The Performance Measures Project: Improving Performance Measurement and Monitoring By CDC Programs
Part A: Justification
July 22, 2019
Contact: J. Stan Lehman
Telephone: (404) 639-2041
E-mail: syl5@cdc.gov
Program Performance and Evaluation Office
Office of the Associate Director for Policy and Strategy
Office of the Director
Centers for Disease Prevention and Control
Atlanta, Georgia
TABLE OF CONTENTS
A. Justification
Circumstances Making the Collection of Information Necessary
Purposes and Use of Information Collection
Use of Improved Information Technology and Burden Reduction
Efforts to Identify Duplication and Use of Similar Information
Impact on Small Businesses or Other Small Entities
Consequences of Collecting the Information Less Frequently
Special Circumstances Relating to the Guidelines of 5 CFR 1320.5
Comments in Response to the Federal Register Notice and Efforts to Consult Outside the Agency
Explanation of Any payment or Gift to Respondents
Protection of the Privacy and Confidentiality of Information Provided by Respondents
Institutional Review Board (IRB) and Justification for Sensitive Questions
Estimates of Annualized Burden Hours and Costs
Estimates of Other Total Annual Cost Burden to Respondents or Record Keepers
Estimates of Annualized Cost to the Federal Government
Explanation for Program Changes or Adjustments
Plans for Tabulation and Publication and Project Time Schedule
Reason(s) Display of OMB Expiration Date is Inappropriate
Exceptions to Certification for Paperwork Reduction Act Submissions
List of Attachments
Authorizing Legislation
Sample Performance Measure Technical Specification Instrument
Sample Performance Measure Reporting Instrument
60 Day Federal Register Notice
Federal Register Notice Comments
Research Determination (1 of 2)
Research Determination (2 of 2)
PPEO GenIC request template
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1. Circumstances Making the Collection of Information Necessary
Each year, approximately 75% of the CDC’s congressionally appropriated funding goes to extramural organizations, including state and local partners, via contracts, grants, and, most commonly, cooperative agreements. A cooperative agreement is an award mechanism used when there will be substantial Federal programmatic involvement, meaning that the CDC program staff will collaborate or participate in project or program activities. The availability of funding for cooperative agreements is announced through a Notice of Funding Opportunity (NOFO). CDC awards approximately 65 new domestic, non-research NOFOs each year (each funded for 1 to 5 years). Cooperative agreements may have only a few funded recipients or more than 50 (such as when a CDC program provides funding to all states and territories). For the purposes of this generic, CDC programs developing new high profile, domestic, non-research NOFOs are eligible to participate. High profile NOFOs, as defined for this project, include those that fund all 50 states, have budgets higher than $10 million per year, and/or have significant stakeholder (partners, Congress, etc.) interest.
Monitoring and reporting of program performance is required of any non-federal entity receiving federal funds under 45 CFR 75.342 (Attachment 1); “The non-Federal entity must monitor its activities under Federal awards to assure compliance with applicable Federal requirements and performance expectations are being achieved”. Under this requested approval, CDC programs may customize the sample “Performance Measure Technical Specification Instrument ” (Attachment 2) and the sample “Performance Measure Reporting Instrument” (Attachment 3) to measure, at the local level, the desired public health outcomes of a particular cooperative agreement, in compliance with the Paperwork Reduction Act (PRA). Individual collection requests submitted under this generic approval will include the tailored forms and a supplementary template (Attachment 8).
The sample Performance Measure Technical Specification Instrument provides standardized technical specifications for operationalizing performance measures. The CDC program, in collaboration with the funded recipients will document these technical specifications for each performance measure developed for a particular cooperative agreement. The sample Performance Measure Reporting Instrument is what the CDC programs will adapt and use for all recipients to report the performance data in a standardized way.
This is the initial request for a generic clearance, thus CDC has no information from use by any CDC program offices. However, this request is based on the recent approval of a similar generic clearance (OMB approval number: 0970-0490, expiration date 1/31/2020) for the Administration for Children and Families (ACF).
The program-specific, generic ICs will be uncontroversial, low burden, and provide a significant benefit to recipients. The data collection is requested for three years.
2. Purpose and Use of the Information Collection
Information collection instruments that are customized to reflect program-specific performance measures will allow CDC programs to collect data for a particular cooperative agreement in a uniform and systematic manner across all recipients, will provide a single reporting format, and will reduce the burden on individual funded recipients. Standardized collection and reporting of performance measures will result in higher quality performance data and allow CDC to monitor how individual recipients are progressing toward implementing the activities and achieving their outcomes and allow CDC to more easily aggregate data across all funded organizations. These data will be used by CDC to monitor trends for each performance measure over the life of the cooperative agreement and show a program’s successes and challenges, make course corrections as needed, and identify technical assistance needs.
This generic clearance will also allow the funded recipients to efficiently report their performance data using an instrument customized to a particular cooperative agreement. Having a standardized instrument will make it easier for them to report data consistently and accurately across reporting periods. The staff from funded recipient organizations will be able to more easily enter data and review for completeness, enter basic summary data for reports, and save required data for use with other reporting systems.
3. Use of Improved Information Technology and Burden Reduction
CDC Programs and funded recipients will use some form of electronic data collection. Building on existing data infrastructure, this will be either a web page, email, or preferably, On-line Data Collection System (OLDC). OLDC is the most sophisticated approach based on web technology. Recipients may enter and retrieve information pertinent to their local program activity through electronic forms closely resembling the paper forms. OLDC reduces paperwork, allows for quicker processing, automatically completes required calculations, checks for potential errors, and provides security.
4. Efforts to Identify Duplication and Use of Similar Information
The information collected from funded recipients is not available from other sources in a consistent format.
5. Impact on Small Businesses or Other Small Entities
No small businesses will be involved in this data collection, unless contracted by local funding recipients.
6. Consequences of Collecting the Information Less Frequently
Performance measure data will be collected at least annually in accordance with program guidance and relevant cooperative agreement award terms and conditions. Less frequent reporting would undermine accountability efforts at all levels and negatively impact monitoring recipient progress. The periodic reporting schedule ensures that CDC responses to inquiries from HHS, Congress and other stakeholders are based on timely and up-to-date information.
7. Special Circumstances Relating to the Guidelines of 5 CFR 1320.5
This request fully complies with the regulation 5 CFR 1320.5.
8. Comments in Response to the Federal Register Notice and Efforts to Consult Outside the Agency
A 60 Day Federal Register Notice (60-Day-19-19IJ; Docket No. CDC-2018-0118) was published in the Federal Register on 2/7/2019; volume 84, page 2521 (Attachment 4).
CDC received one non-substantive comment to the 60 day FRN (Attachment 5). No response was given.
CDC consulted with Molly Jones of ACF PRA leads Mary.Jones@acf.hhs.gov) in development of this request.
9. Explanation of Any Payment or Gift to Respondents
Respondents will not receive payments or gifts for providing information.
10. Protection of the Privacy and Confidentiality of Information Provided by Respondents
Staff from the CDC Office of Science have reviewed this Information Collection Request and have determined that the Privacy Act is not applicable (Attachment 6, Attachment 7). The data collection does not involve collection of sensitive or identifiable personal information. Although contact information is obtained for each funded recipient (state or local jurisdiction), the contact person provides information about the organization, not personal information. No system of records will be created under the Privacy Act.
Recipients are required to provide data as a condition of cooperative agreement funding and will submit data via secure mechanism (eg, email, password protected website, Sharepoint).
While consent is not required to report aggregate data, recipient consent will be obtained if their specific data are used for publications, reports or other publicly disseminated information.
Aggregated information will be stored on an internal CDC SQL server subject to CDC’s information security guidelines. CDC staff, technical assistance, and training contractors will have varying levels of access to the system with role-appropriate security training, based on the requirements of their position(s).
11. Institutional Review Board (IRB) and Justification for Sensitive Questions
The proposed generic clearance does not collect sensitive information.
12. Estimates of Annualized Burden Hours and Costs
A. Estimated Annualized Burden Hours
Up to 25 CDC cooperative agreements will be included in this project; phased in over the three year project period. There will be approximately 35 awards per participating cooperative agreement for a maximum of 875 recipients (across all participating cooperative agreements).
Table A.12-A. Estimated Annualized Burden to Respondents
Type of Respondents |
Form Name |
Number of respondents |
Number of responses per respondent per year |
Average burden per response (in hours) |
Total burden (in hours) |
CDC Cooperative Agreement Funding Recipients |
Performance Measures Project Information Collection Tool |
875 |
1 |
40 |
35,000 |
Total |
|
|
|
|
35,000 |
B. Estimated Annualized Cost to Respondents
Estimates for the average hourly wage for respondents are based on the U.S. Department of Labor Bureau (DOL) of Labor Statistics May 2014 National Occupational Employment and Wage Estimates (http://www.bls.gov/oes/current/oes_nat.htm). Based on DOL data, the average hourly wage for an epidemiologist is estimated to be $37.37. The total estimated annualized cost is summarized in Table A.12-B.
Table A.12-B. Estimated Annualized Cost to Respondents
Type of Respondents |
Total burden (in Hours) |
Average Hourly Wage |
Total Cost |
CDC Award Recipients |
35,000 |
$37.37 |
$1,307,950 |
13. Estimates of Other Total Annual Cost Burden to Respondents or Record
Keepers
No capital or maintenance costs are expected.
14. Estimates of Annualized Cost to the Federal Government
The cost to the Federal Government is approximately $43,800; 20% of a GS-14 step 5 epidemiologist and 25% of a GS-12 step 1 public health analyst).
15. Explanation for Program Changes or Adjustments
This is a new generic clearance.
16. Plans for Tabulation and Publication and Project Time Schedule
A. Time schedule for the entire project
OMB approval is requested for three years. CDC programs will begin participating by the end of 2019. Each CDC program developing a new cooperative agreement will submit a generic information collection for use by all funded recipients. Reports will be generated by the recipients per the cooperative agreement requirements. Data collection will begin when funding is awarded and will continue throughout the funding cycle.
B. Publication plan
Information collected by the funded organizations will be reported in internal CDC documents and shared with recipients. Summary data will be provided for inquiries from HHS, Congress and/or other stakeholders. Individual programs that are planning other types of publications will include that information in their specific request.
C. Analysis plan
CDC will not use complex statistical methods for analyzing information. All information will be aggregated for each cooperative agreement and reported with no personal identifying information in external documents. The information collected is meant primarily for program improvement and accountability; it is not intended to be used as the principal basis for policy decisions.
Most statistical analyses will be descriptive and will vary by individual cooperative agreement need.
17. Reason(s) Display of OMB Expiration Date is Inappropriate
The Sample Performance Measure Instruments (Attachment 2, Attachment 3) will display the expiration date for OMB approval. All collections under this generic will also include the OMB expiration date.
18. Exceptions to Certification for Paperwork Reduction Act Submissions
There are no exceptions to the certification statement.
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