Improving informed consent: pilot of a decision aid for women invited to participate in a breast cancer prevention trial (IBIS‐II DCIS)

Juraskova, Ilona; Butow, Phyllis; Lopez, Anna-Lena; Seccombe, M; Coates, Alan S.; Boyle, F; McCarthy, Nicole; Reaby, Linda; Forbes, JF

doi:10.1111/j.1369-7625.2008.00498.x

Cited by 55 publications

(61 citation statements)

References 35 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…This conceptualisation as a deliberate decision between healthcare options helps place the decision in the context of patients' illness management and lifestyle. Our findings add to others' evidence for trial information to be framed in the context of patients' illness management (Abhyankar et al, 2014;Brown et al, 2004;Entwistle, 2008;Gillies et al, 2014;Juraskova et al, 2008;Juraskova et al, 2014).…”

Section: Discussionmentioning

confidence: 75%

“…This could be achieved by 1) improving information in consent to help patients' active decision making between consequences of other treatment options and consequences of taking part in trial (Abhyankar et al, 2011). A decision aid (DA) developed by Juraskova et al (2008; to assist women's decision making about participation in a cancer prevention trial has shown promising results in improving understanding, reducing decisional regret and enhancing decision quality over and above the usual consent information. The DA presents an explicit choice between the trial participation and standard care options, which is a more balanced and complete presentation than the choice between 'trial' and 'no trial' (Abhyankar et al, 2013; trial is embedded appropriately in care pathway and 3) training to non-trial staff in how to provide information about the trial in the context of delivering care (Mills et al, 2014).…”

Section: Implications For Practicementioning

confidence: 99%

See 1 more Smart Citation

Identifying components in consent information needed to support informed decision making about trial participation: An interview study with women managing cancer

Abhyankar

Velikova

Summers³

et al. 2016

Social Science & Medicine

View full text Add to dashboard Cite

Authors' contributionsPA made substantial contributions to conception and design, acquisition of data, analysis and interpretation of data, drafting the manuscript and revising it critically for important intellectual content and gave final approval of the version to be published.GV made substantial contribution as a clinical supervisor to conception and design, interpretation of data, and revising the manuscript critically for important intellectual content and gave final approval of the version to be published. BS made substantial contribution as an academic supervisor to interpretation of data, and revising the manuscript critically for important intellectual content and gave final approval of the version to be published.HLB made substantial contribution as lead supervisor to conception and design, analysis and interpretation of data, drafting the manuscript and revising it critically for important intellectual content and gave final approval of the version to be published. AcknowledgementsWe would like to acknowledge the research nurses at the oncology outpatient clinic who helped in patient recruitment and all patients who took part in the study. We would also like to thank Dr Fiona Harris for advice on qualitative aspects of this paper and helpful comments from the anonymous peer reviewers, both of which have significantly improved the manuscript. 4Identifying components in consent information needed to support informed decision making about trial participation: an interview study with women managing cancer Abstract Background: Research governance requires patients give informed consent to participate in

show abstract

Section: Discussionmentioning

confidence: 75%

Section: Implications For Practicementioning

confidence: 99%

Identifying components in consent information needed to support informed decision making about trial participation: An interview study with women managing cancer

Abhyankar

Velikova

Summers³

et al. 2016

Social Science & Medicine

View full text Add to dashboard Cite

show abstract

“…Decision aids are thought to be valuable to adult patients when making difficult treatment or screening decisions. The value of these aids in helping adult patients make decisions about clinical trials has also been reported 153 and further studies are under way in adult trials. 154 The value of decision aids for parents considering a trial for their child has not yet been investigated.…”

Section: Discussing Trials With Parentsmentioning

confidence: 99%

Processes in recruitment to randomised controlled trials of medicines for children (RECRUIT): a qualitative study

Shilling

Williamson²,

Hickey³

et al. 2011

Health Technol Assess

View full text Add to dashboard Cite

How to obtain copies of this and other HTA programme reports An electronic version of this title, in Adobe Acrobat format, is available for downloading free of charge for personal use from the HTA website (www.hta.ac.uk). A fully searchable DVD is also available (see below).Printed copies of HTA journal series issues cost £20 each (post and packing free in the UK) to both public and private sector purchasers from our despatch agents.Non-UK purchasers will have to pay a small fee for post and packing. For European countries the cost is £2 per issue and for the rest of the world £3 per issue. How to order:-fax (with credit card details) -post (with credit card details or cheque) -phone during office hours (credit card only).Additionally the HTA website allows you to either print out your order or download a blank order form. Contact details are as follows:Synergie UK (HTA Department) Digital House, The Loddon Centre Wade Road Basingstoke Hants RG24 8QW Email: orders@hta.ac.uk Tel: 0845 812 4000 -ask for 'HTA Payment Services' (out-of-hours answer-phone service) Fax: 0845 812 4001 -put 'HTA Order' on the fax header Payment methods Paying by chequeIf you pay by cheque, the cheque must be in pounds sterling, made payable to University of Southampton and drawn on a bank with a UK address.Paying by credit card You can order using your credit card by phone, fax or post. SubscriptionsNHS libraries can subscribe free of charge. Public libraries can subscribe at a reduced cost of £100 for each volume (normally comprising 40-50 titles). The commercial subscription rate is £400 per volume (addresses within the UK) and £600 per volume (addresses outside the UK). Please see our website for details. Subscriptions can be purchased only for the current or forthcoming volume.How do I get a copy of HTA on DVD?Please use the form on the HTA website (www.hta.ac.uk/htacd/index.shtml). HTA on DVD is currently free of charge worldwide.The website also provides information about the HTA programme and lists the membership of the various committees. HTAProcesses in recruitment to randomised controlled trials of medicines for children (RECRUIT): a qualitative study NIHR Health Technology Assessment programmeThe Health Technology Assessment (HTA) programme, part of the National Institute for Health Research (NIHR), was set up in 1993. It produces high-quality research information on the effectiveness, costs and broader impact of health technologies for those who use, manage and provide care in the NHS. 'Health technologies' are broadly defined as all interventions used to promote health, prevent and treat disease, and improve rehabilitation and long-term care. The research findings from the HTA programme directly influence decision-making bodies such as the National Institute for Health and Clinical Excellence (NICE) and the National Screening Committee (NSC). HTA findings also help to improve the quality of clinical practice in the NHS indirectly in that they form a key component of the 'National Knowledge Service' . The HTA programme is n...

show abstract

“…However, there is less discussion of the difficulties associated with undertaking such studies, including costs 2 , ethical problems, issues associated with informed consent 3 , problems of bias, clinician preference for certain treatment options 4 , difficulties in recruiting sufficient patients 5 and overestimating the number of patients who would be eligible for inclusion in the study or would agree to participate 6 .…”

Section: Introductionmentioning

confidence: 99%

In search of the sample: Recent experiences of a trial team in Orthodontics

Cunningham

Bearn

Benson

et al. 2011

Contemporary Clinical Trials

View full text Add to dashboard Cite

Randomised clinical trials are commonly undertaken in medical and dental research.However, few authors discuss the difficulties associated with such studies, including costs, ethical issues and recruitment of an adequate number of patients. There is little information available on the number of studies which are terminated early as a result of these issues, but it seems likely that at least 10% of clinical studies never reach completion. This paper reviews two nationally funded clinical studies which were terminated early and highlights the recruitment issues which were encountered in order to bring certain issues to the attention of other researchers.3

show abstract

Improving informed consent: pilot of a decision aid for women invited to participate in a breast cancer prevention trial (IBIS‐II DCIS)

Abstract: Background Patients and clinicians report difficulties with the process of informed consent to clinical trials and audiotape audits show that critical information is often omitted or poorly presented. Decision aids (DAs) may assist in improving consent.

Cited by 55 publications

References 35 publications

Identifying components in consent information needed to support informed decision making about trial participation: An interview study with women managing cancer

Identifying components in consent information needed to support informed decision making about trial participation: An interview study with women managing cancer

Processes in recruitment to randomised controlled trials of medicines for children (RECRUIT): a qualitative study

In search of the sample: Recent experiences of a trial team in Orthodontics

Contact Info

Product

Resources

About