Literature DB >> 20713534

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

Mona Nabulsi1, Yvette Khalil, Jihad Makhoul.   

Abstract

BACKGROUND: Paediatric clinical research faces unique challenges that compromise optimal recruitment of children into clinical trials. A main barrier to enrolment of children is parental misconceptions about the research process. In developing countries, there is a knowledge gap regarding parental perceptions of and attitudes towards their children's participation in clinical trials.
OBJECTIVE: To explore such perceptions and attitudes in Lebanese parents. STUDY
DESIGN: 33 in-depth interviews were conducted with parents with and without previous research experience. Interviews were tape-recorded, transcribed in colloquial Arabic, and later subjected to thematic analysis.
RESULTS: Benefit/risk ratio assessment was a major determinant of parental consent. Fear of adverse events or painful procedures in research was a recurring theme in most interviews. Whereas perception of direct benefit to the child, trust in the physician or institution, financial gains or having a positive previous experience in research facilitated consent, a complex informed consent form and misunderstanding of the term 'randomisation' hindered parental approval of participation.
CONCLUSION: Lebanese parents have perceptions of and attitudes towards children's participation in clinical trials that are similar to those reported from the industrialised world. Improving communication with parents and building trust between researchers and parents is important for successful recruitment. Investigators planning to conduct paediatric trials in developing countries need to simplify consent forms and devise new ways to explain randomisation.

Entities:  

Mesh:

Year:  2010        PMID: 20713534     DOI: 10.1136/jme.2010.035899

Source DB:  PubMed          Journal:  J Med Ethics        ISSN: 0306-6800            Impact factor:   2.903


  24 in total

1.  Tailoring information provision and consent processes to research contexts: the value of rapid assessments.

Authors:  Susan Bull; Bobbie Farsides; Fasil Tekola Ayele
Journal:  J Empir Res Hum Res Ethics       Date:  2012-02       Impact factor: 1.742

2.  Attitudes of Patients in Developing Countries Toward Participating in Clinical Trials: A Survey of Saudi Patients Attending Primary Health Care Services.

Authors:  Lateefa O Al-Dakhil; Reem Alanazy; Rakan E AlHamad; Hazem Al-Mandeel; Abdulaziz Alobaid
Journal:  Oman Med J       Date:  2016-07

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

Authors:  Omar F Khabour; Mahmoud A Alomari; Nihaya A Al-Sheyab
Journal:  J Empir Res Hum Res Ethics       Date:  2017-07-12       Impact factor: 1.742

4.  Primary caregivers' experience with the informed consent process in the paediatric emergency department: An interview-based qualitative study.

Authors:  Adonis Wazir; Ibrahim Sandokji; Morten Greaves; Rasha D Sawaya
Journal:  Paediatr Child Health       Date:  2021-04-03       Impact factor: 2.253

5.  Patients' attitudes and perceptions regarding research and their rights: a pilot survey study from the Middle East.

Authors:  Tamer Hifnawy; Samer Kobrosly; Hillary Edwards; Manal Anwar; Dalia Zahran; Henry Silverman
Journal:  East Mediterr Health J       Date:  2017-08-27       Impact factor: 1.628

6.  Views of adolescents and parents on pediatric research without the potential for clinical benefit.

Authors:  David Wendler; Emily Abdoler; Lori Wiener; Christine Grady
Journal:  Pediatrics       Date:  2012-09-10       Impact factor: 7.124

7.  Attitudes of dental patients towards participation in research.

Authors:  S Al-Amad; M Awad; H Silverman
Journal:  East Mediterr Health J       Date:  2014-03-13       Impact factor: 1.628

8.  Consent and community engagement in diverse research contexts.

Authors: 
Journal:  J Empir Res Hum Res Ethics       Date:  2013-10       Impact factor: 1.742

9.  Effect of child health status on parents' allowing children to participate in pediatric research.

Authors:  Jérémy Vanhelst; Ludovic Hardy; Dina Bert; Stéphane Duhem; Stéphanie Coopman; Christian Libersa; Dominique Deplanque; Frédéric Gottrand; Laurent Béghin
Journal:  BMC Med Ethics       Date:  2013-02-15       Impact factor: 2.652

10.  Main characteristics and participation rate of European adolescents included in the HELENA study.

Authors:  Laurent Béghin; Inge Huybrechts; German Vicente-Rodríguez; Stefaan De Henauw; Frédéric Gottrand; Marcela Gonzales-Gross; Jean Dallongeville; Michael Sjöström; Catherine Leclercq; Sabine Dietrich; Manuel Castillo; Maria Plada; Dénes Molnar; Mathilde Kersting; Chantal C Gilbert; Luis A Moreno
Journal:  Arch Public Health       Date:  2012-06-19
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