Sponsor Accrual of Investigative Add-On Sites

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dc.contributor.advisorGwirtz, Patricia A.
dc.contributor.committeeMemberMarwah, Heema
dc.contributor.committeeMemberGatch, Michael B.
dc.creatorArbov, Eli
dc.date.accessioned2019-08-22T19:30:46Z
dc.date.available2019-08-22T19:30:46Z
dc.date.issued2016-05-01
dc.date.submitted2016-08-05T09:06:06-07:00
dc.description.abstractMeeting enrollment goals in clinical research trials has become increasingly more difficult due to heightened regulations and more stringent study protocols. This practicum report explores some of the reasons why sponsors in clinical research trials occasionally need to enlist the aid of investigative add-on sites, and highlights some of the unique opportunities that are presented to prospective add-on sites. Advanced Care Research Centers (ACRC) Trial’s current involvement in a contraceptive study, as an investigative add-on site, provides this report with a case study, where observations and the analysis of enrollment data can appraise their success as an add-on site. Past trials are also assessed in order to supplement other themes raised in this discussion.
dc.format.mimetypeapplication/pdf
dc.identifier.urihttps://hdl.handle.net/20.500.12503/26025
dc.language.isoen
dc.provenance.legacyDownloads35
dc.subjectBehavior and Behavior Mechanisms
dc.subjectHealth Services Research
dc.subjectinvestigative add-on site
dc.subjectsecondary site
dc.subjectenrollment period
dc.titleSponsor Accrual of Investigative Add-On Sites
dc.typeInternship Practicum Report
dc.type.materialtext
thesis.degree.departmentGraduate School of Biomedical Sciences
thesis.degree.disciplineClinical Research Management
thesis.degree.grantorUniversity of North Texas Health Science Center at Fort Worth
thesis.degree.nameMaster of Science

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