Informed Consent in Health Research: Challenges and Barriers in Low-and Middle-Income Countries with Specific Reference to Nepal
Authors: Regmi, P.R., Aryal, N., Kurmi, O., Pant, P.R., van Teijlingen, E. and Wasti, S.P.
Journal: Developing World Bioethics
Volume: 17
Issue: 2
Pages: 84-89
eISSN: 1471-8847
ISSN: 1471-8731
DOI: 10.1111/dewb.12123
Abstract:Obtaining ‘informed consent’ from every individual participant involved in health research is a mandatory ethical practice. Informed consent is a process whereby potential participants are genuinely informed about their role, risk and rights before they are enrolled in the study. Thus, ethics committees in most countries require ‘informed consent form’ as part of an ethics application which is reviewed before granting research ethics approval. Despite a significant increase in health research activity in low-and middle-income countries (LMICs) in recent years, only limited work has been done to address ethical concerns. Most ethics committees in LMICs lack the authority and/or the capacity to monitor research in the field. This is important since not all research, particularly in LMICs region, complies with ethical principles, sometimes this is inadvertently or due to a lack of awareness of their importance in assuring proper research governance. With several examples from Nepal, this paper reflects on the steps required to obtain informed consents and highlights some of the major challenges and barriers to seeking informed consent from research participants. At the end of this paper, we also offer some recommendations around how can we can promote and implement optimal informed consent taking process. We believe that paper is useful for researchers and members of ethical review boards in highlighting key issues around informed consent.
https://eprints.bournemouth.ac.uk/24506/
Source: Scopus
Informed Consent in Health Research: Challenges and Barriers in Low-and Middle-Income Countries with Specific Reference to Nepal.
Authors: Regmi, P.R., Aryal, N., Kurmi, O., Pant, P.R., van Teijlingen, E. and Wasti, S.P.
Journal: Dev World Bioeth
Volume: 17
Issue: 2
Pages: 84-89
eISSN: 1471-8847
DOI: 10.1111/dewb.12123
Abstract:Obtaining 'informed consent' from every individual participant involved in health research is a mandatory ethical practice. Informed consent is a process whereby potential participants are genuinely informed about their role, risk and rights before they are enrolled in the study. Thus, ethics committees in most countries require 'informed consent form' as part of an ethics application which is reviewed before granting research ethics approval. Despite a significant increase in health research activity in low-and middle-income countries (LMICs) in recent years, only limited work has been done to address ethical concerns. Most ethics committees in LMICs lack the authority and/or the capacity to monitor research in the field. This is important since not all research, particularly in LMICs region, complies with ethical principles, sometimes this is inadvertently or due to a lack of awareness of their importance in assuring proper research governance. With several examples from Nepal, this paper reflects on the steps required to obtain informed consents and highlights some of the major challenges and barriers to seeking informed consent from research participants. At the end of this paper, we also offer some recommendations around how can we can promote and implement optimal informed consent taking process. We believe that paper is useful for researchers and members of ethical review boards in highlighting key issues around informed consent.
https://eprints.bournemouth.ac.uk/24506/
Source: PubMed
Informed Consent in Health Research: Challenges and Barriers in Low-and Middle-Income Countries with Specific Reference to Nepal
Authors: Regmi, P.R., Aryal, N., Kurmi, O., Pant, P.R., van Teijlingen, E. and Wasti, S.P.
Journal: DEVELOPING WORLD BIOETHICS
Volume: 17
Issue: 2
Pages: 84-89
eISSN: 1471-8847
ISSN: 1471-8731
DOI: 10.1111/dewb.12123
https://eprints.bournemouth.ac.uk/24506/
Source: Web of Science (Lite)
Informed consent in health research: challenges and barriers in low-and middle-income countries with specific reference to Nepal
Authors: Regmi, P., Aryal, N., kurmi, O., Pant, P., van Teijlingen, E. and Wasti, S.
Journal: Developing World Bioethics
Publisher: http://onlinelibrary.wiley.com/doi/10.1111/dewb.12123/full
ISSN: 1471-8847
Abstract:Obtaining ‘informed consent’ from every individual participant involved in health research is a mandatory ethical practice. Informed consent is a process whereby potential participants are genuinely informed about their role, risk and rights before they are enrolled in the study. Thus, ethics committees in most countries require ‘informed consent form’ as part of an ethics application which is reviewed before granting research ethics approval. Despite a significant increase in health research activity in low-and middle-income countries (LMICs) in recent years, only limited work has been done to address ethical concerns. Most ethics committees in LMICs lack the authority and/or the capacity to monitor research in the field. This is important since not all research, particularly in LMICs region, complies with ethical principles, sometimes this is inadvertently or due to a lack of awareness of their importance in assuring proper research governance. With several examples from Nepal, this paper reflects on the steps required to obtain informed consents and highlights some of the major challenges and barriers to seeking informed consent from research participants. At the end of this paper, we also offer some recommendations around how can we can promote and implement optimal informed consent taking process. We believe that paper is useful for researchers and members of ethical review boards in highlighting key issues around informed consent.
https://eprints.bournemouth.ac.uk/24506/
http://onlinelibrary.wiley.com/doi/10.1111/dewb.12123/full
Source: Manual
Informed Consent in Health Research: Challenges and Barriers in Low-and Middle-Income Countries with Specific Reference to Nepal.
Authors: Regmi, P.R., Aryal, N., Kurmi, O., Pant, P.R., van Teijlingen, E. and Wasti, S.P.
Journal: Developing world bioethics
Volume: 17
Issue: 2
Pages: 84-89
eISSN: 1471-8847
ISSN: 1471-8731
DOI: 10.1111/dewb.12123
Abstract:Obtaining 'informed consent' from every individual participant involved in health research is a mandatory ethical practice. Informed consent is a process whereby potential participants are genuinely informed about their role, risk and rights before they are enrolled in the study. Thus, ethics committees in most countries require 'informed consent form' as part of an ethics application which is reviewed before granting research ethics approval. Despite a significant increase in health research activity in low-and middle-income countries (LMICs) in recent years, only limited work has been done to address ethical concerns. Most ethics committees in LMICs lack the authority and/or the capacity to monitor research in the field. This is important since not all research, particularly in LMICs region, complies with ethical principles, sometimes this is inadvertently or due to a lack of awareness of their importance in assuring proper research governance. With several examples from Nepal, this paper reflects on the steps required to obtain informed consents and highlights some of the major challenges and barriers to seeking informed consent from research participants. At the end of this paper, we also offer some recommendations around how can we can promote and implement optimal informed consent taking process. We believe that paper is useful for researchers and members of ethical review boards in highlighting key issues around informed consent.
https://eprints.bournemouth.ac.uk/24506/
Source: Europe PubMed Central
Informed consent in health research: challenges and barriers in low-and middle-income countries with specific reference to Nepal
Authors: Regmi, P., Aryal, N., Kurmi, O., Pant, P., van Teijlingen, E. and Wasti, S.P.
Journal: Developing World Bioethics
Volume: 17
Issue: 2
Pages: 84-89
ISSN: 1471-8847
Abstract:Obtaining 'informed consent' from every individual participant involved in health research is a mandatory ethical practice. Informed consent is a process whereby potential participants are genuinely informed about their role, risk and rights before they are enrolled in the study. Thus, ethics committees in most countries require 'informed consent form' as part of an ethics application which is reviewed before granting research ethics approval. Despite a significant increase in health research activity in low-and middle-income countries (LMICs) in recent years, only limited work has been done to address ethical concerns. Most ethics committees in LMICs lack the authority and/or the capacity to monitor research in the field. This is important since not all research, particularly in LMICs region, complies with ethical principles, sometimes this is inadvertently or due to a lack of awareness of their importance in assuring proper research governance. With several examples from Nepal, this paper reflects on the steps required to obtain informed consents and highlights some of the major challenges and barriers to seeking informed consent from research participants. At the end of this paper, we also offer some recommendations around how can we can promote and implement optimal informed consent taking process. We believe that paper is useful for researchers and members of ethical review boards in highlighting key issues around informed consent.
https://eprints.bournemouth.ac.uk/24506/
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1471-8847
Source: BURO EPrints