Agency Forms Undergoing Paperwork Reduction Act Review, 21810-21811 [E9-10938]
Download as PDF
21810
Federal Register / Vol. 74, No. 89 / Monday, May 11, 2009 / Notices
Revision—National Center on Birth
Defects and Developmental Disabilities
(NCBDDD), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The National Center on Birth Defects
and Developmental Disabilities at CDC
promotes the health of babies, children,
and adults with disabilities. As part of
these efforts the Center is actively
involved in addressing hearing loss (HL)
among newborns and infants. HL is a
common birth defect that affects
approximately 12,000 infants each year
and, when left undetected, can result in
developmental delays. As awareness
about infant HL increases, so does the
demand for accurate information about
rates of screening, referral, loss to
follow-up, and incidence. This
information is important for helping to
ensure infants and children are
territories. The request to complete this
survey is planned to be disseminated to
respondents via an e-mail, which will
include a summary of the request and
other relevant information. Minor
changes to this survey, based on
respondent feedback, are planned in
order to make the survey easier to
complete and further improve data
quality. These changes include splitting
the previously combined questions
about the number of infants that died
and parents refused into two separate
questions, adding a question about how
many infants with hearing loss are
receiving only monitoring services,
simplifying the table for reporting type
and severity of hearing loss data, and
expanding the maternal race categories
in the demographic section.
There are no costs to the respondents
other than their time.
receiving recommended screening and
follow-up services, documenting the
occurrence and etiology of differing
degrees of HL among infants, and
determining the overall impact of infant
HL on future outcomes, such as
cognitive development, and family
dynamics. These data will also assist
state Early Hearing Detection and
Intervention (EHDI) programs with
quality improvement activities and
provide information that will be helpful
in assessing the impact of federal
initiatives. The public will be able to
access this information via the CDC
EHDI Web site (https://www.cdc.gov/
ncbddd/ehdi/data.htm).
Given the lack of a standardized and
readily accessible source of data, the
CDC EHDI program developed a survey
to be used annually that utilizes
uniform definitions to collect aggregate,
standardized EHDI data from states and
ESTIMATED ANNUALIZED BURDEN HOURS
Respondents
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
(in hours)
State and territory EHDI Program Coordinators ..............................................
53
1
4
212
Dated: May 5, 2009.
Marilyn S. Radke,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. E9–10937 Filed 5–8–09; 8:45 am]
BILLING CODE 4163–18–P
Centers for Disease Control and
Prevention
[30Day–09–08BL]
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) 395–6974. Written
comments should be received within 30
days of this notice.
15:05 May 08, 2009
Jkt 217001
Multi-site HIV Testing in Community
Mental Health Settings Serving African
Americans—New—National Center for
HIV, Viral Hepatitis, STD and TB
Prevention (NCHHSTP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
VerDate Nov<24>2008
Proposed Project
People with severe mental illness,
including those with substance use
disorders, are at increased risk of
infection with human
immunodeficiency virus (HIV) when
compared with the general population.
However, not enough is known about
the risk behaviors, willingness to be
tested for HIV, and prevalence of HIV
among persons with severe mental
illness. In addition, the interrelations
among diagnosis of HIV, compliance
with medical care, subsequent risk
behaviors, and the course of mental
illness have not been well-described.
Mental health clinics are an important
setting for testing and promoting
prevention efforts against the
transmission of HIV.
The objectives of this project are to (1)
demonstrate improved access to HIV
testing and linkage to care in
participating mental health care settings
and (2) describe the relationship
between mental illness, HIV risk
behaviors, and access to testing and
PO 00000
Frm 00036
Fmt 4703
Sfmt 4703
services, in order to inform the
development of optimal prevention
interventions for persons with severe
mental illness. Staff at selected
implementation sites will offer testing
for HIV to clients and administer a brief
survey to assess risk behaviors, previous
access to similar testing services, and
mental health symptoms. This project
will collect data from clients using brief
surveys administered on a voluntary
basis. Collection of data will provide
information on client demographics;
current behaviors that may facilitate
HIV transmission, including sexual and
drug-use behaviors; current psychiatric
symptoms, determined using brief rating
scales; access and barriers to HIV
testing, prevention, and treatment
services; and adherence to psychiatric
and medical treatment regimens. CDC is
requesting approval for a 2-year
clearance for data collection. Data will
be collected in 6 sites which provide
mental health services.
The goal will be to approach 716
persons annually for participation in the
study and interview a total of 600
persons. Based on the University of
Pennsylvania’s prior experience
working in mental health settings, it is
estimated that of the 716 approached for
participation in the study, the response
rate will be approximately 90%. Of the
644 persons approached who agree to be
E:\FR\FM\11MYN1.SGM
11MYN1
21811
Federal Register / Vol. 74, No. 89 / Monday, May 11, 2009 / Notices
surveyed, it is estimated that 95% of
persons will meet the eligibility criteria
and 98% will be able to provide
informed consent, as determined by the
consent comprehension test. Therefore,
the goal will be to interview a sample
of 600 persons annually for two years;
300 in each of the two project areas of
Baltimore and Philadelphia. The
structured interview will take
approximately 20 minutes to complete.
Participation is voluntary. Data
collection will provide important
insights into the relationship between
psychiatric illness and risk behaviors for
HIV.
There is no cost to the respondents
other than their time. The total
annualized burden hours are 313.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Form name
Approached individual .....................................
Eligible participant ...........................................
Consented participant .....................................
Eligibility Screener ..........................................
Consent Questionnaire ..................................
Core Questionnaire ........................................
Dated: May 5, 2009.
Marilyn S. Radke,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E9–10938 Filed 5–8–09; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of
Meeting
Pursuant to section 10(a) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of a meeting of the
National Institutes of Health Peer
Review Advisory Committee.
The meeting will be open to the
public, with attendance limited to space
available. Individuals who plan to
attend and need special assistance, such
as sign language interpretation or other
reasonable accommodations, should
notify the Contact Person listed below
in advance of the meeting.
Name of Committee: National Institutes of
Health Peer Review Advisory Committee.
Date: June 8, 2009.
Time: 8:30 a.m. to 5 p.m.
Agenda: Provide technical and scientific
advice and recommendations to the NIH
Director, the Deputy Director for Extramural
Research, and the Director of the Center for
Scientific Review (CSR) on all procedures
and policies related to the process of peer
review by which the scientific and technical
merit of NIH grant applications is assessed.
Place: Hilton Washington/Rockville, 1750
Rockville Pike, Rockville, MD 20852.
Contact Person: Cheryl A. Kitt, PhD, Center
for Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3030,
MSC 7776, Bethesda, MD 20892, 301–435–
1112, kittc@csr.nih.gov.
Any interested person may file written
comments with the committee by forwarding
the statement to the Contact Person listed on
VerDate Nov<24>2008
15:05 May 08, 2009
Jkt 217001
this notice. The statement should include the
name, address, telephone number and when
applicable, the business or professional
affiliation of the interested person.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.306, Comparative Medicine;
93.333, Clinical Research, 93.306, 93.333,
93.337, 93.393–93.396, 93.837–93.844,
93.846–93.878, 93.892, 93.893, National
Institutes of Health, HHS)
Dated: May 04, 2009.
Jennifer Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. E9–10781 Filed 5–8–09; 8:45 am]
BILLING CODE 4140–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute on Alcohol Abuse
and Alcoholism; Notice of Closed
Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute on
Alcohol Abuse and Alcoholism Special
Emphasis Panel; RFA–AA–09–006—
Mechanism of Alcohol-Induced Organ
Damage (R01).
Date: July 13–14, 2009.
Time: 8 a.m. to 5 p.m.
PO 00000
Frm 00037
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
644
612
600
Average
burden per
response
(in hours)
1
1
1
1/60
10/60
20/60
Agenda: To review and evaluate grant
applications.
Place: Hyatt Regency Bethesda, One
Bethesda Metro Center, 7400 Wisconsin
Avenue, Bethesda, MD 20814.
Contact Person: Philippe Marmillot, PhD,
National Institutes of Health, National
Institute on Alcohol Abuse and Alcoholism,
5635 Fishers Lane, Rm 2017, Bethesda, MD
20892, 301–443–2861,
marmillotp@mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.271, Alcohol Research
Career Development Awards for Scientists
and Clinicians; 93.272, Alcohol National
Research Service Awards for Research
Training; 93.891, Alcohol Research Center
Grants, National Institutes of Health, HHS)
Dated: May 4, 2009.
Jennifer Spaeth,
Director, Office of Federal Advisory
Committee Policy.
[FR Doc. E9–10786 Filed 5–8–09; 8:45 am]
BILLING CODE 4140–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of
Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
E:\FR\FM\11MYN1.SGM
11MYN1
Agencies
[Federal Register Volume 74, Number 89 (Monday, May 11, 2009)]
[Notices]
[Pages 21810-21811]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-10938]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-09-08BL]
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 e-mail
to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC or by fax to (202) 395-6974.
Written comments should be received within 30 days of this notice.
Proposed Project
Multi-site HIV Testing in Community Mental Health Settings Serving
African Americans--New--National Center for HIV, Viral Hepatitis, STD
and TB Prevention (NCHHSTP), Centers for Disease Control and Prevention
(CDC).
Background and Brief Description
People with severe mental illness, including those with substance
use disorders, are at increased risk of infection with human
immunodeficiency virus (HIV) when compared with the general population.
However, not enough is known about the risk behaviors, willingness to
be tested for HIV, and prevalence of HIV among persons with severe
mental illness. In addition, the interrelations among diagnosis of HIV,
compliance with medical care, subsequent risk behaviors, and the course
of mental illness have not been well-described. Mental health clinics
are an important setting for testing and promoting prevention efforts
against the transmission of HIV.
The objectives of this project are to (1) demonstrate improved
access to HIV testing and linkage to care in participating mental
health care settings and (2) describe the relationship between mental
illness, HIV risk behaviors, and access to testing and services, in
order to inform the development of optimal prevention interventions for
persons with severe mental illness. Staff at selected implementation
sites will offer testing for HIV to clients and administer a brief
survey to assess risk behaviors, previous access to similar testing
services, and mental health symptoms. This project will collect data
from clients using brief surveys administered on a voluntary basis.
Collection of data will provide information on client demographics;
current behaviors that may facilitate HIV transmission, including
sexual and drug-use behaviors; current psychiatric symptoms, determined
using brief rating scales; access and barriers to HIV testing,
prevention, and treatment services; and adherence to psychiatric and
medical treatment regimens. CDC is requesting approval for a 2-year
clearance for data collection. Data will be collected in 6 sites which
provide mental health services.
The goal will be to approach 716 persons annually for participation
in the study and interview a total of 600 persons. Based on the
University of Pennsylvania's prior experience working in mental health
settings, it is estimated that of the 716 approached for participation
in the study, the response rate will be approximately 90%. Of the 644
persons approached who agree to be
[[Page 21811]]
surveyed, it is estimated that 95% of persons will meet the eligibility
criteria and 98% will be able to provide informed consent, as
determined by the consent comprehension test. Therefore, the goal will
be to interview a sample of 600 persons annually for two years; 300 in
each of the two project areas of Baltimore and Philadelphia. The
structured interview will take approximately 20 minutes to complete.
Participation is voluntary. Data collection will provide important
insights into the relationship between psychiatric illness and risk
behaviors for HIV.
There is no cost to the respondents other than their time. The
total annualized burden hours are 313.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Type of respondent Form name respondents responses per response (in
respondent hours)
----------------------------------------------------------------------------------------------------------------
Approached individual................. Eligibility Screener.... 644 1 1/60
Eligible participant.................. Consent Questionnaire... 612 1 10/60
Consented participant................. Core Questionnaire...... 600 1 20/60
----------------------------------------------------------------------------------------------------------------
Dated: May 5, 2009.
Marilyn S. Radke,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E9-10938 Filed 5-8-09; 8:45 am]
BILLING CODE 4163-18-P