Publicaties
Co-creation with research participants to inform the design of electronic informed consent KU Leuven
Informed consent procedures in patients with an acute inability to provide informed consent Universiteit Antwerpen KU Leuven
Informed consent in the context of pharmacogenomic research: ethical considerations KU Leuven
Surgical informed consent in Iran-how much is it informed? KU Leuven
Relational ethics, informed consent, and informed assent in participatory research with children with complex communication needs Universiteit Gent Universiteit Antwerpen KU Leuven
Naming it 'nano' : expert views on 'nano' terminology in informed consent forms of first-in-human nanomedicine trials Universiteit Gent
Could the decision of trial participation precede the informed consent process? Evidence from Burkina Faso Instituut voor Tropische Geneeskunde Universiteit Gent KU Leuven Vrije Universiteit Brussel
BACKGROUND: Over the last years, the number of clinical trials carried out in low-income countries with poor medical infrastructure and limited access to health care has increased. In these settings, the decision of participating in a clinical study may be influenced by factors related to participants' vulnerability that limit the efficacy of the informed consent.
METHODS: A mixed methods social science study, based on the ...
Video-augmentation of the informed consent process in mental health research Vrije Universiteit Brussel
Only around 50-75% of individuals fully understand the various aspects of informed consent in research. The aim of our study was to examine whether supplementing the conventional paper-based informed consent process with an audiovisual aid improves participants' understanding of the informed consent process and the information conveyed to them. Participants from two mental health/substance use intervention development studies were recruited ...
Surgical informed consent in obstetric and gynecologic surgeries: experience from a comprehensive teaching hospital in Southern Ethiopia Instituut voor Tropische Geneeskunde
BACKGROUND: Surgical Informed Consent (SIC) has long been recognized as an important component of modern medicine. The ultimate goals of SIC are to improve clients' understanding of the intended procedure, increase client satisfaction, maintain trust between clients and health providers, and ultimately minimize litigation issues related to surgical procedures. The purpose of the current study is to assess the comprehensiveness of the SIC ...