Agency for Toxic Substances and Disease Registry; Agency Forms Undergoing Paperwork Reduction Act Review, 6801-6802 [2012-2971]
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6801
Federal Register / Vol. 77, No. 27 / Thursday, February 9, 2012 / Notices
Atlanta, GA 30333, telephone 770–488–
3313.
Dated: February 3, 2012.
Ken Rose,
Director, Office of Policy, Planning and
Evaluation, National Center for
Environmental Health/Agency for Toxic
Substances and Disease Registry.
[FR Doc. 2012–2955 Filed 2–8–12; 8:45 am]
BILLING CODE 4163–70–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–12–09BK]
Agency for Toxic Substances and
Disease Registry; Agency Forms
Undergoing Paperwork Reduction Act
Review
The Agency for Toxic Substances and
Disease Registry (ATSDR) 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/ATSDR Reports Clearance
Officer at (404) 639–7570 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
Registration of Individuals Displaced
by the Hurricanes Katrina and Rita
(Pilot Project)—New—Agency for Toxic
Substances and Disease Registry
(ATSDR), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
On August 29, 2005, Hurricane
Katrina made landfall on the coast of the
Gulf of Mexico near New Orleans,
Louisiana, and became one of the most
deadly and destructive storms in U.S.
history. Also occurring in 2005,
Hurricane Rita was the fourth-most
intense Atlantic hurricane ever recorded
and the most intense tropical cyclone
ever observed in the Gulf of Mexico.
Following the initial phase of the
response, the Federal Emergency
Management Agency (FEMA) assumed
the primary role for housing displaced
persons over the intermediate term. To
support those needing temporary
housing, FEMA provided over 130,000
travel trailers, park homes, and mobile
homes for persons displaced by the
above mentioned storms. However,
some persons living in trailers
complained of an odor or of eye or
respiratory tract irritation.
FEMA entered into an Interagency
Agreement with the Centers for Disease
Control and Prevention (CDC)/ATSDR
on August 16, 2007 to conduct a
comprehensive public health
assessment, based on objective and
credible research, of air quality
conditions present in FEMA housing
units to guide FEMA policy makers and
inform the public as to the actual
conditions in the field and any actions
required to better promote a safe and
healthful environment for the disaster
victims FEMA housed in the units.
FEMA’s agreement with the CDC
includes an initial formaldehyde
exposure assessment as well as a
subsequent long-term study of the
health effects among resident children.
Formaldehyde testing conducted and
evaluated by the CDC pursuant to the
initial exposure assessment has
identified the need to evaluate the
feasibility of establishing a national
registry to identify and monitor the
health of disaster victims who occupied
FEMA-provided temporary housing
units. The establishment of such a
registry would complement the longterm health effects study set forth in the
FEMA–CDC Interagency Agreement.
The proposed pilot registry will have
two goals: Primary Goal: Test the
feasibility and cost of contacting and
enrolling members in a registry by
collecting and verifying phone
interview data. Secondary Goal: Test the
difference in prevalence rates of health
conditions compared to national
surveys (i.e., NHANES and NHIS).
The data collected in the pilot registry
and the evaluation of the pilot registry
will be used to determine the feasibility
and estimate the costs of developing and
populating a more complete registry of
people affected by Hurricanes Katrina
and Rita. In addition, comparisons of
prevalence rates of health outcomes
obtained through the pilot registry with
estimates from national surveys will
help determine the utility of conducting
a full registry. For example, if all or
most health outcomes do not appear to
be in excess, the value of a full registry
may be questionable.
A pre-registration datasets will be
created before enrollment. This dataset
will be populated with contact
information of the occupants of
temporary housing units provided by
FEMA. FEMA provided the datasets for
this pilot registry.
A computer-assisted telephone
interview (CATI) system based on a
paper questionnaire will be used during
all interviews to collect data for this
project. The first part will consist of
screening questions to determine
eligibility for enrollment. The second
part will contain contact information of
the registrant and other household
members, demographics, and health
status questions, focusing on respiratory
outcomes and mental health.
The two minute screening
questionnaire will be administered to a
total of 8,000 respondents. Annualized
over a two year period, 4,000 will be
screened. The 25 minute main
questionnaire will be administered to a
total of 5,000 respondents. Annualized
over a two year period, 2,500 occupants
will complete the main questionnaire.
There are no costs to the respondents
other than their time. The total
estimated annual burden hours are
1,176.
ESTIMATED ANNUALIZED BURDEN HOURS
mstockstill on DSK4VPTVN1PROD with NOTICES
Form
Temporary and Non-Temporary housing unit
occupants.
Main questionnaire ..........................................
Screening .......................................................
questionnaire ..................................................
2,500 ..............................................................
VerDate Mar<15>2010
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Jkt 226001
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Frm 00030
Fmt 4703
Number of
responses per
respondent
Number of
respondents
Respondents
Sfmt 4703
E:\FR\FM\09FEN1.SGM
4,000
1
1
25/60
09FEN1
Average
burden per
response
(in hours)
2/60
6802
Federal Register / Vol. 77, No. 27 / Thursday, February 9, 2012 / Notices
Kimberly Lane,
Reports Clearance Officer, Agency for Toxic
Substances and Disease Registry.
[FR Doc. 2012–2971 Filed 2–8–12; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–12–12AG]
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) 639–7570 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
HIV Prevention among Latino MSM:
Evaluation of a locally developed
intervention—New—National Center for
HIV/AIDS, Viral Hepatitis, STD, TB
Prevention (NCHHSTP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Latinos are the largest and fastest
growing ethnic minority group in the
U.S. and have the second highest rate of
HIV/AIDS diagnoses of all racial/ethnic
groups in the country. From the
beginning of the epidemic through 2007,
Latinos accounted for 17% of all AIDS
cases reported to the CDC. Among
Latino males, male-to-male sexual
contact is the single most important
source of HIV infection, accounting for
46% of HIV infections in U.S.-born
Latino men from 2001 to 2005, and for
more than one-half of HIV infections
among South American, Cuban, and
Mexican-born Latino men in the U.S.
(CDC, 2007a; 2007b). In 2006, male-tomale sex accounted for 72% of new HIV
infections among Latino males. Relative
to other men who have sex with men
(MSM), the rate of HIV infection among
Latino MSM is twice the rate recorded
among whites (43.1 vs. 19.6 per
100,000).
Despite the high levels of infection
risk that affect Latino MSM, no
efficacious interventions to prevent
infection by HIV and other sexually
transmitted diseases (STDs) are
available for this vulnerable population.
CDC’s Prevention Research Synthesis
group, whose role is to identify HIV
prevention interventions that have met
rigorous criteria for demonstrating
evidence of efficacy, has not identified
any behavioral interventions for Latino
MSM that meet current efficacy criteria,
and no such interventions are listed in
CDC’s 2011 update of its Compendium
of Evidence-Based HIV Behavioral
Interventions (https://www.cdc.gov/hiv/
topics/research/prs/compendiumevidence-based-interventions.htm).
There is an urgent need for efficacious,
culturally congruent HIV/STD
prevention interventions for Latino
MSM.
The purpose of this project is to test
the efficacy of an HIV prevention
intervention for reducing sexual risk
among Latino men who have sex with
men in North Carolina. The HOLA en
Grupos intervention is a Spanishlanguage, small-group, 4-session
intervention that is designed to increase
consistent and correct condom use and
HIV testing among Latino MSM and to
affect other behavioral and psychosocial
factors that can increase their
vulnerability of HIV/STD infection. This
study will use a randomized controlled
trial design to assess the efficacy of the
HOLA en Grupos intervention
compared to a general health
comparison intervention.
CDC is requesting approval for a
3-year clearance for data collection. The
data collection system involves
screening of potential study participants
for eligibility, collection of participants’
contact information, and measures of
intervention and comparison
participants’ socio-demographic
characteristics, health seeking actions,
HIV/STD and substance use-related risk
behaviors, and psychosocial factors at
baseline before intervention delivery
and 6 months after intervention
delivery. An estimated 350 men will be
screened for eligibility in order to enroll
the 300 men required for the study. The
baseline and the 6-month follow-up
assessments will be similar. However,
the 6-month assessment will ask study
participants fewer questions because
there is no need to ask all questions
during both assessments. Collection of
eligibility information from potential
participants will require about
10 minutes; collection of baseline
assessment information will require
about 1 hour and 45 minutes; and
collection of the 6-month follow-up
assessment information will require
about 1 hour.
The total estimated annual burden
hours are 883. There is no cost to
participants other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
Prospective Study Participant .........................
Enrolled Study Participant ..............................
Enrolled Study Participant ..............................
mstockstill on DSK4VPTVN1PROD with NOTICES
Type of respondent
Participant Screening Form ...........................
Baseline Assessment .....................................
6-month follow-up assessment ......................
350
300
300
Kimberly S. Lane,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. 2012–2969 Filed 2–8–12; 8:45 am]
BILLING CODE 4163–18–P
VerDate Mar<15>2010
19:21 Feb 08, 2012
Jkt 226001
PO 00000
Frm 00031
Fmt 4703
Sfmt 4703
E:\FR\FM\09FEN1.SGM
09FEN1
Number
responses per
respondent
1
1
1
Average
burden per
respondent
(in hours)
10/60
1.75
1
Agencies
[Federal Register Volume 77, Number 27 (Thursday, February 9, 2012)]
[Notices]
[Pages 6801-6802]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-2971]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-12-09BK]
Agency for Toxic Substances and Disease Registry; Agency Forms
Undergoing Paperwork Reduction Act Review
The Agency for Toxic Substances and Disease Registry (ATSDR)
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/ATSDR Reports Clearance Officer at (404) 639-
7570 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
Registration of Individuals Displaced by the Hurricanes Katrina and
Rita (Pilot Project)--New--Agency for Toxic Substances and Disease
Registry (ATSDR), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
On August 29, 2005, Hurricane Katrina made landfall on the coast of
the Gulf of Mexico near New Orleans, Louisiana, and became one of the
most deadly and destructive storms in U.S. history. Also occurring in
2005, Hurricane Rita was the fourth-most intense Atlantic hurricane
ever recorded and the most intense tropical cyclone ever observed in
the Gulf of Mexico. Following the initial phase of the response, the
Federal Emergency Management Agency (FEMA) assumed the primary role for
housing displaced persons over the intermediate term. To support those
needing temporary housing, FEMA provided over 130,000 travel trailers,
park homes, and mobile homes for persons displaced by the above
mentioned storms. However, some persons living in trailers complained
of an odor or of eye or respiratory tract irritation.
FEMA entered into an Interagency Agreement with the Centers for
Disease Control and Prevention (CDC)/ATSDR on August 16, 2007 to
conduct a comprehensive public health assessment, based on objective
and credible research, of air quality conditions present in FEMA
housing units to guide FEMA policy makers and inform the public as to
the actual conditions in the field and any actions required to better
promote a safe and healthful environment for the disaster victims FEMA
housed in the units. FEMA's agreement with the CDC includes an initial
formaldehyde exposure assessment as well as a subsequent long-term
study of the health effects among resident children. Formaldehyde
testing conducted and evaluated by the CDC pursuant to the initial
exposure assessment has identified the need to evaluate the feasibility
of establishing a national registry to identify and monitor the health
of disaster victims who occupied FEMA-provided temporary housing units.
The establishment of such a registry would complement the long-term
health effects study set forth in the FEMA-CDC Interagency Agreement.
The proposed pilot registry will have two goals: Primary Goal: Test
the feasibility and cost of contacting and enrolling members in a
registry by collecting and verifying phone interview data. Secondary
Goal: Test the difference in prevalence rates of health conditions
compared to national surveys (i.e., NHANES and NHIS).
The data collected in the pilot registry and the evaluation of the
pilot registry will be used to determine the feasibility and estimate
the costs of developing and populating a more complete registry of
people affected by Hurricanes Katrina and Rita. In addition,
comparisons of prevalence rates of health outcomes obtained through the
pilot registry with estimates from national surveys will help determine
the utility of conducting a full registry. For example, if all or most
health outcomes do not appear to be in excess, the value of a full
registry may be questionable.
A pre-registration datasets will be created before enrollment. This
dataset will be populated with contact information of the occupants of
temporary housing units provided by FEMA. FEMA provided the datasets
for this pilot registry.
A computer-assisted telephone interview (CATI) system based on a
paper questionnaire will be used during all interviews to collect data
for this project. The first part will consist of screening questions to
determine eligibility for enrollment. The second part will contain
contact information of the registrant and other household members,
demographics, and health status questions, focusing on respiratory
outcomes and mental health.
The two minute screening questionnaire will be administered to a
total of 8,000 respondents. Annualized over a two year period, 4,000
will be screened. The 25 minute main questionnaire will be administered
to a total of 5,000 respondents. Annualized over a two year period,
2,500 occupants will complete the main questionnaire.
There are no costs to the respondents other than their time. The
total estimated annual burden hours are 1,176.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Respondents Form Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Temporary and Non-Temporary housing Screening............... 4,000 1 2/60
unit occupants. questionnaire...........
Main questionnaire.................... 2,500................... 1 25/60
----------------------------------------------------------------------------------------------------------------
[[Page 6802]]
Kimberly Lane,
Reports Clearance Officer, Agency for Toxic Substances and Disease
Registry.
[FR Doc. 2012-2971 Filed 2-8-12; 8:45 am]
BILLING CODE 4163-18-P