NIH Privacy Act Memo

Attach_10_Privacy Act Letter 2019.pdf

The Clinical Trials Reporting Program (CTRP) Database (NCI)

NIH Privacy Act Memo

OMB: 0925-0600

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DATE:

August 9, 2019

TO:

Gisele Sarosy, MD
Coordinating Center for Clinical Trials (CCCT)
National Cancer Institute

FROM:

NIH Privacy Act Officer

SUBJECT: Applicability of the Privacy Act: “NCI Clinical Trials Reporting Program (CTRP)
Database”
I have reviewed the NCI submission to OMB which requests the approval of the CTRP database be
extended. The database serves as a single, definitive source of information about all clinical
interventional and observational research conducted at institutions that receive NCI funding,
including Cooperative Group trials, externally peer-reviewed trials, institutionally supported
investigator-initiated trials, and industry-sponsored studies.
The database provides a comprehensive real-time view of the state of the NCI-supported clinical
research, which enables NCI to make informed prioritization decisions via disease-specific steering
committees. The information stored in the CTRP database is collected to manage the portfolio,
comply with regulatory and administrative report obligations and disseminate appropriate cancer
research information to the public.
I have determined that the Privacy Act will not apply to this data collection. The database will store
study subject accrual information that is collected on a quarterly basis (i.e., race/ethnicity, date of
birth, gender and zip code). However, the database was not designed to retrieve information about
the study subject by a personal identifier. Although a study subject ID code will be assigned by the
individual trial site where a research subject or patient is accrued on a study, the code will be unique
to the study subject within the context of the specific protocol. The code will not replace any
individual identifier and cannot be derived from any information related to the individual. Further,
any key associated with the code will not be provided to NCI in order to re-identity research subjects
or patients.
The portions of the CTRP database that pertain to the description of clinical research projects and
summarized information on accrual will be publicly accessible. All non-public data will be maintained
in accordance with appropriate security access controls and limited to designated staff with a direct
business need. If you have questions, contact me at (301) 402-6201.

Celeste Dade-Vinson
NIH Privacy Act Officer
CC: Diane Kreinbrink, Office of Management Policy and Compliance, NCI


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