Clinical investigators are disappearing from the ranks of federally funded research portfolios to the extent that they have become an """"""""endangered species"""""""". To counter this loss, the Training Program in Human Investigation at Thomas Jefferson University prepares investigators for enduring careers pursuing funded hypothesis-driven patient-oriented research and to be role models and mentors to subsequent investigators pursuing similar careers. This Clinical Research Curriculum is composed of a multi-disciplinary faculty with expertise in patient-oriented research, a core of relevant courses and patient-based research experiences, and mentored training in clinical investigation. Successful completion of the program requires >40 course credits and a formal research thesis and defense. Applications are solicited from a large pool (>650) of trainees drawn from different colleges within the university, as well as from clinical training programs at other health care centers in Philadelphia. Eligible applicants include house officers and subspecialty fellows, dentists, pharmacy fellows with a Pharm.D., Ph.D. fellows, and those with a doctoral degree in nursing interested in patient-oriented research. Applicants submit a written application, three letters of recommendation, and transcripts and are selected by an Advisory Committee following personal interviews. Once accepted, trainees pursue a unique program of didactic and applied research components. Formal coursework provides training in essential topics for patient-oriented research including biostatistics, epidemiology, clinical trial design, database management, outcomes research, bioethics and the responsible conduct of research, clinical pharmacology, federal policy and regulations regarding human subjects, scientific writing and grant writing. Coursework is supplemented with components that provide practical experience central to the conduct of patient-oriented research. These include (1) a clerkship in the Jefferson Clinical Research Unit in which trainees participate in a mentored clinical research experience by generating, implementing, completing, and reporting on a randomized clinical trial; and (2) identification of an interest-specific thesis question and advisor, development of a thesis proposal, and conduct of thesis research. Additional novel aspects of this training program include rotations on the Institutional Review Board (IRB) and/or Cancer Clinical Research Review Committee (CCRRC) and a clerkship in the critical review of scientific literature with the editorial staff of the Annals of Internal Medicine. Other important programmatic components include ethics seminars and conferences, journal club in clinical investigation, an in-house research seminar series, and seminars in clinical investigation with invited speakers from outside the institution. Upon completion of the program, trainees have (1) a thorough understanding of hypothesis formulation and testing in patient-based studies, (2) a theoretical foundation and working knowledge of research designs, (3) insight into the integration of laboratory-based analyses and surrogate endpoints in patient-oriented research, (4) a demonstrated record of achievement conducting randomized clinical trials and other types of studies documented through publication, (5) the ability to critically evaluate the scientific literature, and (6) the ability to employ various computer-based statistical and database packages in research-related. Upon completion of the program, trainees are qualified to perform independent clinical research with certification through a Master's of Science in Human Investigation.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Clinical Research Curriculum Award (CRCA) (K30)
Project #
9K30RR022299-06
Application #
6846522
Study Section
Special Emphasis Panel (ZHL1-CSR-R (O1))
Program Officer
Wilde, David B
Project Start
2000-09-30
Project End
2010-06-30
Budget Start
2005-09-27
Budget End
2006-06-30
Support Year
6
Fiscal Year
2005
Total Cost
$300,000
Indirect Cost
Name
Thomas Jefferson University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
053284659
City
Philadelphia
State
PA
Country
United States
Zip Code
19107
Lin, Jieru E; Colon-Gonzalez, Francheska; Blomain, Erik et al. (2016) Obesity-Induced Colorectal Cancer Is Driven by Caloric Silencing of the Guanylin-GUCY2C Paracrine Signaling Axis. Cancer Res 76:339-46
Wilson, Chantell; Lin, Jieru E; Li, Peng et al. (2014) The paracrine hormone for the GUCY2C tumor suppressor, guanylin, is universally lost in colorectal cancer. Cancer Epidemiol Biomarkers Prev 23:2328-37
Gibbons, Ahmara V; Lin, Jieru E; Kim, Gilbert W et al. (2013) Intestinal GUCY2C prevents TGF-? secretion coordinating desmoplasia and hyperproliferation in colorectal cancer. Cancer Res 73:6654-66
Kupetsky-Rincon, E A; Kraft, W K (2012) Healthy volunteer registries and ethical research principles. Clin Pharmacol Ther 91:965-8
Mejia, Alex; Schulz, Stephanie; Hyslop, Terry et al. (2012) Molecular staging individualizing cancer management. J Surg Oncol 105:468-74
Gong, Jian P; Schulz, Stephanie; Hyslop, Terry et al. (2012) GUCY2C molecular staging personalizes colorectal cancer patient management. Biomark Med 6:339-48
Kim, Gilbert W; Lin, Jieru E; Valentino, Michael A et al. (2011) Regulation of appetite to treat obesity. Expert Rev Clin Pharmacol 4:243-59
Valentino, Michael A; Colon-Gonzalez, Francheska; Lin, Jieru E et al. (2010) Current trends in targeting the hormonal regulation of appetite and energy balance to treat obesity. Expert Rev Endocrinol Metab 5:765-783
Mejia, Alex; Schulz, Stephanie; Hyslop, Terry et al. (2009) GUCY2C reverse transcriptase PCR to stage pN0 colorectal cancer patients. Expert Rev Mol Diagn 9:777-85
Mejia, Alex; Waldmana, Scott A (2008) Previstage GCC test for staging patients with colorectal cancer. Expert Rev Mol Diagn 8:571-8