BACKGROUND Understanding local contextual factors is important when conducting international collaborative studies in low-income country settings. Rapid ethical assessment (a brief qualitative intervention designed to map the ethical terrain of a research setting prior to recruitment of participants), has been used in a range of research-naïve settings. We used rapid ethical assessment to explore ethical issues and challenges associated with approaching communities and gaining informed consent in North West Cameroon. METHODS This qualitative study was carried out in two health districts in the North West Region of Cameroon between February and April 2012. Eleven focus group discussions (with a total of 107 participants) were carrie...
ABSTRACT: guidance requires that consent processes for research be appropriately tailored to their c...
In our research unit on the Kenyan Coast, parents sign consent for over 4000 children to be involved...
Objective: To identify and highlight challenges related to informed consent process for clinical tri...
Background Informed consent is a key component of bio-medical research involving human participan...
Background: Rapid Ethical Assessment (REA) is a form of rapid ethnographic assessment conducted at t...
Background International collaborators face challenges in the design and implementation of ethical ...
BACKGROUND There is limited assessment of whether research participants in low-income settings ar...
Involving vulnerable pediatric populations in international research requires culturally appropriate...
BACKGROUND: Currently there is increasing recognition of the need for research in developing countri...
Currently there is increasing recognition of the need for research in developing countries where dis...
Abstract Background Researchers conducting community-based participatory action research (CBPAR) in ...
This article argues that localizing access – a general ethical principle – is a workable strategy th...
Objective: To identify and highlight challenges related to informed consent processfor clinical tria...
Individual informed consent is a key ethical obligation for clinical studies, but empirical studies ...
Individual informed consent is a key ethical obligation for clinical studies, but empirical studies ...
ABSTRACT: guidance requires that consent processes for research be appropriately tailored to their c...
In our research unit on the Kenyan Coast, parents sign consent for over 4000 children to be involved...
Objective: To identify and highlight challenges related to informed consent process for clinical tri...
Background Informed consent is a key component of bio-medical research involving human participan...
Background: Rapid Ethical Assessment (REA) is a form of rapid ethnographic assessment conducted at t...
Background International collaborators face challenges in the design and implementation of ethical ...
BACKGROUND There is limited assessment of whether research participants in low-income settings ar...
Involving vulnerable pediatric populations in international research requires culturally appropriate...
BACKGROUND: Currently there is increasing recognition of the need for research in developing countri...
Currently there is increasing recognition of the need for research in developing countries where dis...
Abstract Background Researchers conducting community-based participatory action research (CBPAR) in ...
This article argues that localizing access – a general ethical principle – is a workable strategy th...
Objective: To identify and highlight challenges related to informed consent processfor clinical tria...
Individual informed consent is a key ethical obligation for clinical studies, but empirical studies ...
Individual informed consent is a key ethical obligation for clinical studies, but empirical studies ...
ABSTRACT: guidance requires that consent processes for research be appropriately tailored to their c...
In our research unit on the Kenyan Coast, parents sign consent for over 4000 children to be involved...
Objective: To identify and highlight challenges related to informed consent process for clinical tri...