2. Clinical Trial Subject Database Registry
About Princeton Medical
Institute
• CNS clinical research site
• Private Psychiatry Office
• Over 1,000 subjects enrolled
in clinical trials
Significance
Methods
EvaluationPurpose
Acknowledgements
• Subjects read IRB approved ICF
• Details information used for
database
• Information was added if subject
gave consent
• No penalty for non-compliance
• Register participants from
Princeton site
• Reduce duplicity in clinical trails
• Duplicity in trials contributes to
failure
• Patients become “Professional
Subjects”
• Communication between sites is
key
• CTS database allows
communication
• Rates of compliance determined
success
• Rate of non-compliance differed
based on delivery method
• 57% non-compliance rate among
subjects given ICF by the receptionist
• Greater compliance when ICF was
discussed with Study Coordinator
Special thanks to the Rutgers Internship
Seminar staff, as well as Dr. Apter, and the
other staff members at Princeton Medical
Institute.
Image credit: flickr user Paul-W
7
4
Outcomes
Consent Given No Consent Givenn=11
By Gabrielle Griffin
Delivery
Method
Number
Complied
Total
Given
ICF
Compliance
Rate
Receptionist 3 7 42.80%
Study
Coordinator 4 4 100%
Compliance and Methods
Total registered: 7
Image credit: flickr user Scott & White Healthcare
