Agency Forms Undergoing Paperwork Reduction Act Review, 58393-58394 [2010-24017]

Download as PDF 58393 Federal Register / Vol. 75, No. 185 / Friday, September 24, 2010 / Notices Agency’s estimate of the burden of the proposed collection of information; (c) ways to enhance the quality, utility, and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology. Proposed Project: Ryan White HIV/ AIDS Treatment Modernization Act of 2006: Data Report Form: (OMB No. 0915–0253)—Extension The Ryan White HIV/AIDS Program Annual Data Report (or the Ryan White Data Report, formerly called the CARE Act Data Report [CADR]) was initially created in 1999 by HRSA’s HIV/AIDS Bureau. Grantees and their subcontracted service providers who are funded under Parts A, B, C, and D, and the Part F Minority AIDS Initiative of Title XXVI of the Public Health Service Act (the Ryan White HIV/AIDS Program), submit the report, which has been revised to more closely resemble the data requested in the client-level data collection instrument that these grantees and providers are now also required to submit. All parts of the Ryan White HIV/AIDS Program specify HRSA’s responsibilities in the administration of grant funds, the allocation of funds, the evaluation of programs for the population served, and the improvement of the quantity and quality of care. Because client-level data reporting requirements are relatively new for the Ryan White HIV/AIDS Program grantees, the grantees are still required to report aggregate data in the Ryan White Data Report to HRSA annually. The more mature aggregate reporting requirements provide accurate records of the providers receiving Ryan White HIV/AIDS Program funding, the services provided, and the clients served, which continue to be critical to the implementation of the legislation and necessary for HRSA to fulfill its responsibilities. The Ryan White Data Report has seven different sections containing information about the service providers; demographic information about the clients served; information about the type of core and support Number of respondents Program under which grantee is funded Part Part Part Part A B C D services provided and the number of clients served; information about counseling and testing services; clinical information about clients who received outpatient/ambulatory medical care; demographic tables for Parts C and D; and information about health insurance services. The primary purposes of the Ryan White Data Report are to: (1) Characterize the organizations where clients receive services; (2) provide information on the number and characteristics of clients who receive Ryan White HIV/AIDS Program services; and (3) enable HAB to describe the type and amount of services a client receives. In addition to meeting the goal of accountability to Congress, clients, advocacy groups, and the general public, information collected in the Ryan White Data Report is critical for HRSA, State and local grantees, and individual providers to assess the status of existing HIV-related service delivery systems. The response burden for grantees is estimated as: Responses per grantee Hours per hours Total response burden ............................................................................................................... ............................................................................................................... ............................................................................................................... ............................................................................................................... 56 59 354 98 1 1 1 1 40 40 20 20 2,240 2,360 7,080 1,960 Subtotal ..................................................................................................... 567 ........................ ........................ 13,640 Responses per provider Hours per hours The response burden for service providers is estimated as: Number of respondents Program under which provider is funded Total response burden 685 558 95 59 683 1 1 1 1 1 26 26 44 42 50 17,810 14,508 4,180 2,478 34,150 Subtotal ..................................................................................................... 2,080 ........................ ........................ 73,126 Total for Both Grantees & Providers ................................................. srobinson on DSKHWCL6B1PROD with NOTICES Part A Only ...................................................................................................... Part B Only ...................................................................................................... Part C Only ...................................................................................................... Part D Only ...................................................................................................... Funded under more than one program ........................................................... 2,647 ........................ ........................ 86,766 E-mail comments to paperwork@hrsa.gov or mail the HRSA Reports Clearance Officer, Room 10–33, Parklawn Building, 5600 Fishers Lane, Rockville, MD 20857. Written comments should be received within 60 days of this notice. Dated: September 20, 2010. Sahira Rafiullah, Director, Division of Policy and Information Coordination. [FR Doc. 2010–23929 Filed 9–23–10; 8:45 am] BILLING CODE 4165–15–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30-Day–10–0215] Agency Forms Undergoing Paperwork Reduction Act Review The Centers for Disease Control and Prevention (CDC) publishes a list of VerDate Mar<15>2010 16:12 Sep 23, 2010 Jkt 220001 PO 00000 Frm 00047 Fmt 4703 Sfmt 4703 E:\FR\FM\24SEN1.SGM 24SEN1 58394 Federal Register / Vol. 75, No. 185 / Friday, September 24, 2010 / Notices information collection requests under review by the Office of Management and Budget (OMB) in compliance with the Paperwork Reduction Act (44 U.S.C. Chapter 35). To request a copy of these requests, call the CDC Reports Clearance Officer at (404) 639–5960 or send an email to omb@cdc.gov. Send written comments to 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 Application Form and Related Forms for the Operation of the National Death Index, (OMB No. 0920–0215, Expiration 12/31/2010)—Extension—National Center for Health Statistics (NCHS), Centers for Disease Control and Prevention (CDC). Background and Brief Description Section 306 of the Public Health Service (PHS) Act (42 U.S.C.), as amended, authorizes that the Secretary of Health and Human Services (DHHS), acting through NCHS, shall collect statistics on the extent and nature of illness and disability of the population of the United States. The National Death Index (NDI) is a national data base containing identifying death record information submitted annually to NCHS by all the state vital statistics offices, beginning with deaths in 1979. Searches against the NDI file provide the states and dates of death, and the death certificate numbers of deceased study subjects. Using the NDI Plus service, researchers have the option of also receiving cause of death information for deceased subjects, thus reducing the need to request copies of death certificates from the states. The NDI Plus option currently provides the International Classification of Disease (ICD) codes for the underlying and multiple causes of death for the years 1979–2007. Health researchers must complete administrative forms in order to apply for NDI services, and submit records of study subjects for computer matching against the NDI file. A threeyear clearance is requested. There is no cost to respondents except for their time. The total estimated annual burden hours are 182. ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Number of responses per respondent Average burden per response (in hours) Type of respondents Form name Health Researchers in Government, Universities, and Private Industry. Health Researchers in Government, Universities, and Private Industry. Health Researchers in Government, Universities, and Private Industry. Application Form .................................... 50 1 2.5 Repeat Request Form ........................... 70 1 18/60 Data Transmittal Form ........................... 120 1 18/60 Dated: September 20, 2010. Maryam I. Daneshvar, Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. 2010–24017 Filed 9–23–10; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day–10–0743] srobinson on DSKHWCL6B1PROD with NOTICES Agency Forms Undergoing Paperwork Reduction Act Review The Centers for Disease Control and Prevention (CDC) publishes a list of information collection requests under review by the Office of Management and Budget (OMB) in compliance with the Paperwork Reduction Act (44 U.S.C. Chapter 35). To request a copy of these requests, call the CDC Reports Clearance Officer at (404) 639–5960 or send an email to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of Management and Budget, Washington, DC or by fax to (202) 395–5806. Written comments should be received within 30 days of this notice. VerDate Mar<15>2010 16:12 Sep 23, 2010 Jkt 220001 Proposed Project Assessment and Monitoring of Breastfeeding-Related Maternity Care Practices in Intra-partum Care Facilities in the United States and Territories (OMB Control No. 0920–0743, Exp. 10/ 31/2010)—Revision—National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC). Background and Brief Description Substantial evidence demonstrates the health benefits of breastfeeding. Breastfeeding mothers have lower risks of breast and ovarian cancers and type 2 diabetes, and breastfeeding better protects infants against infections, chronic diseases like diabetes and obesity, and even childhood leukemia and sudden infant death syndrome (SIDS). However, the groups that are at higher risk for diabetes, obesity, and poor health overall persistently have the lowest breastfeeding rates. Public health priorities for the U.S. include increasing the overall rate of breastfeeding, and reducing variation in breastfeeding rates across population subgroups. The health care system is one of the most important and effective settings to improve breastfeeding. In 2007, CDC PO 00000 Frm 00048 Fmt 4703 Sfmt 4703 conducted the first national survey of Maternity Practices in Infant Nutrition and Care (known as the mPINC Survey) in health care facilities (hospitals and free-standing childbirth centers) to provide baseline information. The survey was designed to provide baseline information and to be repeated again every two years. The second iteration of the survey was conducted in 2009. The survey inquired about patient education and support for breastfeeding throughout the maternity stay as well as staff training and maternity care policies. Each responding organization received a customized Benchmark Report as well as other feedback to use in self-assessment and quality improvement activities. CDC proposes to repeat the mPINC in 2011 using previously fielded questions and methodology. In addition to all facilities that participated in 2007 or 2009, the 2011 survey will include those that were invited but did not participate in 2007 or 2009 and any that are new since then. All birth centers and hospitals with ≥1 registered maternity bed will be screened via a brief phone call to assess their eligibility, identify additional locations, and identify the appropriate point of contact. E:\FR\FM\24SEN1.SGM 24SEN1

Agencies

[Federal Register Volume 75, Number 185 (Friday, September 24, 2010)]
[Notices]
[Pages 58393-58394]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-24017]

-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30-Day-10-0215]

Agency Forms Undergoing Paperwork Reduction Act Review

The Centers for Disease Control and Prevention (CDC) publishes a
list of

[[Page 58394]]

information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call
the CDC Reports Clearance Officer at (404) 639-5960 or send an e-mail
to omb@cdc.gov. Send written comments to 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

Application Form and Related Forms for the Operation of the
National Death Index, (OMB No. 0920-0215, Expiration 12/31/2010)--
Extension--National Center for Health Statistics (NCHS), Centers for
Disease Control and Prevention (CDC).

Background and Brief Description

Section 306 of the Public Health Service (PHS) Act (42 U.S.C.), as
amended, authorizes that the Secretary of Health and Human Services
(DHHS), acting through NCHS, shall collect statistics on the extent and
nature of illness and disability of the population of the United
States.
The National Death Index (NDI) is a national data base containing
identifying death record information submitted annually to NCHS by all
the state vital statistics offices, beginning with deaths in 1979.
Searches against the NDI file provide the states and dates of death,
and the death certificate numbers of deceased study subjects.
Using the NDI Plus service, researchers have the option of also
receiving cause of death information for deceased subjects, thus
reducing the need to request copies of death certificates from the
states. The NDI Plus option currently provides the International
Classification of Disease (ICD) codes for the underlying and multiple
causes of death for the years 1979-2007. Health researchers must
complete administrative forms in order to apply for NDI services, and
submit records of study subjects for computer matching against the NDI
file. A three-year clearance is requested. There is no cost to
respondents except for their time. The total estimated annual burden
hours are 182.

Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Health Researchers in Government, Application Form......... 50 1 2.5
Universities, and Private Industry.
Health Researchers in Government, Repeat Request Form...... 70 1 18/60
Universities, and Private Industry.
Health Researchers in Government, Data Transmittal Form.... 120 1 18/60
Universities, and Private Industry.
----------------------------------------------------------------------------------------------------------------

Dated: September 20, 2010.
Maryam I. Daneshvar,
Reports Clearance Officer, Centers for Disease Control and Prevention.
[FR Doc. 2010-24017 Filed 9-23-10; 8:45 am]
BILLING CODE 4163-18-P

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