Literature DB >> 17699171

Consent bias in research: how to avoid it.

Cornelia Junghans, Melvyn Jones.   

Abstract

Mesh：

Year:  2007        PMID： 17699171      PMCID： PMC1955004          DOI： 10.1136/hrt.2007.120113

Source DB:  PubMed          Journal:  Heart        ISSN： 1355-6037            Impact factor:   5.994


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  12 in total

1.  Recruiting patients to medical research: double blind randomised trial of "opt-in" versus "opt-out" strategies.

Authors:  Cornelia Junghans; Gene Feder; Harry Hemingway; Adam Timmis; Melvyn Jones
Journal:  BMJ       Date:  2005-09-12

2.  A method to determine if consenters to population surveys are representative of the target study population.

Authors:  Helen F Boardman; Elaine Thomas; Helen Ogden; David S Millson; Peter R Croft
Journal:  J Public Health (Oxf)       Date:  2005-03-17       Impact factor: 2.341

3.  Ethics and research governance in a multicentre study: add 150 days to your study protocol.

Authors:  Glyn Elwyn; Anne Seagrove; Kym Thorne; Wai Yee Cheung
Journal:  BMJ       Date:  2005-04-09

Review 4.  Overcoming barriers to recruitment in health research.

Authors:  Jenny Hewison; Andy Haines
Journal:  BMJ       Date:  2006-08-05

5.  Consent, confidentiality, and the Data Protection Act.

Authors:  Amy Iversen; Kathleen Liddell; Nicola Fear; Matthew Hotopf; Simon Wessely
Journal:  BMJ       Date:  2006-01-21

6.  Overcoming barriers to recruitment in health research: concerns of potential participants need to be dealt with.

Authors:  Iain K Crombie; Marion E T McMurdo; Linda Irvine; Brian Williams
Journal:  BMJ       Date:  2006-08-19

7.  National survey of British public's views on use of identifiable medical data by the National Cancer Registry.

Authors:  Geraldine Barrett; Jackie A Cassell; Janet L Peacock; Michel P Coleman
Journal:  BMJ       Date:  2006-04-28

8.  Bias from requiring explicit consent from all participants in observational research: prospective, population based study.

Authors:  Rustam Al-Shahi; Céline Vousden; Charles Warlow
Journal:  BMJ       Date:  2005-10-13

9.  Public attitudes towards the use of primary care patient record data in medical research without consent: a qualitative study.

Authors:  M R Robling; K Hood; H Houston; R Pill; J Fay; H M Evans
Journal:  J Med Ethics       Date:  2004-02       Impact factor: 2.903

10.  Selection bias resulting from the requirement for prior consent in observational research: a community cohort of people with ischaemic heart disease.

Authors:  Brian Buckley; Andrew W Murphy; Molly Byrne; Liam Glynn
Journal:  Heart       Date:  2007-05-13       Impact factor: 5.994
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  18 in total

Review 1.  Eligibility criteria in knee osteoarthritis clinical trials: systematic review.

Authors:  Yun Hyung Koog; Hyungsun Wi; Won Young Jung
Journal:  Clin Rheumatol       Date:  2013-07-23       Impact factor: 2.980

2.  Ethical and practical challenges to studying patients who opt out of large-scale biorepository research.

Authors:  S Trent Rosenbloom; Jennifer L Madison; Kyle B Brothers; Erica A Bowton; Ellen Wright Clayton; Bradley A Malin; Dan M Roden; Jill Pulley
Journal:  J Am Med Inform Assoc       Date:  2013-07-25       Impact factor: 4.497

Review 3.  Pragmatic Clinical Trials in Osteoporosis.

Authors:  Giovanni Adami; Kenneth G Saag; Maria I Danila
Journal:  Curr Osteoporos Rep       Date:  2019-12       Impact factor: 5.096

4.  Screening and detection of delirium in older ED patients: performance of the modified Confusion Assessment Method for the Emergency Department (mCAM-ED). A two-step tool.

Authors:  Wolfgang Hasemann; Florian F Grossmann; Rahel Stadler; Roland Bingisser; Dieter Breil; Martina Hafner; Reto W Kressig; Christian H Nickel
Journal:  Intern Emerg Med       Date:  2017-12-30       Impact factor: 3.397

5.  The effect of informed consent on results of a standard upper extremity intake questionnaire.

Authors:  Taylor Buckley; David Mitten; John Elfar
Journal:  J Hand Surg Am       Date:  2013-01-03       Impact factor: 2.230

6.  Vasectomy and the risk of prostate cancer: a meta-analysis of cohort studies.

Authors:  Xiao-Long Zhang; Jia-Jun Yan; Shou-Hua Pan; Jian-Gang Pan; Xiang-Rong Ying; Guan-Fu Zhang
Journal:  Int J Clin Exp Med       Date:  2015-10-15

7.  Stroke genetic research and adults with impaired decision-making capacity: a survey of IRB and investigator practices.

Authors:  Donna T Chen; James F Meschia; Thomas G Brott; Robert D Brown; Bradford B Worrall
Journal:  Stroke       Date:  2008-07-24       Impact factor: 7.914

8.  Opt-out as an acceptable method of obtaining consent in medical research: a short report.

Authors:  Akke Vellinga; Martin Cormican; Belinda Hanahoe; Kathleen Bennett; Andrew W Murphy
Journal:  BMC Med Res Methodol       Date:  2011-04-06       Impact factor: 4.615

Review 9.  Written informed consent and selection bias in observational studies using medical records: systematic review.

Authors:  Michelle E Kho; Mark Duffett; Donald J Willison; Deborah J Cook; Melissa C Brouwers
Journal:  BMJ       Date:  2009-03-12

10.  Participant recruitment in sensitive surveys: a comparative trial of 'opt in' versus 'opt out' approaches.

Authors:  Katherine J Hunt; Natalie Shlomo; Julia Addington-Hall
Journal:  BMC Med Res Methodol       Date:  2013-01-11       Impact factor: 4.615
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