Literature DB >> 19717698

Performance-based readability testing of participant materials for a phase I trial: TGN1412.

P Knapp1, D K Raynor, J Silcock, B Parkinson.   

Abstract

BACKGROUND: Concern has been expressed about the process of consent to clinical trials, particularly in phase I "first-in-man" trials. Trial participant information sheets are often lengthy and technical. Content-based readability testing of sheets, which is often required to obtain research ethics approval for trials in the USA, is limited and cannot indicate how information will perform.
METHODS: An independent-groups design was used to study the user-testing performance of the participant information sheet from the phase I TGN1412 trial. Members of the public were asked to read it, then find and demonstrate understanding of 21 key aspects of the trial. The participant information sheet was then rewritten, redesigned and tested on 20 members of the public, using the same 21-item questionnaire.
RESULTS: On the original TGN1412 participant information sheet, participants could not find answers and some of the found information was not understood. Six of 21 questions, including those relating to placebo, follow-up visits and the emergency phone number, were found by eight or fewer of 10 participants. The revised information sheet performed better, with the answers to 17 of 21 questions found and understood by all 20 participants.
CONCLUSIONS: Tests showed that the TGN1412 participant information sheet may not inform participants adequately for consent. Revising its content and design led to significant improvements. Writers of materials for trial participants should take account of good practice in information design. Performance-based user testing may be a useful method to indicate strengths and weaknesses in trial materials.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19717698     DOI: 10.1136/jme.2008.026708

Source DB:  PubMed          Journal:  J Med Ethics        ISSN: 0306-6800            Impact factor:   2.903


  18 in total

1.  Achieving new levels of recall in consent to research by combining remedial and motivational techniques.

Authors:  David S Festinger; Karen L Dugosh; Douglas B Marlowe; Nicolle T Clements
Journal:  J Med Ethics       Date:  2013-04-04       Impact factor: 2.903

2.  Can user testing of a clinical trial patient information sheet make it fit-for-purpose?--a randomized controlled trial.

Authors:  Peter Knapp; David K Raynor; Jonathan Silcock; Brian Parkinson
Journal:  BMC Med       Date:  2011-07-21       Impact factor: 8.775

3.  Improving recruitment to a study of telehealth management for long-term conditions in primary care: two embedded, randomised controlled trials of optimised patient information materials.

Authors:  Mei-See Man; Jo Rick; Peter Bower
Journal:  Trials       Date:  2015-07-19       Impact factor: 2.279

4.  Systematic techniques for assisting recruitment to trials (START): study protocol for embedded, randomized controlled trials.

Authors:  Jo Rick; Jonathan Graffy; Peter Knapp; Nicola Small; David J Collier; Sandra Eldridge; Anne Kennedy; Chris Salisbury; Shaun Treweek; David Torgerson; Paul Wallace; Vichithranie Madurasinghe; Adwoa Hughes-Morley; Peter Bower
Journal:  Trials       Date:  2014-10-25       Impact factor: 2.279

5.  The design and user-testing of a question prompt list for attention-deficit/hyperactivity disorder.

Authors:  Rana Ahmed; David K Raynor; Kirsten J McCaffery; Parisa Aslani
Journal:  BMJ Open       Date:  2014-12-16       Impact factor: 2.692

6.  Improved participants' understanding in a healthy volunteer study using the SIDCER informed consent form: a randomized-controlled study.

Authors:  Nut Koonrungsesomboon; Supanimit Teekachunhatean; Nutthiya Hanprasertpong; Junjira Laothavorn; Kesara Na-Bangchang; Juntra Karbwang
Journal:  Eur J Clin Pharmacol       Date:  2015-12-29       Impact factor: 2.953

7.  Developing and evaluating multimedia information resources to improve engagement of children, adolescents, and their parents with trials (TRECA study): Study protocol for a series of linked randomised controlled trials.

Authors:  Jacqueline Martin-Kerry; Peter Bower; Bridget Young; Jonathan Graffy; Rebecca Sheridan; Ian Watt; Paul Baines; Catherine Stones; Jennifer Preston; Steven Higgins; Carrol Gamble; Peter Knapp
Journal:  Trials       Date:  2017-06-08       Impact factor: 2.279

8.  Performance-based readability testing of participant information for a Phase 3 IVF trial.

Authors:  Peter Knapp; D K Raynor; Jonathan Silcock; Brian Parkinson
Journal:  Trials       Date:  2009-09-01       Impact factor: 2.279

9.  The impact of advertising patient and public involvement on trial recruitment: embedded cluster randomised recruitment trial.

Authors:  Adwoa Hughes-Morley; Mark Hann; Claire Fraser; Oonagh Meade; Karina Lovell; Bridget Young; Chris Roberts; Lindsey Cree; Donna More; Neil O'Leary; Patrick Callaghan; Waquas Waheed; Peter Bower
Journal:  Trials       Date:  2016-12-08       Impact factor: 2.279

10.  Participatory improvement of a template for informed consent documents in biobank research - study results and methodological reflections.

Authors:  Sabine Bossert; Hannes Kahrass; Ulrike Heinemeyer; Jana Prokein; Daniel Strech
Journal:  BMC Med Ethics       Date:  2017-12-20       Impact factor: 2.652

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.