creatorcontrib><creatorcontrib>Sakuma, Miwa</creatorcontrib><creatorcontrib>Yamamoto, Setsuko</creatorcontrib><creatorcontrib>Hanaoka, Hideki</creatorcontrib><creatorcontrib>Shozu, Makio</creatorcontrib><creatorcontrib>Tsuruoka, Nobuhide</creatorcontrib><creatorcontrib>Kasai, Tokuzo</creatorcontrib><creatorcontrib>Hata, Akira</creatorcontrib><title>Acceptability of self-sampling human papillomavirus test for cervical cancer screening in Japan: A questionnaire survey in the ACCESS trial</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>In terms of medical policy for cervical cancer prevention, Japan lags far behind other industrialized countries. We initiated a randomized controlled trial to evaluate the self-sampling human papillomavirus (HPV) test as a tool to raise screening uptake and detection of pre-cancer. This study was conducted to explore the acceptability and preference of self-sampling using a subset of the data from this trial.
A pre-invitation letter was sent to eligible women, aged 30-59 years who had not undergone cervical cancer screening for three or more years. After excluding those who declined to participate in this trial, the remaining women were assigned to the self-sampling and control groups. A second invitation letter was sent to the former group, and those wanting to undergo the self-sampling test ordered the kit. A self-sampling HPV kit, consent form, and a self-administered questionnaire were sent to participants who ordered the test.
Of the 7,340 participants in the self-sampling group, 1,196 (16.3%) administered the test, and 1,192 (99.7%) answered the questionnaire. Acceptability of the test was favorable; 75.3-81.3% of participants agreed with positive impressions (easy, convenient, and clarity of instruction), and 65.1-77.8% disagreed with negative impressions (painful, uncomfortable, and embarrassing). However, only 21.2% were confident in their sampling procedure. Willingness to undergo screening with a self-collected sample was significantly higher than that with a doctor-collected sample (89.3% vs. 49.1%; p<0.001). Willingness to undergo screening with a doctor-collected sample was inversely associated with age and duration without screening (both p<0.001), but that with a self-collected sample was not associated.
Among women who used the self-sampling HPV test, high acceptability was confirmed, while concerns about self-sampling procedures remained. Screening with a self-collected sample was preferred over a doctor-collected sample and the former might alleviate disparities in screening rates.</description><subject>Acceptability</subject><subject>Access to information</subject><subject>Biology and life sciences</subject><subject>Cancer</subject><subject>Cancer screening</subject><subject>Care and treatment</subject><subject>Cellular biology</subject><subject>Cervical cancer</subject><subject>Chi-square test</subject><subject>Clinical trials</subject><subject>Diagnosis</subject><subject>Human papillomavirus</subject><subject>Immunization</subject><subject>Medical screening</subject><subject>Medicine and Health Sciences</subject><subject>Oncology, Experimental</subject><subject>Papillomavirus infections</subject><subject>Papillomaviruses</subject><subject>People and Places</subject><subject>Performance evaluation</subject><subject>Physical 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of self-sampling human papillomavirus test for cervical cancer screening in Japan: A questionnaire survey in the ACCESS trial</title><author>Fujita, Misuzu ; Nagashima, Kengo ; Shimazu, Minobu ; Suzuki, Misae ; Tauchi, Ichiro ; Sakuma, Miwa ; Yamamoto, Setsuko ; Hanaoka, Hideki ; Shozu, Makio ; Tsuruoka, Nobuhide ; Kasai, Tokuzo ; Hata, Akira</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c693t-d755ab784b25832e580661eb99d818d279e29e2883cbaf6d8d66d3b7ac34976d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acceptability</topic><topic>Access to information</topic><topic>Biology and life sciences</topic><topic>Cancer</topic><topic>Cancer screening</topic><topic>Care and treatment</topic><topic>Cellular biology</topic><topic>Cervical cancer</topic><topic>Chi-square test</topic><topic>Clinical trials</topic><topic>Diagnosis</topic><topic>Human 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Hideki</au><au>Shozu, Makio</au><au>Tsuruoka, Nobuhide</au><au>Kasai, Tokuzo</au><au>Hata, Akira</au><au>Du, Ruofei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acceptability of self-sampling human papillomavirus test for cervical cancer screening in Japan: A questionnaire survey in the ACCESS trial</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2023-06-08</date><risdate>2023</risdate><volume>18</volume><issue>6</issue><spage>e0286909</spage><epage>e0286909</epage><pages>e0286909-e0286909</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>In terms of medical policy for cervical cancer prevention, Japan lags far behind other industrialized countries. We initiated a randomized controlled trial to evaluate the self-sampling human papillomavirus (HPV) test as a tool to raise screening uptake and detection of pre-cancer. This study was conducted to explore the acceptability and preference of self-sampling using a subset of the data from this trial.
A pre-invitation letter was sent to eligible women, aged 30-59 years who had not undergone cervical cancer screening for three or more years. After excluding those who declined to participate in this trial, the remaining women were assigned to the self-sampling and control groups. A second invitation letter was sent to the former group, and those wanting to undergo the self-sampling test ordered the kit. A self-sampling HPV kit, consent form, and a self-administered questionnaire were sent to participants who ordered the test.
Of the 7,340 participants in the self-sampling group, 1,196 (16.3%) administered the test, and 1,192 (99.7%) answered the questionnaire. Acceptability of the test was favorable; 75.3-81.3% of participants agreed with positive impressions (easy, convenient, and clarity of instruction), and 65.1-77.8% disagreed with negative impressions (painful, uncomfortable, and embarrassing). However, only 21.2% were confident in their sampling procedure. Willingness to undergo screening with a self-collected sample was significantly higher than that with a doctor-collected sample (89.3% vs. 49.1%; p<0.001). Willingness to undergo screening with a doctor-collected sample was inversely associated with age and duration without screening (both p<0.001), but that with a self-collected sample was not associated.
Among women who used the self-sampling HPV test, high acceptability was confirmed, while concerns about self-sampling procedures remained. Screening with a self-collected sample was preferred over a doctor-collected sample and the former might alleviate disparities in screening rates.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>37289798</pmid><doi>10.1371/journal.pone.0286909</doi><tpages>e0286909</tpages><orcidid>https://orcid.org/0000-0001-5308-4744</orcidid><orcidid>https://orcid.org/0000-0003-4529-9045</orcidid><orcidid>https://orcid.org/0000-0002-7247-2205</orcidid><oa>free_for_read</oa></addata></record> |
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identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2023-06, Vol.18 (6), p.e0286909-e0286909 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_2823977395 |
source | Publicly Available Content Database; PubMed Central |
subjects | Acceptability Access to information Biology and life sciences Cancer Cancer screening Care and treatment Cellular biology Cervical cancer Chi-square test Clinical trials Diagnosis Human papillomavirus Immunization Medical screening Medicine and Health Sciences Oncology, Experimental Papillomavirus infections Papillomaviruses People and Places Performance evaluation Physical Sciences Prevention Questionnaires Regression analysis Research and Analysis Methods Sampling Statistical analysis Surveys |
title | Acceptability of self-sampling human papillomavirus test for cervical cancer screening in Japan: A questionnaire survey in the ACCESS trial |
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