Literature DB >> 28697643

Parental Perceptions About Informed Consent/Assent in Pediatric Research in Jordan.

Omar F Khabour1, Mahmoud A Alomari1, Nihaya A Al-Sheyab1,2.   

Abstract

The informed consent/assent process during enrollment in pediatric research is integral to protecting children from possible harm. Here we explored parents' perceptions about the informed consent/assent process in Jordan. Therefore, focus group interviews were conducted that focused on the importance of consent/assent, the quality of the information provided during consent process, and the parents' perceptions toward written/verbal informed consent. Content thematic analysis approach was adopted in the transcription and translation processes of the interviews. The majority of parents have an ethically acceptable understanding of many of the aspects related to consent/assent; however, some views were not consistent with the proper conduct of research. For example, some parents believed that informed consent is not required for questionnaire studies. Discrepancies were also noted regarding the appropriate age of a child's assent. Some parents would force their child to participate. Thus, the development of Jordanian, culturally sensitive pediatric research guidelines is required.

Entities:  

Keywords:  Jordan; Middle East; adolescent; assent; child; consent; parents

Mesh:

Year:  2017        PMID: 28697643      PMCID: PMC5595642          DOI: 10.1177/1556264617718937

Source DB:  PubMed          Journal:  J Empir Res Hum Res Ethics        ISSN: 1556-2646            Impact factor:   1.742


  36 in total

1.  Improving informed consent: suggestions from parents of children with leukemia.

Authors:  Michelle L Eder; Amy D Yamokoski; Peter W Wittmann; Eric D Kodish
Journal:  Pediatrics       Date:  2007-04       Impact factor: 7.124

2.  Confidentiality, informed consent, and children's participation in research involving stored tissue samples: interviews with medical professionals from the Middle East.

Authors:  Ghiath Alahmad; Mohammed Al Jumah; Kris Dierickx
Journal:  Narrat Inq Bioeth       Date:  2015

3.  Parental attitudes towards and perceptions of their children's participation in clinical research: a developing-country perspective.

Authors:  Mona Nabulsi; Yvette Khalil; Jihad Makhoul
Journal:  J Med Ethics       Date:  2010-08-16       Impact factor: 2.903

Review 4.  Clinical trials in children.

Authors:  Pathma D Joseph; Jonathan C Craig; Patrina H Y Caldwell
Journal:  Br J Clin Pharmacol       Date:  2015-03       Impact factor: 4.335

5.  Perceptions of African-American health professionals and community members on the participation of children and pregnant women in genetic research.

Authors:  E M Ngui; T D Warner; L W Roberts
Journal:  Public Health Genomics       Date:  2013-11-06       Impact factor: 2.000

Review 6.  Informed consent/assent in children. Statement of the Ethics Working Group of the Confederation of European Specialists in Paediatrics (CESP).

Authors:  Maria De Lourdes Levy; Victor Larcher; Ronald Kurz
Journal:  Eur J Pediatr       Date:  2003-07-19       Impact factor: 3.183

7.  Sign on the dotted line: parental consent.

Authors:  Mairi Steven; Emily Broadis; Robert Carachi; Nicola Brindley
Journal:  Pediatr Surg Int       Date:  2008-05-28       Impact factor: 1.827

8.  Parents' and children's attitudes toward the enrollment of minors in genetic susceptibility research: implications for informed consent.

Authors:  Barbara A Bernhardt; Ellen S Tambor; Gertrude Fraser; Lawrence S Wissow; Gail Geller
Journal:  Am J Med Genet A       Date:  2003-02-01       Impact factor: 2.802

9.  Components and public health impact of population growth in the Arab world.

Authors:  Asharaf Abdul Salam; Ibrahim Elsegaey; Rshood Khraif; Abdullah AlMutairi; Ali Aldosari
Journal:  PLoS One       Date:  2015-05-18       Impact factor: 3.240

Review 10.  A New Ethical Challenge for Institutional Review Boards (IRBs)/Ethics Committees (ECs) in the Assessment of Pediatric Clinical Trials.

Authors:  Klaus Rose; Hans Kummer
Journal:  Children (Basel)       Date:  2015-05-28
View more
  7 in total

1.  Motivators and barriers towards clinical research participation: A population-based survey from an Arab MENA country.

Authors:  Kamal M Al-Shami; Wesam S Ahmed; Karem H Alzoubi
Journal:  PLoS One       Date:  2022-06-24       Impact factor: 3.752

2.  Perceptions Towards Medical Research Participation: A Study from Jordan.

Authors:  Rana Abu Farha; Karem Alzoubi; Omar Khabour; Tareq Mukattash
Journal:  J Multidiscip Healthc       Date:  2020-09-14

3.  How should assent to research be sought in low income settings? Perspectives from parents and children in Southern Malawi.

Authors:  Helen Mangochi; Kate Gooding; Aisleen Bennett; Michael Parker; Nicola Desmond; Susan Bull
Journal:  BMC Med Ethics       Date:  2019-05-14       Impact factor: 2.652

4.  Cultural considerations for informed consent in paediatric research in low/middle-income countries: a scoping review.

Authors:  Marcela Colom; Peter Rohloff
Journal:  BMJ Paediatr Open       Date:  2018-12-05

5.  Bioethical reflexivity and requirements of valid consent: conceptual tools.

Authors:  John Barugahare
Journal:  BMC Med Ethics       Date:  2019-07-04       Impact factor: 2.652

6.  The understanding of research ethics at health sciences schools in Jordan: a cross-sectional study.

Authors:  Nafez Abu Tarboush; Zaid Alkayed; Karem H Alzoubi; Wael K Al-Delaimy
Journal:  BMC Med Educ       Date:  2020-04-21       Impact factor: 2.463

7.  Biomedical Data Sharing Among Researchers: A Study from Jordan.

Authors:  Lina Al-Ebbini; Omar F Khabour; Karem H Alzoubi; Almuthanna K Alkaraki
Journal:  J Multidiscip Healthc       Date:  2020-11-23
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.