Literature DB >> 19403495

More information, less understanding: a randomized study on consent issues in neonatal research.

Yvonne Freer1, Neil McIntosh, Saskia Teunisse, Kanwaljeet J S Anand, Elaine M Boyle.   

Abstract

BACKGROUND: Valid consent for research requires comprehensive and understandable information to be disclosed to participants. The way that information is shared varies, but regulatory bodies usually determine style. Some reports have suggested that although information may be all-inclusive, it does little to support understanding.
OBJECTIVE: To explore the impact of various information-sharing approaches on parents' understanding of a research study and the validity of their consent.
METHODS: This was a randomized, controlled trial. Parents of immature but well infants admitted to a large tertiary NICU in Edinburgh, Scotland, were randomly assigned within 72 hours of their infant's admission to receive 1 of 2 information leaflets, with or without a standardized verbal explanation, for a hypothetical intensive care research study. The leaflets differed in length and in the amount of detail in which the study process, risks, benefits, and patient rights were described. A questionnaire was used to elicit understanding about the purpose of the research, design of the study, procedures involved, and the consent process.
RESULTS: Forty-one parents participated in the study. Those who received the longer leaflet without verbal explanation gained only limited understanding of the purpose of the research. The procedures involved in the study were understood better by those who received the shorter leaflet. Issues relating to consent and study design were readily understood in all groups. Irrespective of documentation style, verbal explanation significantly improved understanding. Differences in understanding had little effect on whether a parent would enroll his or her infant into the study.
CONCLUSIONS: Verbal explanation significantly enhances understanding of the research process for participants regardless of the style of written documentation. However, shorter written information may lead to better understanding than lengthy, more complex documentation.

Entities:  

Mesh:

Year:  2009        PMID: 19403495     DOI: 10.1542/peds.2007-3860

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  14 in total

1.  Communication about children's clinical trials as observed and experienced: qualitative study of parents and practitioners.

Authors:  Valerie Shilling; Paula R Williamson; Helen Hickey; Emma Sowden; Michael W Beresford; Rosalind L Smyth; Bridget Young
Journal:  PLoS One       Date:  2011-07-12       Impact factor: 3.240

Review 2.  Strategies to improve recruitment to randomised trials.

Authors:  Shaun Treweek; Marie Pitkethly; Jonathan Cook; Cynthia Fraser; Elizabeth Mitchell; Frank Sullivan; Catherine Jackson; Tyna K Taskila; Heidi Gardner
Journal:  Cochrane Database Syst Rev       Date:  2018-02-22

3.  Informed consent in paediatric critical care research--a South African perspective.

Authors:  Brenda M Morrow; Andrew C Argent; Sharon Kling
Journal:  BMC Med Ethics       Date:  2015-09-09       Impact factor: 2.652

4.  Permission form synopses to improve parents' understanding of research: a randomized trial.

Authors:  C T D'Angio; H Wang; J E Hunn; G S Pryhuber; P R Chess; S Lakshminrusimha
Journal:  J Perinatol       Date:  2017-03-30       Impact factor: 2.521

5.  Investigating modifications to participant information materials to improve recruitment into a large randomized trial.

Authors:  Richard Haynes; Fang Chen; Elizabeth Wincott; Rejive Dayanandan; Michael J Lay; Sarah Parish; Louise Bowman; Martin J Landray; Jane Armitage
Journal:  Trials       Date:  2019-12-05       Impact factor: 2.279

6.  Methods to improve recruitment to randomised controlled trials: Cochrane systematic review and meta-analysis.

Authors:  Shaun Treweek; Pauline Lockhart; Marie Pitkethly; Jonathan A Cook; Monica Kjeldstrøm; Marit Johansen; Taina K Taskila; Frank M Sullivan; Sue Wilson; Catherine Jackson; Ritu Jones; Elizabeth D Mitchell
Journal:  BMJ Open       Date:  2013-02-07       Impact factor: 2.692

Review 7.  Improving understanding in the research informed consent process: a systematic review of 54 interventions tested in randomized control trials.

Authors:  Adam Nishimura; Jantey Carey; Patricia J Erwin; Jon C Tilburt; M Hassan Murad; Jennifer B McCormick
Journal:  BMC Med Ethics       Date:  2013-07-23       Impact factor: 2.652

8.  Mothers' perceptions of their child's enrollment in a randomized clinical trial: poor understanding, vulnerability and contradictory feelings.

Authors:  Adriana Assis Carvalho; Luciane Rezende Costa
Journal:  BMC Med Ethics       Date:  2013-12-10       Impact factor: 2.652

9.  Dynamic consent: a patient interface for twenty-first century research networks.

Authors:  Jane Kaye; Edgar A Whitley; David Lund; Michael Morrison; Harriet Teare; Karen Melham
Journal:  Eur J Hum Genet       Date:  2014-05-07       Impact factor: 4.246

10.  'We knew it was a totally at random thing': parents' experiences of being part of a neonatal trial.

Authors:  Merryl Harvey; Phumza Nongena; David Edwards; Maggie Redshaw
Journal:  Trials       Date:  2017-08-01       Impact factor: 2.279

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