Literature DB >> 17403829

Improving informed consent: suggestions from parents of children with leukemia.

Michelle L Eder1, Amy D Yamokoski, Peter W Wittmann, Eric D Kodish.   

Abstract

OBJECTIVE: The objective of this study was to report suggestions for improving the informed consent process from the perspective of parents of children with leukemia.
METHODS: Recommendations for improving informed consent were elicited from 140 parents of children who had been offered participation in a randomized clinical trial for the treatment of their acute leukemia. Four different methods and data collection time points were used with this group of parents, including open-ended, in-person interviews within 72 hours after the informed consent conference; follow-up telephone interviews 6 months after diagnosis; focus groups during year 3 of the project; and a parent advisory group on informed consent meeting in year 4.
RESULTS: The most frequently cited suggestions for improving informed consent during the interviews and focus groups related to giving parents more time to make their decision, the amount and type of information provided, organization of the consent conference, communication style, and providing additional materials. During the parent advisory group on informed consent meeting, parents developed specific guidelines for organization of the information that is presented during the consent process that include 7 major components: timing, sequence, checklist, checking for understanding, anticipatory guidance, segue into randomized clinical trial discussion with historical perspective, and choice.
CONCLUSIONS: Through the incorporation of parental perspectives that provide an authentic stakeholder voice, our research represents a true partnership approach to improving the consent process. Parents provided practical advice for improving informed consent that can be applied to most adult and pediatric patient populations.

Entities:  

Mesh:

Year:  2007        PMID: 17403829     DOI: 10.1542/peds.2006-2208

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


  35 in total

1.  Attitudes of Mothers Regarding Willingness to Enroll Their Children in Research.

Authors:  Jane Paik Kim; Maryam Rostami; Laura Weiss Roberts
Journal:  J Empir Res Hum Res Ethics       Date:  2020-06-18       Impact factor: 1.742

2.  Practical communication guidance to improve phase 1 informed consent conversations and decision-making in pediatric oncology.

Authors:  Liza-Marie Johnson; Angela C Leek; Dennis Drotar; Robert B Noll; Susan R Rheingold; Eric D Kodish; Justin N Baker
Journal:  Cancer       Date:  2015-04-14       Impact factor: 6.860

3.  Parent participation and physician-parent communication during informed consent in child leukemia.

Authors:  Melissa Cousino; Rebecca Hazen; Amy Yamokoski; Victoria Miller; Stephen Zyzanski; Dennis Drotar; Eric Kodish
Journal:  Pediatrics       Date:  2011-11-07       Impact factor: 7.124

4.  Satisfaction with the decision to participate in cancer clinical trials is high, but understanding is a problem.

Authors:  M Jefford; L Mileshkin; J Matthews; H Raunow; C O'Kane; T Cavicchiolo; H Brasier; M Anderson; J Reynolds
Journal:  Support Care Cancer       Date:  2010-02-23       Impact factor: 3.603

5.  SUPPORTing premature infants.

Authors:  John D Lantos
Journal:  Pediatrics       Date:  2013-11-11       Impact factor: 7.124

6.  Stem cell clinical trials for spinal cord injury: readiness, reluctance, redefinition.

Authors:  J Illes; J C Reimer; B K Kwon
Journal:  Stem Cell Rev Rep       Date:  2011-11       Impact factor: 5.739

7.  Processing Information After a Child's Cancer Diagnosis-How Parents Learn.

Authors:  Cheryl C Rodgers; Kristin Stegenga; Janice S Withycombe; Karen Sachse; Katherine Patterson Kelly
Journal:  J Pediatr Oncol Nurs       Date:  2016 Nov/Dec       Impact factor: 1.636

Review 8.  Clinical trials in children.

Authors:  Pathma D Joseph; Jonathan C Craig; Patrina H Y Caldwell
Journal:  Br J Clin Pharmacol       Date:  2015-03       Impact factor: 4.335

9.  Improving informed consent with minority participants: results from researcher and community surveys.

Authors:  Sandra Crouse Quinn; Mary A Garza; James Butler; Craig S Fryer; Erica T Casper; Stephen B Thomas; David Barnard; Kevin H Kim
Journal:  J Empir Res Hum Res Ethics       Date:  2012-12       Impact factor: 1.742

10.  Balancing high accrual and ethical recruitment in paediatric oncology: a qualitative study of the 'look and feel' of clinical trial discussions.

Authors:  Lucie M T Byrne-Davis; Peter Salmon; Katja Gravenhorst; Tim O B Eden; Bridget Young
Journal:  BMC Med Res Methodol       Date:  2010-10-22       Impact factor: 4.615

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