{"id":{"repo_id":"cape-town","oai_identifier":"oai:open.uct.ac.za:11427/9361"},"canonical_url":"https://search.dev.ndltd.org/etd/cape-town/oai:open.uct.ac.za:11427/9361","repository":{"repo_id":"cape-town","name":"University of Cape Town","base_url":"https://open.uct.ac.za/oai/request"},"display":{"title":"A quantitative evaluation of the quality of informed consent in a developing country setting","abstract":"Informed consent is an ethical and legal requirement for research involving human participants. However, there have been few studies that have evaluated the process, particularly in an African setting. In addition, standardized methods for assessing the quality of informed consent are not available in the literature. 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The aim of the study was to evaluate the quality of consent in a large tuberculosis vaccine immunology study and to identify factors associated with the quality of consent.","abstract_has_math":false,"creators":["Minnies, Deon"],"institution":"Department of Public Health and Family Medicine","degree_name":null,"degree_level":null,"degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":["Ehrlich, Rodney","Hawkridge, Anthony"],"committee_chairs":[],"committee_members":[],"year":2005,"date_issued":"2005","date_published":"2005","updated_at":"2026-07-22T22:23:05Z","subjects":[],"languages":["eng"],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/11427/9361","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Ehrlich, Rodney","Hawkridge, Anthony"]},{"key":"dc:creator","label":"Author","values":["Minnies, Deon"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2014-11-08T08:06:15Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2014-11-08T08:06:15Z"]},{"key":"dc:date.issued","label":"Date","values":["2005"]},{"key":"dc:publisher.department","label":"Dc Publisher Department","values":["Department of Public Health and Family Medicine"]},{"key":"dc:publisher.institution","label":"Dc Publisher Institution","values":["University of Cape Town"]},{"key":"dc:type","label":"Dc Type","values":["Master Thesis"]},{"key":"dc:type.qualificationlevel","label":"Dc Type Qualificationlevel","values":["Masters"]},{"key":"dc:type.qualificationname","label":"Dc Type Qualificationname","values":["MPH"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["eng"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/11427/9361"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["Includes bibliographical references (leaves 59-62)."]},{"key":"dc:description.abstract","label":"Abstract","values":["Informed consent is an ethical and legal requirement for research involving human participants. However, there have been few studies that have evaluated the process, particularly in an African setting. In addition, standardized methods for assessing the quality of informed consent are not available in the literature. The aim of the study was to evaluate the quality of consent in a large tuberculosis vaccine immunology study and to identify factors associated with the quality of consent."]},{"key":"dc:title","label":"Title","values":["A quantitative evaluation of the quality of informed consent in a developing country setting"]}]}],"canonical_facts":{"dc:contributor.advisor":["Ehrlich, Rodney","Hawkridge, Anthony"],"dc:creator":["Minnies, Deon"],"dc:date.accessioned":["2014-11-08T08:06:15Z"],"dc:date.available":["2014-11-08T08:06:15Z"],"dc:date.issued":["2005"],"dc:description":["Includes bibliographical references (leaves 59-62)."],"dc:description.abstract":["Informed consent is an ethical and legal requirement for research involving human participants. 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