81 FR 57587 - Agency Forms Undergoing Paperwork Reduction Act Review
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention Federal Register Volume 81, Issue 163 (August 23, 2016)
Centers for Disease Control and Prevention
Federal Register Volume 81, Issue 163 (August 23, 2016)
| Page Range | 57587-57587 | |
| FR Document | 2016-20068 |
[Federal Register Volume 81, Number 163 (Tuesday, August 23, 2016)] [Notices] [Page 57587] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2016-20068] [[Page 57587]] ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day-16-16AOP] Agency Forms Undergoing Paperwork Reduction Act Review The Centers for Disease Control and Prevention (CDC) has submitted the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995. The notice for the proposed information collection is published to obtain comments from the public and affected agencies. Written comments and suggestions from the public and affected agencies concerning the proposed collection of information are encouraged. Your comments should address any of the following: (a) Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; (b) Evaluate the accuracy of the agencies estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (c) Enhance the quality, utility, and clarity of the information to be collected; (d) Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submission of responses; and (e) Assess information collection costs. To request additional information on the proposed project or to obtain a copy of the information collection plan and instruments, call (404) 639-7570 or send an email to [email protected]. Written comments and/or suggestions regarding the items contained in this notice should be directed to the Attention: CDC Desk Officer, Office of Management and Budget, Washington, DC 20503 or by fax to (202) 395-5806. Written comments should be received within 30 days of this notice. Proposed Project TRAUMATIC BRAIN INJURY (TBI) SURVEILLANCE SYSTEM--New--National Center for Injury Prevention and Control (NCIPC), Centers for Disease Control and Prevention (CDC) Background and Brief Description The Centers for Disease Control and Prevention (CDC) requests Office of Management and Budget (OMB) approval for three years for a new data collection for a Traumatic Brain Injury (TBI) Surveillance System. TBI is a significant public health concern in the United States, contributing to an estimated 2.2 million Emergency Department (ED) visits, 280,000 hospitalizations, and 50,000 deaths in 2010. These numbers, however, underestimate the true public health and economic burden of TBI in the U.S. because they are based on healthcare administrative data that only capture information on the number of ED visits, hospitalizations, and deaths identified as TBI-related. A surveillance system will accurately determine how many children and adults experience a TBI each year in the United States, and will collect information about the circumstances that identifies groups most at risk for TBI. By administering the surveillance system over time, the surveillance system can monitor trends and allow for an understanding of whether TBIs are increasing or decreasing, and whether prevention efforts are effective. Data will be collected through household survey conducted as a random digit dial telephone survey utilizing both landline and cellphones; adult respondents will be asked about their own TBI history while adult respondents with children 5-17 years of age will serve as proxies and answer questions about their children's TBI history. Information collected will produce nationally representative incidence estimates of all TBI, with a particular focus on the incidence of sports- and recreation-related TBI (SRR-TBI) among youth 5-21 years of age. Another use of the data is to produce nationally-representative estimates of TBI-related disability. Participation in the information collection is voluntary. The survey will be conducted among English or Spanish speaking participants living in the United States. The estimated annual burden hours are 4,612. There are no costs to respondents other than their time. Estimated Annualized Burden Hours ---------------------------------------------------------------------------------------------------------------- Average Number of Number of burden per Type of respondents Form name respondents responses per response (in respondent hours) ---------------------------------------------------------------------------------------------------------------- Adults 18 or older.................... Adult Eligibility 2,611 1 2/60 Screener. Adult Screener.......... 14,167 1 14/60 Adult Survey............ 2,500 1 21/60 Adolescent 12 to 17 years of age...... Adolescent Screener..... 2,058 1 5/60 Adolescent Survey....... 686 1 15/60 ---------------------------------------------------------------------------------------------------------------- Leroy A. Richardson, Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2016-20068 Filed 8-22-16; 8:45 am] BILLING CODE 4163-18-P
![Federal Register / Vol. 81, No. 163 / Tuesday, August 23, 2016 / Notices 57587
DEPARTMENT OF HEALTH AND technological collection techniques or administrative data that only capture
HUMAN SERVICES other forms of information technology, information on the number of ED visits,
e.g., permitting electronic submission of hospitalizations, and deaths identified
Centers for Disease Control and responses; and (e) Assess information as TBI-related. A surveillance system
Prevention collection costs. will accurately determine how many
To request additional information on children and adults experience a TBI
[30Day–16–16AOP]
the proposed project or to obtain a copy each year in the United States, and will
Agency Forms Undergoing Paperwork of the information collection plan and collect information about the
Reduction Act Review instruments, call (404) 639–7570 or circumstances that identifies groups
send an email to omb@cdc.gov. Written most at risk for TBI. By administering
The Centers for Disease Control and comments and/or suggestions regarding the surveillance system over time, the
Prevention (CDC) has submitted the the items contained in this notice surveillance system can monitor trends
following information collection request should be directed to the Attention: and allow for an understanding of
to the Office of Management and Budget CDC Desk Officer, Office of Management whether TBIs are increasing or
(OMB) for review and approval in and Budget, Washington, DC 20503 or decreasing, and whether prevention
accordance with the Paperwork by fax to (202) 395–5806. Written efforts are effective.
Reduction Act of 1995. The notice for comments should be received within 30
the proposed information collection is Data will be collected through
days of this notice.
published to obtain comments from the household survey conducted as a
public and affected agencies. Proposed Project random digit dial telephone survey
Written comments and suggestions utilizing both landline and cellphones;
TRAUMATIC BRAIN INJURY (TBI)
from the public and affected agencies adult respondents will be asked about
SURVEILLANCE SYSTEM—New—
concerning the proposed collection of their own TBI history while adult
National Center for Injury Prevention
information are encouraged. Your respondents with children 5–17 years of
and Control (NCIPC), Centers for
comments should address any of the age will serve as proxies and answer
Disease Control and Prevention (CDC)
following: (a) Evaluate whether the questions about their children’s TBI
proposed collection of information is Background and Brief Description history. Information collected will
necessary for the proper performance of The Centers for Disease Control and produce nationally representative
the functions of the agency, including Prevention (CDC) requests Office of incidence estimates of all TBI, with a
whether the information will have Management and Budget (OMB) particular focus on the incidence of
practical utility; (b) Evaluate the approval for three years for a new data sports- and recreation-related TBI (SRR–
accuracy of the agencies estimate of the collection for a Traumatic Brain Injury TBI) among youth 5–21 years of age.
burden of the proposed collection of (TBI) Surveillance System. TBI is a Another use of the data is to produce
information, including the validity of significant public health concern in the nationally-representative estimates of
the methodology and assumptions used; United States, contributing to an TBI-related disability. Participation in
(c) Enhance the quality, utility, and estimated 2.2 million Emergency the information collection is voluntary.
clarity of the information to be Department (ED) visits, 280,000 The survey will be conducted among
collected; (d) Minimize the burden of hospitalizations, and 50,000 deaths in English or Spanish speaking
the collection of information on those 2010. These numbers, however, participants living in the United States.
who are to respond, including through underestimate the true public health The estimated annual burden hours
the use of appropriate automated, and economic burden of TBI in the U.S. are 4,612. There are no costs to
electronic, mechanical, or other because they are based on healthcare respondents other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Average
Number of
Number of burden per
Type of respondents Form name responses per
respondents response
respondent (in hours)
Adults 18 or older ........................................... Adult Eligibility Screener ................................ 2,611 1 2/60
Adult Screener ............................................... 14,167 1 14/60
Adult Survey ................................................... 2,500 1 21/60
Adolescent 12 to 17 years of age .................. Adolescent Screener ...................................... 2,058 1 5/60
Adolescent Survey ......................................... 686 1 15/60
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
sradovich on DSK3GMQ082PROD with NOTICES
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2016–20068 Filed 8–22–16; 8:45 am]
BILLING CODE 4163–18–P
VerDate Sep<11>2014 19:42 Aug 22, 2016 Jkt 238001 PO 00000 Frm 00029 Fmt 4703 Sfmt 4703 E:\FR\FM\23AUN1.SGM 23AUN1](https://thefederalregister.org/doc/81_FR_57750/page/1.svg)
Document Created: 2018-02-09 11:40:21
Document Modified: 2018-02-09 11:40:21
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
| Publisher | Office of the Federal Register, National Archives and Records Administration | |
| Section | Notices | |
| FR Citation | 81 FR 57587 |
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