The research will explore the ethical and policy issues raised by the participation of children in medical research. The goals of this project are: 1) to show that the current safeguards are inadequate and that there are systemic breeches of research ethics standards; and 2) to motivate policy makers, health care analysts, and the leaders of medicine to change practice and policy regarding the participation of children in research Specifically, the broad objectives of the project are: 1) to examine the ethical issues raised by the participation of children in research, and the need to balance access and protection; 2) to assess the ethical and policy implications of the new national policies and commissioned reports regarding the participation of children in research; 3) to identify recent published pediatric research that supports the thesis that current policies and practices are inadequate protection of children-subjects; and 4) to make policy recommendations to re-equilibrate the balance between protection and access. The main outcome of the research will be a book that offers a sustained ethical and policy critique of current policies, guidelines, and statements. The book will be entitled: Children in Medical Research: An Ethical and Policy Challenge. The book is divided into five sections. Part I addresses the problem and the current solutions and includes a historical overview of the regulations of children in research and an analytical critique of current policies, regulations and guidelines. Part H is entitled Beecher Revisited and addresses current research controversies including a chapter on placebo-controlled clinical trials, research involving healthy children and """"""""at risk"""""""" children, genetic research, and phase I cancer research. Part Ill addresses barriers to pediatric research and includes chapters on funding, recruitment, incentives, retention of subjects, and informed consent issues. Part IV addresses research on special populations including newborns and adolescents. Part V offers revised policy recommendations.

Agency
National Institute of Health (NIH)
Institute
National Library of Medicine (NLM)
Type
Health Sciences Publication Support Awards (NLM) (G13)
Project #
5G13LM007472-02
Application #
6528427
Study Section
Special Emphasis Panel (ZLM1-MMR-P (O1))
Program Officer
Florance, Valerie
Project Start
2001-09-30
Project End
2004-09-29
Budget Start
2002-09-30
Budget End
2003-09-29
Support Year
2
Fiscal Year
2002
Total Cost
$75,500
Indirect Cost
Name
University of Chicago
Department
Pediatrics
Type
Schools of Medicine
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Ross, Lainie Friedman (2011) In defense of the American Academy of Pediatrics policy statement--children as hematopoietic stem cell donors. Pediatr Blood Cancer 56:520-3
Kelly, Michael L; Ackerman, Paul D; Ross, Lainie Friedman (2005) The participation of minorities in published pediatric research. J Natl Med Assoc 97:777-83
Ross, Lainie Friedman (2005) Lessons to be learned from the 407 process. Health Matrix Clevel 15:401-21
Ross, Lainie Friedman (2004) Informed consent in pediatric research. Camb Q Healthc Ethics 13:346-58
Coffey, M Justin; Wilfond, Benjamin; Ross, Lainie Friedman (2004) Ethical assessment of clinical asthma trials including children subjects. Pediatrics 113:87-94
Ross, Lainie Friedman (2004) Children in medical research: balancing protection and access--has the pendulum swung too far? Perspect Biol Med 47:519-36
Cooper, Zachary N; Nelson, Robert M; Ross, Lainie Friedman (2004) Certificates of confidentiality in research: rationale and usage. Genet Test 8:214-20
Coffey, M Justin; Ross, Lainie (2004) Human subject protections in genetic research. Genet Test 8:209-13
Ross, Lainie Friedman (2003) Responding to the challenge of the children's health act: an introduction to children in research. Theor Med Bioeth 24:101-6
Walsh, Catherine; Ross, Lainie F (2003) Are minority children under- or overrepresented in pediatric research? Pediatrics 112:890-5

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