Abstract Background Very few researchers have reported on procedures of recruiting, obtaining informed consent, and compensating participants in health research in the Arabian Gulf Region. Empirical research can inform the debate about whether to adjust these procedures for culturally diverse settings. Our objective was to delineate procedures related to recruiting, obtaining informed consent, and compensating health research participants in the extremely high-density multicultural setting of Qatar. Methods During a multistage mixed methods project, field observations and qualitative interviews were conducted in a general medicine cl...
Background: To improve equity in access to medical research, successful strategies are needed to rec...
BACKGROUND: Explaining technical terms in consent forms prior to seeking informed consent to recruit...
Background: Rapid Ethical Assessment (REA) is a form of rapid ethnographic assessment conducted at t...
Abstract Background Health care researchers working i...
With the increasing number of universities in the Arab region, there has been a consequent increase ...
Ethical and legal dogmas mandated obtaining informed consent from the research participants and thei...
Informed consent requirements for conducting research with human participants are set by institution...
Recruitment into clinical research studies is a major challenge. This study was carried out to explo...
Background: Previous health research has often explicitly excluded individuals from minority ethni...
Introduction: Informed consent has been recognized as an important component of research protocols a...
Background Informed consent is a key component of bio-medical research involving human participan...
BACKGROUND: The doctrine of informed consent (IC) exists to protect individuals from exploitation or...
Western medicine is a fundamentally rational and experimental science. It holds research in high est...
Informed consent has become an essential element of human subject research. Certain components are e...
BACKGROUND: Commentators have expressed concern regarding the existence of proper ethics review syst...
Background: To improve equity in access to medical research, successful strategies are needed to rec...
BACKGROUND: Explaining technical terms in consent forms prior to seeking informed consent to recruit...
Background: Rapid Ethical Assessment (REA) is a form of rapid ethnographic assessment conducted at t...
Abstract Background Health care researchers working i...
With the increasing number of universities in the Arab region, there has been a consequent increase ...
Ethical and legal dogmas mandated obtaining informed consent from the research participants and thei...
Informed consent requirements for conducting research with human participants are set by institution...
Recruitment into clinical research studies is a major challenge. This study was carried out to explo...
Background: Previous health research has often explicitly excluded individuals from minority ethni...
Introduction: Informed consent has been recognized as an important component of research protocols a...
Background Informed consent is a key component of bio-medical research involving human participan...
BACKGROUND: The doctrine of informed consent (IC) exists to protect individuals from exploitation or...
Western medicine is a fundamentally rational and experimental science. It holds research in high est...
Informed consent has become an essential element of human subject research. Certain components are e...
BACKGROUND: Commentators have expressed concern regarding the existence of proper ethics review syst...
Background: To improve equity in access to medical research, successful strategies are needed to rec...
BACKGROUND: Explaining technical terms in consent forms prior to seeking informed consent to recruit...
Background: Rapid Ethical Assessment (REA) is a form of rapid ethnographic assessment conducted at t...