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Human subjects protection: An event monitoring committee for research studies of girls from breast cancer families

  • Diana Harris
  • , Linda Patrick-Miller
  • , Lisa Schwartz
  • , John Lantos
  • , Chris Daugherty
  • , Mary Daly
  • , Irene L. Andrulis
  • , Saundra S. Buys
  • , Wendy K. Chung
  • , Caren J. Frost
  • , Esther M. John
  • , Theresa H.M. Keegan
  • , Julia A. Knight
  • , Mary Beth Terry
  • , Angela R. Bradbury
  • University of Pennsylvania
  • University of Chicago
  • The Children's Hospital of Philadelphia
  • University of Missouri at Kansas City
  • Fred A. Litwin Center for Cancer Genetics
  • University of Utah
  • Columbia University
  • Cancer Prevention Institute of California
  • Stanford University
  • University of Toronto

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Purpose Researchers must monitor the safety of research participants, particularly in studies involving children and adolescents. Yet, there is limited guidance for the development and implementation of oversight committees for psychosocial, behavioral intervention, and observational studies. Methods We implemented a model for an Event Monitoring Committee (EMC) in three related studies recruiting 6- to 19-year-old girls from families with and without breast cancer. Results The EMC model can be valuable for investigators and local institutional review boards when additional oversight is desired. Recommendations are provided and intended to be broadly applicable to a wide range of research activities designed to improve the health of children, adolescents, and families. EMC goals, membership, and procedures for monitoring and assessing risks and benefits should be defined but should also be flexible and tailored to the study design and population. The EMC model also provides an independent comprehensive, study-wide oversight mechanism for multicenter psychosocial, behavioral intervention, and observational studies. Conclusions An EMC provides an alternative oversight approach where additional independent assessment and oversight of study-related risks are desired, particularly in the setting of vulnerable populations, children and adolescents, or where risks nontraditional to the medical field (i.e., social, emotional, or cultural) are possible.

Original languageEnglish
Pages (from-to)352-357
Number of pages6
JournalJournal of Adolescent Health
Volume55
Issue number3
DOIs
StatePublished - Sep 2014

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Adolescent
  • Biomedical Research/ethics
  • Breast Neoplasms
  • Child
  • Ethics Committees, Research
  • Female
  • Humans
  • Informed Consent/ethics
  • Patient Selection/ethics
  • Research Design
  • Research Subjects
  • United States
  • Vulnerable Populations
  • Young Adult

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