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Measuring the success of blinding in placebo-controlled trials: Should we be so quick to dismiss it?
What's new•Blinding in clinical trials has the potential to reduce bias.•There is a live yet underreported debate about the value of measuring blinding success.•Interpreting the success of blinding can be problematic and potentially misleading.•However, failure to report the success of blinding...
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Published in: | Journal of clinical epidemiology 2021-07, Vol.135, p.176-181 |
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container_title | Journal of clinical epidemiology |
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creator | Webster, Rebecca K. Bishop, Felicity Collins, Gary S. Evers, Andrea W.M. Hoffmann, Tammy Knottnerus, J. André Lamb, Sarah E. Macdonald, Helen Madigan, Claire Napadow, Vitaly Price, Amy Rees, Jonathan L. Howick, Jeremy |
description | What's new•Blinding in clinical trials has the potential to reduce bias.•There is a live yet underreported debate about the value of measuring blinding success.•Interpreting the success of blinding can be problematic and potentially misleading.•However, failure to report the success of blinding, if it is measured, seems like willful withholding of information that is at least potentially useful.•We suggest a middle road whereby the success of blinding be measured (where feasible) and interpreted with caution.
‘Blinding’ involves concealing knowledge of which trial participants received the interventions from participants themselves and other trial personnel throughout the trial. Blinding reduces bias arising from the beliefs and expectations of these groups. It is agreed that where possible, blinding should be attempted, for example by ensuring that experimental and control treatments look the same. However, there is a debate about if we should measure whether blinding has been successful, this manuscript will discuss this controversy, including the benefits and risks of measuring blinding within the randomised controlled trial. |
doi_str_mv | 10.1016/j.jclinepi.2021.02.022 |
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‘Blinding’ involves concealing knowledge of which trial participants received the interventions from participants themselves and other trial personnel throughout the trial. Blinding reduces bias arising from the beliefs and expectations of these groups. It is agreed that where possible, blinding should be attempted, for example by ensuring that experimental and control treatments look the same. However, there is a debate about if we should measure whether blinding has been successful, this manuscript will discuss this controversy, including the benefits and risks of measuring blinding within the randomised controlled trial.</description><identifier>ISSN: 0895-4356</identifier><identifier>EISSN: 1878-5921</identifier><identifier>DOI: 10.1016/j.jclinepi.2021.02.022</identifier><identifier>PMID: 33662512</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Blinding ; Clinical trials ; Clinical Trials as Topic - methods ; Double-Blind Method ; Epidemiology ; Humans ; Intervention ; Masking ; Measuring ; Placebo Effect ; Placebos ; Reporting guidelines ; Research Design ; Single-Blind Method ; Stroke ; Success ; Trials ; Vitamin C</subject><ispartof>Journal of clinical epidemiology, 2021-07, Vol.135, p.176-181</ispartof><rights>2021 Elsevier Inc.</rights><rights>Copyright © 2021 Elsevier Inc. All rights reserved.</rights><rights>2021. Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c444t-221d8cde59b4ae4db0cd28abfdee5c08eb43ac08813e351cbe923ad459e813fb3</citedby><cites>FETCH-LOGICAL-c444t-221d8cde59b4ae4db0cd28abfdee5c08eb43ac08813e351cbe923ad459e813fb3</cites><orcidid>0000-0002-8737-6662 ; 0000-0002-6782-0017 ; 0000-0002-5136-1098 ; 0000-0002-2772-2316 ; 0000-0002-0090-5091 ; 0000-0003-4349-7195 ; 0000-0001-5210-8548</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33662512$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Webster, Rebecca K.</creatorcontrib><creatorcontrib>Bishop, Felicity</creatorcontrib><creatorcontrib>Collins, Gary S.</creatorcontrib><creatorcontrib>Evers, Andrea W.M.</creatorcontrib><creatorcontrib>Hoffmann, Tammy</creatorcontrib><creatorcontrib>Knottnerus, J. André</creatorcontrib><creatorcontrib>Lamb, Sarah E.</creatorcontrib><creatorcontrib>Macdonald, Helen</creatorcontrib><creatorcontrib>Madigan, Claire</creatorcontrib><creatorcontrib>Napadow, Vitaly</creatorcontrib><creatorcontrib>Price, Amy</creatorcontrib><creatorcontrib>Rees, Jonathan L.</creatorcontrib><creatorcontrib>Howick, Jeremy</creatorcontrib><title>Measuring the success of blinding in placebo-controlled trials: Should we be so quick to dismiss it?</title><title>Journal of clinical epidemiology</title><addtitle>J Clin Epidemiol</addtitle><description>What's new•Blinding in clinical trials has the potential to reduce bias.•There is a live yet underreported debate about the value of measuring blinding success.•Interpreting the success of blinding can be problematic and potentially misleading.•However, failure to report the success of blinding, if it is measured, seems like willful withholding of information that is at least potentially useful.•We suggest a middle road whereby the success of blinding be measured (where feasible) and interpreted with caution.
‘Blinding’ involves concealing knowledge of which trial participants received the interventions from participants themselves and other trial personnel throughout the trial. Blinding reduces bias arising from the beliefs and expectations of these groups. It is agreed that where possible, blinding should be attempted, for example by ensuring that experimental and control treatments look the same. However, there is a debate about if we should measure whether blinding has been successful, this manuscript will discuss this controversy, including the benefits and risks of measuring blinding within the randomised controlled trial.</description><subject>Blinding</subject><subject>Clinical trials</subject><subject>Clinical Trials as Topic - methods</subject><subject>Double-Blind Method</subject><subject>Epidemiology</subject><subject>Humans</subject><subject>Intervention</subject><subject>Masking</subject><subject>Measuring</subject><subject>Placebo Effect</subject><subject>Placebos</subject><subject>Reporting guidelines</subject><subject>Research Design</subject><subject>Single-Blind Method</subject><subject>Stroke</subject><subject>Success</subject><subject>Trials</subject><subject>Vitamin C</subject><issn>0895-4356</issn><issn>1878-5921</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkUlrG0EQhZsQE8lK_oJoyCWXkXudJZfEGC8BGx_snJteaqKejKbl7hkb_3u3kJRDLoaCguJ7r4p6CC0pWVFCy7Nu1dneD7D1K0YYXRGWi31Ac1pXdSEbRj-iOakbWQguyxk6TakjhFakkp_QjPOyZJKyOXJ3oNMU_fAHj2vAabIWUsKhxSbbu93cD3jbawsmFDYMYwx9Dw6P0es-fccP6zD1Dr8ANlke8NPk7V88Bux82vhs5ccfn9FJm2H4cugL9Pvq8vHipri9v_51cX5bWCHEWDBGXW0dyMYIDcIZYh2rtWkdgLSkBiO4zr2mHLik1kDDuHZCNpBHreEL9G3vu43haYI0qnyBhb7XA4QpKSaaWpKKcJrRr_-hXZjikK9TTErJWSWozFS5p2wMKUVo1Tb6jY6vihK1y0F16piD2uWgCMvFsnB5sJ_MBtw_2fHxGfi5ByD_49lDVMl6GCw4H8GOygX_3o43fNGdXg</recordid><startdate>202107</startdate><enddate>202107</enddate><creator>Webster, Rebecca K.</creator><creator>Bishop, Felicity</creator><creator>Collins, Gary S.</creator><creator>Evers, Andrea W.M.</creator><creator>Hoffmann, Tammy</creator><creator>Knottnerus, J. André</creator><creator>Lamb, Sarah E.</creator><creator>Macdonald, Helen</creator><creator>Madigan, Claire</creator><creator>Napadow, Vitaly</creator><creator>Price, Amy</creator><creator>Rees, Jonathan L.</creator><creator>Howick, Jeremy</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7QP</scope><scope>7RV</scope><scope>7T2</scope><scope>7T7</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8737-6662</orcidid><orcidid>https://orcid.org/0000-0002-6782-0017</orcidid><orcidid>https://orcid.org/0000-0002-5136-1098</orcidid><orcidid>https://orcid.org/0000-0002-2772-2316</orcidid><orcidid>https://orcid.org/0000-0002-0090-5091</orcidid><orcidid>https://orcid.org/0000-0003-4349-7195</orcidid><orcidid>https://orcid.org/0000-0001-5210-8548</orcidid></search><sort><creationdate>202107</creationdate><title>Measuring the success of blinding in placebo-controlled trials: Should we be so quick to dismiss it?</title><author>Webster, Rebecca K. ; Bishop, Felicity ; Collins, Gary S. ; Evers, Andrea W.M. ; Hoffmann, Tammy ; Knottnerus, J. 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subjects | Blinding Clinical trials Clinical Trials as Topic - methods Double-Blind Method Epidemiology Humans Intervention Masking Measuring Placebo Effect Placebos Reporting guidelines Research Design Single-Blind Method Stroke Success Trials Vitamin C |
title | Measuring the success of blinding in placebo-controlled trials: Should we be so quick to dismiss it? |
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