Literature DB >> 10363220

Informed consent in school health research: why, how, and making it easy.

J G Ross1, E C Sundberg, K H Flint.   

Abstract

The obligation to obtain informed consent for student participation in health-related research creates a complex set of legal, ethical, and administrative responsibilities because the interests of research integrity are delicately balanced against protection of human subjects. Even the term itself sparks a range of responses depending on one's perspective and stake in the process. This paper traces the historical impetus behind obtaining informed consent, identifies key elements comprising informed consent, and reviews types of consent procedures used in schools. The authors suggest 20 ways to boost response rates while providing a realistic level of informed consent for school-based studies.

Entities:  

Keywords:  Biomedical and Behavioral Research

Mesh：

Year:  1999        PMID： 10363220     DOI： 10.1111/j.1746-1561.1999.tb06378.x

Source DB:  PubMed          Journal:  J Sch Health        ISSN： 0022-4391            Impact factor:   2.118


  8 in total

1.  Recruiting a diverse group of middle school girls into the trial of activity for adolescent girls.

Authors:  John P Elder; Laverne Shuler; Stacey G Moe; Mira Grieser; Charlotte Pratt; Sandra Cameron; Melanie Hingle; Julie L Pickrel; Brit I Saksvig; Kenneth Schachter; Susan Greer; Elizabeth K Guth Bothwell
Journal:  J Sch Health       Date:  2008-10       Impact factor: 2.118

2.  Comparison of enrollment rates of African-American families into a school-based tobacco prevention trial using two recruitment strategies in urban and rural settings.

Authors:  Martha S Tingen; Jeannette O Andrews; Janie Heath; Ashley E Turnmire; Jennifer L Waller; Frank A Treiber
Journal:  Am J Health Promot       Date:  2013 Mar-Apr

3.  Comparison of early-, late-, and non-participants in a school-based asthma management program for urban high school students.

Authors:  Christine L M Joseph; Jacquelyn Saltzgaber; Suzanne L Havstad; Christine C Johnson; Dayna Johnson; Edward L Peterson; Gwen Alexander; Mick P Couper; Dennis R Ownby
Journal:  Trials       Date:  2011-06-06       Impact factor: 2.279

4.  When is informed consent required in cluster randomized trials in health research?

Authors:  Andrew D McRae; Charles Weijer; Ariella Binik; Jeremy M Grimshaw; Robert Boruch; Jamie C Brehaut; Allan Donner; Martin P Eccles; Raphael Saginur; Angela White; Monica Taljaard
Journal:  Trials       Date:  2011-09-09       Impact factor: 2.279

5.  Changes to the law on consent in South Africa: implications for school-based adolescent sexual and reproductive health research.

Authors:  Melanie Zuch; Amanda J Mason-Jones; Catherine Mathews; Lesley Henley
Journal:  BMC Int Health Hum Rights       Date:  2012-04-10

6.  Does the use of passive or active consent affect consent or completion rates, or dietary data quality? Repeat cross-sectional survey among school children aged 11-12 years.

Authors:  Suzanne Spence; Martin White; Ashley J Adamson; John N S Matthews
Journal:  BMJ Open       Date:  2015-01-13       Impact factor: 2.692

7.  Challenges to obtaining parental permission for child participation in a school-based waterpipe tobacco smoking prevention intervention in Qatar.

Authors:  Rima T Nakkash; Ahmad Al Mulla; Lena Torossian; Roubina Karhily; Lama Shuayb; Ziyad R Mahfoud; Ibrahim Janahi; Al Anoud Al Ansari; Rema A Afifi
Journal:  BMC Med Ethics       Date:  2014-09-30       Impact factor: 2.652

8.  Challenges for consent and community engagement in the conduct of cluster randomized trial among school children in low income settings: experiences from Kenya.

Authors:  George Okello; Caroline Jones; Maureen Bonareri; Sarah N Ndegwa; Carlos McHaro; Juddy Kengo; Kevin Kinyua; Margaret M Dubeck; Katherine E Halliday; Matthew C H Jukes; Sassy Molyneux; Simon J Brooker
Journal:  Trials       Date:  2013-05-16       Impact factor: 2.279
  8 in total

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