Agency Forms Undergoing Paperwork Reduction Act Review, 15728-15729 [E9-7789]
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15728
Federal Register / Vol. 74, No. 65 / Tuesday, April 7, 2009 / Notices
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
IAATP: Trainee Survey Pre-Test Administration .............................................
IAATP: Trainee Survey Follow-Up Administration ...........................................
Estimated Total Annual Burden
Hours: 300.
In compliance with the requirements
of Section 506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, Office of Administration,
Office of Information Services, 370
L’Enfant Promenade, SW., Washington,
DC 20447, Attn: ACF Reports Clearance
Officer. E-mail address:
infocollection@acf.hhs.gov. All requests
should be identified by the title of the
information collection.
The Department specifically requests
comments on: (a) Whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
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.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Dated: April 2, 2009.
Janean Chambers,
Reports Clearance Officer.
[FR Doc. E9–7841 Filed 4–6–09; 8:45 am]
BILLING CODE 4184–01–P
Number of
responses per
respondent
1,200
1,200
1
1
Average
burden hours
per
response
0.15
0.10
Total burden
hours
180
120
cancers, and other health problems after
being treated for cancer. Research
evidence suggests that these elevated
risks can be mitigated by healthy
lifestyle practices and by undergoing
regular medical follow-up and cancer
screenings, however, little is known
about the factors that motivate or hinder
the adoption of recommended cancer
prevention and screening behaviors in
this population.
CDC proposes to conduct a survey of
five-year CRC survivors to collect
information about knowledge, attitudes,
psychosocial factors, health status and
behaviors, and utilization of health care
services including screening services.
Potential survey respondents will be
identified through California Cancer
Registry records. Each physician
associated with one or more CRC
patients will be responsible for
reviewing a customized list of names to
identify patients who should not be
contacted for recruitment into the study.
Following receipt of physician
permission to contact potential
participants, and receipt of participant
consent, 1,000 respondents will
complete a survey of health behaviors.
Approximately 900 respondents are
expected to complete a selfadministered survey that will be
delivered and returned by mail, and 100
respondents are expected to complete
the survey by computer-assisted
telephone interview, in response to a
follow-up call from study staff. OMB
clearance is being requested for one year
of data collection.
Findings from this study will help
guide future policies, programs, and
interventions developed to enhance and
improve the long-term health and well
being of cancer survivors.
There are no costs to respondents
except the time to complete the survey.
The total estimated burden hours are
1,095.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day-09–08BJ]
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.
Proposed Project
A Study of Primary and Secondary
Prevention Behaviors Practiced Among
Five-Year Survivors of Colorectal
Cancer—New—National Center for
Chronic Disease Prevention and Control
(NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Colorectal cancer (CRC) is the third
most prevalent cancer and the second
leading cause of cancer death in both
men and women in the United States. In
2004, there were an estimated 145,083
new cases of colorectal cancer
diagnosed and 53,580 deaths. However,
the five-year relative survival rates of
patients diagnosed with CRC have been
steadily increasing since 1975 and there
are now over one million CRC survivors
in the U.S.
Despite improved survival rates, CRC
survivors are at an elevated risk for
cancer recurrence, second primary
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondents
Form name
Physicians .........................................
List of Potential Study Participants ..
VerDate Nov<24>2008
17:13 Apr 06, 2009
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Frm 00040
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
1,950
E:\FR\FM\07APN1.SGM
1
07APN1
Average
burden per
response
(in hours)
13/60
Total burden
(in hours)
423
15729
Federal Register / Vol. 74, No. 65 / Tuesday, April 7, 2009 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Form name
CRC Survivors ..................................
Script for CATI Follow-up .................
Survey of Health Behaviors .............
Dated: April 1, 2009.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E9–7789 Filed 4–6–09; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration
Agency Information Collection
Activities: Proposed Collection;
Comment Request
In compliance with Section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 concerning
opportunity for public comment on
proposed collections of information, the
Substance Abuse and Mental Health
Services Administration (SAMHSA)
will publish periodic summaries of
proposed projects. To request more
information on the proposed projects or
to obtain a copy of the information
collection plans, call the SAMHSA
100
1,000
1
1
Reports Clearance Officer on (240) 276–
1243.
Comments are invited on: (a) Whether
the proposed collections of information
are necessary for the proper
performance of the functions of the
agency, including whether the
information shall have practical utility;
(b) the accuracy of the 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: 2010 National Survey
on Drug Use and Health—(OMB No.
0930–0110)—Revision
The National Survey on Drug Use and
Health (NSDUH) is a survey of the
civilian, non-institutionalized
population of the United States 12 years
old and older. The data are used to
determine the prevalence of use of
tobacco products, alcohol, illicit
substances, and illicit use of
3/60
40/60
Total burden
(in hours)
5
667
prescription drugs. The results are used
by SAMHSA, ONDCP, Federal
government agencies, and other
organizations and researchers to
establish policy, direct program
activities, and better allocate resources.
The 2010 NSDUH will continue
conducting a follow-up clinical
interview with a subsample of
approximately 500 respondents. The
design of this study is based on the
recommendations from a panel of expert
consultants convened by the Center for
Mental Health Services (CMHS),
SAMHSA, to discuss mental health
surveillance data collection strategies.
The goal is to create a statistically sound
measure that may be used to estimate
the prevalence of Serious Mental Illness
(SMI) among adults (age 18+).
For the 2010 NSDUH, no
questionnaire changes are proposed.
As with all NSDUH/NHSDA surveys
conducted since 1999, the sample size
of the survey for 2010 will be sufficient
to permit prevalence estimates for each
of the fifty states and the District of
Columbia. The total annual burden
estimate is shown below:
Average
burden per
response
(hr.)
Responses
per
respondent
Number of
responses
Household Screening ....................................................................................
Interview .........................................................................................................
Clinical Follow-up Interview ...........................................................................
Screening Verification ....................................................................................
Interview Verification ......................................................................................
Average
burden per
response
(in hours)
Number of
responses per
respondent
Number of
respondents
Type of respondents
Total burden
(hrs)
Dated: April 1, 2009.
Elaine Parry,
Director, Office of Program Services.
[FR Doc. E9–7788 Filed 4–6–09; 8:45 am]
BILLING CODE 4162–20–P
17:13 Apr 06, 2009
Jkt 217001
.083
1.0
1.0
0.067
0.067
15,836
67,500
500
362
678
........................
..........................
84,876
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration on Aging
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Semi-Annual and
Final Reporting Requirements for
Older Americans Act Title IV
Discretionary Grant Program
AGENCY:
ACTION:
VerDate Nov<24>2008
1
1
1
1
1
190,800
Send comments to Summer King,
SAMHSA Reports Clearance Officer,
Room 7–1044, One Choke Cherry Road,
Rockville, MD 20857 and e-mail her a
copy at summer.king@samhsa.hhs.gov.
Written comments should be received
within 60 days of this notice.
190,800
67,500
500
5,400
10,125
PO 00000
Administration on Aging, HHS.
Notice.
Frm 00041
Fmt 4703
Sfmt 4703
SUMMARY: The Administration on Aging
(AoA) is announcing an opportunity for
public comment on the proposed
collection of certain information by the
agency. Under the Paperwork Reduction
Act of 1995 (the PRA), Federal agencies
are required to publish notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information, and
to allow 60 days for public comment in
response to the notice. This notice
solicits comments on the information
E:\FR\FM\07APN1.SGM
07APN1
Agencies
[Federal Register Volume 74, Number 65 (Tuesday, April 7, 2009)]
[Notices]
[Pages 15728-15729]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-7789]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-09-08BJ]
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
A Study of Primary and Secondary Prevention Behaviors Practiced
Among Five-Year Survivors of Colorectal Cancer--New--National Center
for Chronic Disease Prevention and Control (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Colorectal cancer (CRC) is the third most prevalent cancer and the
second leading cause of cancer death in both men and women in the
United States. In 2004, there were an estimated 145,083 new cases of
colorectal cancer diagnosed and 53,580 deaths. However, the five-year
relative survival rates of patients diagnosed with CRC have been
steadily increasing since 1975 and there are now over one million CRC
survivors in the U.S.
Despite improved survival rates, CRC survivors are at an elevated
risk for cancer recurrence, second primary cancers, and other health
problems after being treated for cancer. Research evidence suggests
that these elevated risks can be mitigated by healthy lifestyle
practices and by undergoing regular medical follow-up and cancer
screenings, however, little is known about the factors that motivate or
hinder the adoption of recommended cancer prevention and screening
behaviors in this population.
CDC proposes to conduct a survey of five-year CRC survivors to
collect information about knowledge, attitudes, psychosocial factors,
health status and behaviors, and utilization of health care services
including screening services. Potential survey respondents will be
identified through California Cancer Registry records. Each physician
associated with one or more CRC patients will be responsible for
reviewing a customized list of names to identify patients who should
not be contacted for recruitment into the study. Following receipt of
physician permission to contact potential participants, and receipt of
participant consent, 1,000 respondents will complete a survey of health
behaviors. Approximately 900 respondents are expected to complete a
self-administered survey that will be delivered and returned by mail,
and 100 respondents are expected to complete the survey by computer-
assisted telephone interview, in response to a follow-up call from
study staff. OMB clearance is being requested for one year of data
collection.
Findings from this study will help guide future policies, programs,
and interventions developed to enhance and improve the long-term health
and well being of cancer survivors.
There are no costs to respondents except the time to complete the
survey. The total estimated burden hours are 1,095.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
Physicians.................... List of 1,950 1 13/60 423
Potential Study
Participants.
[[Page 15729]]
CRC Survivors................. Script for CATI 100 1 3/60 5
Follow-up.
Survey of Health 1,000 1 40/60 667
Behaviors.
----------------------------------------------------------------------------------------------------------------
Dated: April 1, 2009.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E9-7789 Filed 4-6-09; 8:45 am]
BILLING CODE 4163-18-P