Women and Health Research

Ethical and Legal Issues of Including Women in Clinical Studies: Volume 2: Workshop and Commissioned Papers

AvInstitute of Medicine,Division of Health Sciences Policy

Häftad, Engelska, 1994

1 449 kr

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Beskrivning

There is a growing perception that biomedical research has focused more on the health problems of men relative to those of women and that women have been denied access to advances in medical diagnosis and therapy as a result of being excluded from clinical studies. Women and Health Research, Volume 2, addresses issues connected with women's participation in clinical studies: ethical issues related to recruitment, retention, and the inclusion of pregnant women and other women of childbearing age; legal issues such as liability, compensation for injury, constitutional concerns, and federal regulations; and health consequences associated with exclusion or underrepresentation. The commissioned papers focus on the research participation of women from specific racial and ethnic groups and on whether women have been underrepresented in biomedical research, based on a systematic survey of clinical studies reported in a prominent medical journal.

Produktinformation

Utgivningsdatum:1994-01-01
Mått:152 x 229 x 25 mm
Vikt:426 g
Format:Häftad
Språk:Engelska
Antal sidor:261
Förlag:National Academies Press
ISBN:9780309050401

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Mer om författaren

Anna C. Mastroianni, Ruth Faden, and Daniel Federman, Editors; Committee on the Ethical and Legal Issues Relating to the Inclusion of Women in Clinical Studies, Institute of Medicine

Innehållsförteckning

1 Front Matter; 2 1 Women's Participation in Clinical Research: From Protectionism to Access; 3 2 Women in Clinical Studies: A Feminist View; 4 3 Ethical Issues Related to the Inclusion of Pregnant Women in Clinical Trials (I); 5 4 Ethical Issues Related to the Inclusion of Pregnant Women in Clinical Trial (II); 6 5 Ethical Issues Related to the Inclusion of Women of Childbearing Age in Clinical Trials; 7 6 Health Consequences of Exclusion or Underrepresentation of Women in Clinical Studies (I); 8 7 Health Consequences of Exclusion or Underrepresentation of Women in Clinical Studies (II); 9 8 Recruitment and Retention of Women in Clinical Studies: Theoretical Perspectives and Methodological Considerations; 10 9 Recruitment and Retention of Women of Color in Clinical Studies; 11 10 Recruitment and Retention of Women in Clinical Studies: Ethical Considerations; 12 11 Impact of Current Federal Regulations on the Inclusion of Female Subjects in Clinical Studies; 13 12 Brief Overvew of Constitutional Issues Raised by the Exclusion of Women from Research Trials; 14 13 Liability Exposure for Exclusion and Inclusion of Women as Subjects in Clinical Studies; 15 14 Liability Exposure When Offspring Are Injured Because of Their Parents' Participation in Clinical Trials; 16 15 Compensation for Research Injuries; 17 16 Justice and the Inclusion of Women in Clinical Studies: A Conceptual Framework; 18 17 Women's Representation as Subjects in Clinical Studies: A Pilot Study of Research Published in JAMA in 1990 and 1992; 19 18 Racial Differentials in Medical Care: Implications for Research on Women; 20 19 Health Status of American Indian and Alaska Native Women; 21 20 Ethical and Legal Issues Relating to the Inclusion of Asian/Pacific Islanders in Clinical Studies; 22 21 The Inclusion of Latino Women in Clinical and Research Studies: Scientific Suggestions for Assuring Legal and Ethical Integrity; 23 Appendix: Author Biographies

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