Literature DB >> 16319237

Children's understanding of the risks and benefits associated with research.

T M Burke1, R Abramovitch, S Zlotkin.   

Abstract

OBJECTIVE: The objective of the current study was to maximise the amount of information children and adolescents understand about the risks and benefits associated with participation in a biomedical research study.
DESIGN: Participants were presented with one of six hypothetical research protocols describing how to fix a fractured thigh using either a "standard" cast or "new" pins procedure. Risks and benefits associated with each of the treatment options were manipulated so that for each one of the six protocols there was either a correct or ambiguous choice. PARTICIPANTS AND
SETTING: Two hundred and fifty one children, ages 6-15 (53% boys), and 237 adults (30% men) were interviewed while waiting for a clinic appointment at the Hospital for Sick Children.
RESULTS: Using standardised procedures and questionnaires, it was determined that most participants, regardless of age group, were able to understand the basic purpose and procedures involved in the research, and most were able to choose the "correct" operation. The younger children, however, showed an overall preference for a cast operation, whereas the older participants were more likely to choose the pins.
CONCLUSIONS: By creating age appropriate modules of information, children as young as six years can understand potentially difficult and complex concepts such as the risks and benefits associated with participation in biomedical research. It appears, however, that different criteria were used for treatment preference, regardless of associated risks; older participants tended to opt for mobility (the pins procedure) whereas younger participants stayed with the more familiar cast operation.

Entities:  

Keywords:  Biomedical and Behavioral Research; Empirical Approach

Mesh:

Year:  2005        PMID: 16319237      PMCID: PMC1734064          DOI: 10.1136/jme.2003.003228

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


  14 in total

1.  Are research participants truly informed? Readability of informed consent forms used in research.

Authors:  James R P Ogloff; Randy K Otto
Journal:  Ethics Behav       Date:  1991

2.  Enhancing comprehension of information for informed consent: a review of empirical research.

Authors:  Mary Cipriano Silva; Jeanne Merkle Sorrell
Journal:  IRB       Date:  1988 Jan-Feb

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4.  Informed consent -- why are its goals imperfectly realized?

Authors:  B R Cassileth; R V Zupkis; K Sutton-Smith; V March
Journal:  N Engl J Med       Date:  1980-04-17       Impact factor: 91.245

5.  The competency of children and adolescents to make informed treatment decisions.

Authors:  L A Weithorn; S B Campbell
Journal:  Child Dev       Date:  1982-12

6.  Children's capacity to agree to psychological research: knowledge of risks and benefits and voluntariness.

Authors:  Rona Abramovitch; Jonathan L Freedman; Kate Henry; Michelle Van Brunschot
Journal:  Ethics Behav       Date:  1995

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8.  Participation in biomedical research: the consent process as viewed by children, adolescents, young adults, and physicians.

Authors:  E J Susman; L D Dorn; J C Fletcher
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9.  Empirical examination of the ability of children to consent to clinical research.

Authors:  N Ondrusek; R Abramovitch; P Pencharz; G Koren
Journal:  J Med Ethics       Date:  1998-06       Impact factor: 2.903

10.  Putting the 'informed' into 'consent': a matter of plain language.

Authors:  J B Green; R E Duncan; G L Barnes; F Oberklaid
Journal:  J Paediatr Child Health       Date:  2003-12       Impact factor: 1.954

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  13 in total

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Journal:  J Pediatr Pharmacol Ther       Date:  2012-07

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Authors:  David G Scherer; Janet L Brody; Robert D Annett; Charles Turner; Jeanne Dalen; Yesel Yoon
Journal:  AJOB Prim Res       Date:  2013

Review 6.  Understanding Ethical Issues of Research Participation From the Perspective of Participating Children and Adolescents: A Systematic Review.

Authors:  Stacey Crane; Marion E Broome
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7.  Overcoming burdens in the regulation of clinical research in children. Proceedings of a consensus conference, in historical context.

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8.  Child's assent in research: age threshold or personalisation?

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Journal:  BMC Med Ethics       Date:  2014-06-13       Impact factor: 2.652

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10.  Ethics takes time, but not that long.

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