Journal of Adolescent Health
Volume 41, Issue 1 , Pages 14-18 , July 2007

STI Research: Recruiting an Unbiased Sample

  • Jennifer L. Reed, M.D.

      Affiliations

    • Division of Emergency Medicine, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio
    • Corresponding Author InformationAddress correspondence to: Dr. Jennifer L. Reed, Division of Emergency Medicine, Cincinnati Children’s Hospital Medical Center, 3333 Burnet Avenue ML 2008, Cincinnati, Ohio 45229.
  • ,
  • Julie M. Thistlethwaite, B.S.

      Affiliations

    • University of Cincinnati College of Medicine, Cincinnati, Ohio
  • ,
  • Jill S. Huppert, M.D., M.P.H.

      Affiliations

    • Division of Adolescent Medicine, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio

Received 1 September 2006 ,Accepted 9 February 2007.

References 

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  2. English A, Kenney K. State Minor Consent Laws: A Summary. 2nd edn.. Chapel Hill, NC: Center for Adolescent Health & the Law; 2003;
  3. Reddy DM, Fleming R, Swain C. Effect of mandatory parental notification on adolescent girls’ use of sexual health care services. JAMA. 2002;288(6):710–714
  4. Stanford PD, Monte DA, Briggs FM, et al. Recruitment and retention of adolescent participants in HIV research: findings from the REACH (Reaching for Excellence in Adolescent Care and Health) Project. J Adolesc Health. 2003;32(3):192–203
  5. Geluda K, Bisaglia JB, Moreira V, et al. Third-party informed consent in research with adolescents: the good, the bad and the ugly. Soc Sci Med. 2005;61(5):985–988
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  7. Mammel KA, Kaplan DW. Research consent by adolescent minors and institutional review boards. J Adolesc Health. 1995;17(5):323–330
  8. American College of Obstetricians and Gynecologists Committee on Adolescent Health Care. ACOG Committee Opinion #302: Guidelines for Adolescent Health Research. Obstet Gynecol. 2004;104(4):899–901Oct
  9. Santelli JS, Smith Rogers A, Rosenfeld WD, et al. Guidelines for adolescent health research: a position paper of the Society for Adolescent Medicine. J Adolesc Health. 2003;33:396–409
  10. National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research. The Belmont Report: Ethical Principles and Guidelines for the Protection of Human Subjects of Research. Washington, DC: U.S. Department of Health and Human Services; 1979;
  11. National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research. Report and Recommendations: Research Involving Children (Recommendation 8). Washington, DC: US Department of Health Education and Welfare; 1977;[Report No.: DHEW Pub. No. (05)77-0004]
  12. Protection of Human Subjects. 2005;Code of Federal Regulations, Title 45 (Rev), Part 46.116 (d)
  13. Protection of Human Subjects. 2005;Code of Federal Regulations, Title 45 (Rev), Part 46.408(c)
  14. Kimberly MB, Hoehn KS, Feudtner C, et al. Variation in standards of research compensation and child assent practices: a comparison of 69 institutional review board-approved informed permission and assent forms for 3 multicenter pediatric clinical trials. Pediatrics. 2006;117(5):1706–1711
  15. Whittle A, Shah S, Wilfond B, et al. Institutional review board practices regarding assent in pediatric research. Pediatrics. 2004;113(6):1747–1752
  16. Freimuth VS, Quinn SC, Thomas SB, et al. African Americans’ views on research and the Tuskegee Syphilis Study. Soc Sci Med. 2001;52(5):797–808
  17. Woolf SH, Rothemich SF, Johnson RE, et al. Selection bias from requiring patients to give consent to examine data for health services research. Arch Fam Med. 2000;9(10):1111–1118
  18. Nathanson C, Becker M. Family and peer influence on obtaining a method of contraception. J Marriage Fam. 1986;43(3):513–525
  19. Tanfer K, Cubbins LA, Billy JO. Gender, race, class and self-reported sexually transmitted disease incidence. Fam Plann Perspect. 1995;27(5):196–202

PII: S1054-139X(07)00103-6

doi: 10.1016/j.jadohealth.2007.02.010

Journal of Adolescent Health
Volume 41, Issue 1 , Pages 14-18 , July 2007