“…All parents agreed that detailed information about the topic, including the benefits and possible harms, aims of the project, and research team qualifications and detailed contact information, should be provided. Previous studies have shown that providing enough clear information about the benefits, risks, and study procedures increased parental satisfaction (Kupst, Patenaude, Walco, & Sterling, 2003; Steven, Broadis, Carachi, & Brindley, 2008; Stolt, Helgesson, Liss, Svensson, & Ludvigsson, 2005) and enhanced enrollments of children in pediatric research, to include clinical studies (Bernhardt, Tambor, Fraser, Wissow, & Geller, 2003; Boccia, Campbell, Goldman, & Skinner, 2009; Eder, Yamokoski, Wittmann, & Kodish, 2007; van Stuijvenberg et al, 1998). It is strongly recommended that more studies be conducted on this aspect to evaluate the quality of the provided information and informed consent procedures when conducting pediatric and other types of research in Jordan and the Arabic region.…”