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Att 5b_PIA
ICR 202003-0920-013 · OMB 0920-1284 · Object 99575701.
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Save Privacy Impact Assessment Form v 1.21 Status Form Number Form Date Question Answer 1 OPDIV: CDC 2 PIA Unique Identifier: 0920-19BG 2a Name: 11/16/2018 Web-based Approaches to Reach Black or African American and General Support System (GSS) Major Application 3 Minor Application (stand-alone) The subject of this PIA is which of the following? Minor Application (child) Electronic Information Collection Unknown 3a Identify the Enterprise Performance Lifecycle Phase of the system. Initiation Yes 3b Is this a FISMA-Reportable system? 4 Does the system include a Website or online application available to and for the use of the general public? 5 Identify the operator. 6 Point of Contact (POC): 7 Is this a new or existing system? 8 Does the system have Security Authorization (SA)? No Yes No Agency Contractor POC Title Project Officer POC Name Robin MacGowan POC Organization NCHHSTP/DHPIRS/PRB POC Email rjm3@cdc.gov POC Phone 404-639-1920 New Existing Yes No 8b Planned Date of Security Authorization Not Applicable Page 1 of 8 Save 8c Briefly explain why security authorization is not required Not applicable. 10 Describe in further detail any changes to the system that have occurred since the last PIA. Not applicable. 11 Describe the purpose of the system. The purpose of this information collection is to assess the effectiveness of mailing out rapid Human Immunodeficiency Virus (HIV) self-testing kits and providing access to Internetbased prevention mobile applications and websites as a public health strategy for increasing Black and Hispanic/Latino men who have sex with men (MSM) linkage to appropriate prevention and care services. Personally identifiable information (PII) including name, E-mail Address, Phone Number, Mailing Address, Military Status, Date Describe the type of information the system will of Birth, Employment Status, Age, Race/Ethnicity, City/Zip collect, maintain (store), or share. (Subsequent Code, Sex, Sex at Birth, Sexual Orientation, Education Level, 12 questions will identify if this information is PII and ask and Annual Income Information will be collected. about the specific data elements.) Respondents also will receive unique identification nonidentifiable codes. Provide an overview of the system and describe the 13 information it will collect, maintain (store), or share, either permanently or temporarily. All collected, maintained, and shared PII will be used to mail HIV testing kits and ensure receipt of those kits. PII will also allow study staff and partners to contact study participants for video counseling and other supportive services. Yes 14 Does the system collect, maintain, use or share PII? 15 Indicate the type of PII that the system will collect or maintain. No Social Security Number Date of Birth Name Photographic Identifiers Driver's License Number Biometric Identifiers Mother's Maiden Name Vehicle Identifiers E-Mail Address Mailing Address Phone Numbers Medical Records Number Medical Notes Financial Account Info Certificates Legal Documents Education Records Device Identifiers Military Status Employment Status Foreign Activities Passport Number Taxpayer ID City/Zip Code Age Sex/Sex at Birth Race/Ethnicity Sexual Orientation, Education Level, Annual income Information Page 2 of 8 Save Employees Public Citizens 16 Indicate the categories of individuals about whom PII is collected, maintained or shared. Business Partners/Contacts (Federal, state, local agencies) Vendors/Suppliers/Contractors Patients Other 17 How many individuals' PII is in the system? 18 For what primary purpose is the PII used? 19 Describe the secondary uses for which the PII will be used (e.g. testing, training or research) 500-4,999 PII data will be used to determine eligibility for this study. PII data also will be used to maintain contact with participants once enrolled in the study, mail out HIV testing kits, schedule and conduct follow-up HIV video counseling, and initiate participants engagement with the health Mpowerment website. 20 Describe the function of the SSN. Not applicable. 20a Cite the legal authority to use the SSN. Not applicable. Public Health Service Act, Section 301, "Research and Identify legal authorities governing information use Investigation," (42 U.S.C. 241); and Sections 304, 306 and 308(d) 21 which discuss authority to maintain data and provide and disclosure specific to the system and program. assurances of confidentiality for health research and related activities (42 U.S.C. 242 b, k, and m(d)). 22 Yes Are records on the system retrieved by one or more PII data elements? No Published: Identify the number and title of the Privacy Act System of Records Notice (SORN) that is being used 22a to cover the system or identify if a SORN is being developed. SORN 09-20-0160, "Records of Subjects in Health Published: Published: In Progress Page 3 of 8 Save Directly from an individual about whom the information pertains In-Person Hard Copy: Mail/Fax Email Online Other Government Sources 23 Within the OPDIV Other HHS OPDIV State/Local/Tribal Foreign Other Federal Entities Other Identify the sources of PII in the system. Non-Government Sources Members of the Public Commercial Data Broker Public Media/Internet Private Sector Other 23a Identify the OMB information collection approval number and expiration date. To be determined. Yes 24 Is the PII shared with other organizations? No Within HHS Identify with whom the PII is shared or disclosed and 24a for what purpose. Other Federal Agency/Agencies State or Local PII will be shared or disclosed in acco Agency/Agencies Private Sector Describe any agreements in place that authorizes the information sharing or disclosure (e.g. Computer 24b Matching Agreement, Memorandum of Understanding (MOU), or Information Sharing Agreement (ISA)). 24c Describe the procedures for accounting for disclosures PII will be shared or disclosed with other study sites hosted by An MOU, signed by Emory University, the University of North Carolina--Chapel Hill, and the University of Michigan, authorizes data and information sharing for the purposes of this study. Not applicable. Page 4 of 8 Save Describe the process in place to notify individuals 25 that their personal information will be collected. If no prior notice is given, explain the reason. 26 At the beginning of the study eligible participants will be asked to review and electronically sign a study consent form that informs participants that personal identifying information will be collected and every effort will be made to keep this information confidential. The consent form will include an explanation of the study, risks and benefits of participation, duration of participation, contact information for individuals who can answer questions about the research study regarding participant rights and protections, the voluntary nature of participation, and the right to withdraw without penalty. Participant are provided with information to contact study staff if clarification is needed regarding consent processes. Voluntary Is the submission of PII by individuals voluntary or mandatory? Mandatory Describe the method for individuals to opt-out of the Participants can opt out of all PII questions that are not collection or use of their PII. If there is no option to 27 eligibility related. Also, participants can opt out of participating object to the information collection, provide a in the study altogether or withdraw from the study at any time. reason. Describe the process to notify and obtain consent from the individuals whose PII is in the system when major changes occur to the system (e.g., disclosure 28 and/or data uses have changed since the notice at the time of original collection). Alternatively, describe why they cannot be notified or have their consent obtained. All participants will be allowed to track study progress and to correspond with study management if any changes are made to the system. They will be able to contact the Emory study team or the Emory Institutional Review Board (IRB). Study participants will be provided contact information and instruction to contact either the grantee principal investigators as well as the Emory human subjects staff if they have any questions about their rights as a participant or concerns that their PII may have been inappropriately obtained, used, or disclosed: Describe the process in place to resolve an individual's concerns when they believe their PII has 29 been inappropriately obtained, used, or disclosed, or that the PII is inaccurate. If no process exists, explain Emory IRB 404-712-0720 or 877-503-9797 why not. irb@emory.edu Emory Study Team 404-727-4340 iSTAMP@emory.edu Describe the process in place for periodic reviews of PII contained in the system to ensure the data's 30 integrity, availability, accuracy and relevancy. If no processes are in place, explain why not. Participants will be able to update PII at each interval of study participation when filling out surveys for data collection purposes. Users Administrators 31 Identify who will have access to the PII in the system and the reason why they require access. Study site administrators will have access to PII to contact study Developers Contractors Others Study staff assisting administrators may also have limited access to PII in Page 5 of 8 Save The ability to designate specific roles in Emory's digital study software allows users to control permissions and accessibility to participant information. Staff accessing the system will be Describe the procedures in place to determine which limited by which PII data is necessary to perform the duties of 32 system users (administrators, developers, their position. Users also are limited to a reporting-only role, contractors, etc.) may access PII. allowing for study oversight through real-time aggregate reporting, but no access to protected health information (PHI). The Centers for Disease Control and Prevention (CDC) lacks access to these data. Describe the methods in place to allow those with 33 access to PII to only access the minimum amount of information necessary to perform their job. Access to Sensitive PII will be restricted to individuals trained in human subject protections. PII is collected for a specific and identifiable purpose with access restricted to specific job tasks and individuals who perform those tasks. Assigned user permissions will be determined by their roles to perform different actions and need to view PII. Identify training and awareness provided to personnel (system owners, managers, operators, contractors and/or program managers) using the 34 system to make them aware of their responsibilities for protecting the information being collected and maintained. All research personnel employed by Emory and subcontractors under this contract will have completed Collaborative Institutional Training Initiative (CITI) training before they are permitted to participate in research or view PII. All study staff will be trained on relevant study procedures prior to interacting with participants involved in study activities. Describe training system users receive (above and 35 beyond general security and privacy awareness training). Emory researchers and study staff will participate in internal training on study instruments, procedures, and reporting regulations, which includes privacy awareness and confidentiality training. Graduate research assistants also must sign a code of conduct to ensure participants' safety and privacy. Do contracts include Federal Acquisition Regulation 36 and other appropriate clauses ensuring adherence to privacy provisions and practices? Describe the process and guidelines in place with 37 regard to the retention and destruction of PII. Cite specific records retention schedules. Yes No Records are retained and disposed of in accordance with the CDC Records Control Schedule 04-4-22 Family of HIV Surveys, Division of HIV/AIDS Prevention/Surveillance and Epidemiology, (N1-442-02-3-4, Item 1) and Division of HIV/ AIDS Prevention/Surveillance and Epidemiology, (N1-442-02-3, Item 1). Record copy of study reports are maintained in agency records from two to three years in accordance with retention schedules. Source documents for computer are disposed of when no longer needed by program officials. Personal identifiers may be deleted from records when no longer needed in the study as determined by the system manager, and as provided in the signed consent form, as appropriate. Disposal methods include erasing computer disks or tapes, burning or shredding paper materials or transferring records to the Federal Records Center when no longer needed for evaluation and analysis. Cut off closed grant, contract, or cooperative agreement files at the end of the calendar year in which the project ends or a final report is written and destroy six years after cut off. Page 6 of 8 Save Physical All printed records will be securely stored in locked file cabinets within locked offices and monitored during access. No names or other identifying information appear on data documents or in data files, as the re-contact information will be stored separately. Only designated staff will have access to the data. Describe, briefly but with specificity, how the PII will 38 be secured in the system using administrative, technical, and physical controls. Technical PII is stored in a database that provides staff with the minimum amount of data needed to perform tasks associated with their position. The application securely maintains participant information behind a firewall rendered over a Secure Sockets Layer (SSL) certificate for administrator-only access. All passwords are stored encrypted within the database, which also uses database level encryption to prevent information copying from one database to another. Web application also uses an automatic logout feature after a certain period of inactivity. Administrative All respondents will receive unique identification nonidentifiable codes, which will be stored separately from PII on a password protected computer. These codes will be used as the de-identified data set that will later be shared with CDC. CDC does not have access to the database. All staff collecting data will participate in a training that will review protections for privacy and confidentiality of all data, including PII. Only Principal Investigators may handle requests to examine data collected during this study. REVIEWER QUESTIONS: The following section contains Reviewer Questions which are not to be filled out unless the user is an OPDIV Senior Officer for Privacy. Reviewer Questions 1 Are the questions on the PIA answered correctly, accurately, and completely? Answer Yes No Reviewer Notes 2 Does the PIA appropriately communicate the purpose of PII in the system and is the purpose justified by appropriate legal authorities? Yes Do system owners demonstrate appropriate understanding of the impact of the PII in the system and provide sufficient oversight to employees and contractors? Yes No Reviewer Notes 3 No Reviewer Notes 4 Does the PIA appropriately describe the PII quality and integrity of the data? Yes No Page 7 of 8 Save Reviewer Questions Answer Reviewer Notes 5 Is this a candidate for PII minimization? Yes No Reviewer Notes 6 Does the PIA accurately identify data retention procedures and records retention schedules? Yes No Reviewer Notes 7 Are the individuals whose PII is in the system provided appropriate participation? Yes No Reviewer Notes 8 Does the PIA raise any concerns about the security of the PII? Yes No Reviewer Notes 9 Is applicability of the Privacy Act captured correctly and is a SORN published or does it need to be? Yes No Reviewer Notes 10 Is the PII appropriately limited for use internally and with third parties? Yes No Reviewer Notes 11 Does the PIA demonstrate compliance with all Web privacy requirements? Yes No Reviewer Notes 12 Were any changes made to the system because of the completion of this PIA? Yes No Reviewer Notes General Comments OPDIV Senior Official for Privacy Signature Jarell Oshodi -S Digitally signed by Jarell HHS Senior Oshodi -S Agency Official Date: 2019.03.04 for Privacy 13:38:10 -05'00' Page 8 of 8
| File Type | application/pdf |
| File Title | Att 5b_PIA |
| File Modified | 2019-03-04 |
| File Created | 2013-03-29 |