Literature DB >> 15825977

The informed consent process in a cross-cultural setting: is the process achieving the intended result?

Melvina McCabe1, Frank Morgan, Helen Curley, Rick Begay, Dorothy M Gohdes.   

Abstract

This report is based on the experiences of Navajo interpreters working in a diabetes clinical trial and describes the problems encountered in translating the standard research consent across cultural and linguistic barriers. The interpreters and a Navajo language consultant developed a translation of the standard consent form, maintaining the sequence of information and exactly translating English words and phrases. After four months of using the translated consent, the interpreters met with the language expert and a diabetes expert to review their experiences in presenting the translation in the initial phases of recruitment. Their experiences suggest that the consent process often leads to embarrassment, confusion, and misperceptions that promoted mistrust. The formal processes that have been mandated to protect human subjects may create barriers to research in cross-cultural settings and may discourage participation unless sufficient attention is given to ensuring that both translations and cross-cultural communications are effective.

Entities:  

Keywords:  Biomedical and Behavioral Research; Empirical Approach

Mesh:

Year:  2005        PMID: 15825977

Source DB:  PubMed          Journal:  Ethn Dis        ISSN: 1049-510X            Impact factor:   1.847


  15 in total

1.  Responsibilities and obligations of using human research specimens transported across national boundaries.

Authors:  A S Muula; J M Mfutso-Bengo
Journal:  J Med Ethics       Date:  2007-01       Impact factor: 2.903

Review 2.  Seeking consent for research with indigenous communities: a systematic review.

Authors:  Emily F M Fitzpatrick; Alexandra L C Martiniuk; Heather D'Antoine; June Oscar; Maureen Carter; Elizabeth J Elliott
Journal:  BMC Med Ethics       Date:  2016-10-22       Impact factor: 2.652

Review 3.  Primary Outcome Measures in Pediatric Septic Shock Trials: A Systematic Review.

Authors:  Kusum Menon; James Dayre McNally; Jerry J Zimmerman; Michael S D Agus; Katie O'Hearn; R Scott Watson; Hector R Wong; Mark Duffett; David Wypij; Karen Choong
Journal:  Pediatr Crit Care Med       Date:  2017-03       Impact factor: 3.624

4.  Survey on Using Ethical Principles in Environmental Field Research with Place-Based Communities.

Authors:  Dianne Quigley; Alana Levine; David A Sonnenfeld; Phil Brown; Qing Tian; Xiaofan Wei
Journal:  Sci Eng Ethics       Date:  2018-01-03       Impact factor: 3.525

5.  Theory and practice of informed consent in the Czech Republic.

Authors:  Eva Krizova; Jiri Simek
Journal:  J Med Ethics       Date:  2007-05       Impact factor: 2.903

6.  How US institutional review boards decide when researchers need to translate studies.

Authors:  Robert Klitzman
Journal:  J Med Ethics       Date:  2013-03-08       Impact factor: 2.903

7.  Ensuring cross-cultural equivalence in translation of research consents and clinical documents: a systematic process for translating English to Chinese.

Authors:  Cheng-Chih Lee; Denise Li; Shoshana Arai; Kathleen Puntillo
Journal:  J Transcult Nurs       Date:  2008-10-23       Impact factor: 1.959

Review 8.  Research governance: ethical issues.

Authors:  Anne Slowther; Petra Boynton; Sara Shaw
Journal:  J R Soc Med       Date:  2006-02       Impact factor: 18.000

9.  Repeated assessments of informed consent comprehension among HIV-infected participants of a three-year clinical trial in Botswana.

Authors:  Lelia H Chaisson; Nancy E Kass; Bafanana Chengeta; Unami Mathebula; Taraz Samandari
Journal:  PLoS One       Date:  2011-10-27       Impact factor: 3.240

10.  Are good intentions good enough? Informed consent without trained interpreters.

Authors:  Linda M Hunt; Katherine B de Voogd
Journal:  J Gen Intern Med       Date:  2007-03-02       Impact factor: 5.128

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