Reaching the hard-to-reach: a systematic review of strategies for improving health and medical research with socially disadvantaged groups

Author:

Bonevski Billie,Randell Madeleine,Paul Chris,Chapman Kathy,Twyman Laura,Bryant Jamie,Brozek Irena,Hughes Clare

Publisher

Springer Science and Business Media LLC

Subject

Health Informatics,Epidemiology

Reference167 articles.

1. National Institute of Health (NIH): Guidelines on the inclusion of women and minorities as subjects in clinical research. NIH Guide. 1994, 23: 2-3.

2. Heiat A, Gross CP, Krumholz HM: Representation of the Elderly, Women, and Minorities in Heart Failure Clinical Trials. Arch Intern Med. 2002, 162 (15): doi:10.1001/archinte.162.15.1682

3. Johnson MS: Generalizability of clinical trials using homogenous samples – a metaanalysis. J Assoc Acad Minor Phys. 1990, 1: 31-33.

4. Rogers WA: Evidence based medicine and justice: a framework for looking at the impact of EBM upon vulnerable or disadvantaged groups. J Med Ethics. 2004, 30: 141-145. 10.1136/jme.2003.007062. doi: 10.1136/jme.2003.007062

5. Albain KS, Unger JM, Crowley JJ, Coltman CA, Hershman DL: Racial disparities in cancer survival among randomised clinical trial patients of the Southwest Oncology Group. J Natl Cancer Inst. 2009, 101: 984-992. 10.1093/jnci/djp175.

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