Commentary on Special Issue on Informed Consent With Families of Ill Children (February 2001): Understanding Devastation and Difference in Informed Permission and Assent

Journal of Family Nursing

Volumn 7, Issue 2, 2001, Pages 208-213

  Nelson, Robert M ^a   Rushton, Cindy Hylton ^b  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b JOHNS HOPKINS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84990397465     PISSN: 10748407     EISSN: None     Source Type: Journal    
DOI: 10.1177/107484070100700205     Document Type: Article

References (6)

1. Broome, M. E., Richards, D. J., & Hall, J. (2001). Children in research: The experience of ill children and adolescents. Journal of Family Nursing, 7, 32-49.
2. Hall, J. M., Stevens, P. E., & Pletsch, P. K. (2001). Team research using qualitative methods: Investigating children's involvement in clinical research. Journal of Family Nursing, 7, 7-31.
3. Liaschenko, J., & Underwood, S. M. (2001). Children in research: Fathers in cancer research—Meanings and reasons for participation. Journal of Family Nursing, 7, 71-91.
4. National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research. (1979). The Belmont report: Ethical principles and guidelines for the protection of human subjects of research (RN Doc 79-12065). Washington, DC: Government Printing Office.
5. Pletsch, P. K., & Stevens, P. E. (2001). Children in research: Informed consent and critical factors affecting mothers. Journal of Family Nursing, 7, 50-70.
6. Snethen, J., & Broome, M. E. (2001). Children in research: The experiences of siblings in research as a family affair. Journal of Family Nursing, 7, 92-110.