Proposed Information Collection Activity; Comment Request, 788 [2010-33241]
Download as PDF
788
Federal Register / Vol. 76, No. 4 / Thursday, January 6, 2011 / Notices
Purpose: The committee provides
advice and guidance to the Secretary,
HHS; the Assistant Secretary for Health;
and the Director, CDC, regarding the
formative research, development,
implementation and evaluation of
evidence-based activities designed to
prevent breast cancer (particularly
among those at heightened risk) and
promote the early detection and support
of young women who develop the
disease. The advice provided by the
Committee will assist in ensuring
scientific quality, timeliness, utility, and
dissemination of credible appropriate
messages and resource materials.
Matters To Be Discussed: The agenda
will include discussions on evidencebased recommendations and the public
health aspects of breast cancer in young
women including biology, genomics,
prevention, early diagnosis, treatment,
and survivorship; appropriate venues to
educate women at increased risk for
developing breast cancer at younger
ages; and approaches to increase
awareness of clinicians/practitioners
regarding topics such as breast health,
symptoms, diagnosis, and treatment of
breast cancer in young women.
Agenda items are subject to change as
priorities dictate.
In order to assure that sufficient space
and materials are available for meeting
attendees, CDC is requesting that
potential attendees register to attend
this meeting at the following Web site:
https://www.cdc.gov/cancer/breast/
what_cdc_is_doing/conference.htm.
Contact Person for More Information:
Temeika L. Fairley, PhD, Designated
Federal Officer, National Center for
Chronic Disease Prevention and Health
Promotion, CDC, 5770 Buford Hwy, NE.,
Mailstop K52, Atlanta, Georgia, 30341,
Telephone (770) 488–4518, Fax (770)
488–4760.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both the
Centers for Disease Control and
Prevention, and Agency for Toxic
Substances and Disease Registry.
Dated: December 28, 2010.
Elaine Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2011–26 Filed 1–5–11; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Title: National Survey of Child and
Adolescent Well-Being—Second Cohort
(NSCAW II).
OMB No.: 0970–0202.
Billing Accounting Code (BAC):
418422 (G994426).
Description: The Department of
Health and Human Services (HHS)
intends to collect follow-up data on a
sample of children and families for the
National Survey of Child and
Adolescent Wellbeing (NSCAW). The
NSCAW was authorized under Section
427 of the Personal Responsibility and
Work Opportunities Reconciliation Act
of 1996. The NSCAW is the only source
of nationally representative, firsthand
information about the functioning and
well-being, service needs, and service
utilization of children and families who
come to the attention of the child
welfare system. Information is collected
about children’s cognitive, social,
emotional, behavioral, and adaptive
functioning, as well as family and
community factors that are likely to
influence their functioning. Family
service needs and service utilization
also are addressed in the data collection.
Selection of the current NSCAW
sample and baseline data collection
began in 2007 with a final sample size
of 5,873 children. The proposed data
collection will allow for follow-up of
this sample 36 months post-baseline,
will follow the same format as that used
in the baseline round and the 18-month
follow-up, and will employ, with only
modest revisions, the same instruments
that were used in the previous rounds.
Data from NSCAW are made available to
the research community through
licensing arrangements from the
National Data Archive on Child Abuse
and Neglect at Cornell University.
Respondents: Children and their
associated permanent or foster
caregivers, caseworkers, and teachers.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
erowe on DSK5CLS3C1PROD with NOTICES
Child Interview .................................................................................................
Caregiver Interview ..........................................................................................
Caseworker Interview ......................................................................................
Teacher Questionnaire ....................................................................................
Estimated Total Annual Burden
Hours: 5, 882
In compliance with the requirements
of Section 3506(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 Planning, Research
and Evaluation, 370 L’Enfant
Promenade, SW., Washington, DC
VerDate Mar<15>2010
15:07 Jan 05, 2011
Jkt 223001
1,424
1,424
285
855
20447, Attn: OPRE Reports Clearance
Officer. E-mail address:
OPREinfocollection@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)
PO 00000
Frm 00019
Fmt 4703
Sfmt 9990
Number of
responses per
respondent
Average
burden hours
per response
1
1
3
1
Total burden
hours
1.33
1.9
1
.50
1,894
2,704
855
428
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: December 29, 2010.
Steven M. Hanmer,
Reports Clearance Officer.
[FR Doc. 2010–33241 Filed 1–5–11; 8:45 am]
BILLING CODE 4184–01–M
E:\FR\FM\06JAN1.SGM
06JAN1
Agencies
[Federal Register Volume 76, Number 4 (Thursday, January 6, 2011)]
[Notices]
[Page 788]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-33241]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Title: National Survey of Child and Adolescent Well-Being--Second
Cohort (NSCAW II).
OMB No.: 0970-0202.
Billing Accounting Code (BAC): 418422 (G994426).
Description: The Department of Health and Human Services (HHS)
intends to collect follow-up data on a sample of children and families
for the National Survey of Child and Adolescent Wellbeing (NSCAW). The
NSCAW was authorized under Section 427 of the Personal Responsibility
and Work Opportunities Reconciliation Act of 1996. The NSCAW is the
only source of nationally representative, firsthand information about
the functioning and well-being, service needs, and service utilization
of children and families who come to the attention of the child welfare
system. Information is collected about children's cognitive, social,
emotional, behavioral, and adaptive functioning, as well as family and
community factors that are likely to influence their functioning.
Family service needs and service utilization also are addressed in the
data collection.
Selection of the current NSCAW sample and baseline data collection
began in 2007 with a final sample size of 5,873 children. The proposed
data collection will allow for follow-up of this sample 36 months post-
baseline, will follow the same format as that used in the baseline
round and the 18-month follow-up, and will employ, with only modest
revisions, the same instruments that were used in the previous rounds.
Data from NSCAW are made available to the research community through
licensing arrangements from the National Data Archive on Child Abuse
and Neglect at Cornell University.
Respondents: Children and their associated permanent or foster
caregivers, caseworkers, and teachers.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average
Instrument Number of responses per burden hours Total burden
respondents respondent per response hours
----------------------------------------------------------------------------------------------------------------
Child Interview................................. 1,424 1 1.33 1,894
Caregiver Interview............................. 1,424 1 1.9 2,704
Caseworker Interview............................ 285 3 1 855
Teacher Questionnaire........................... 855 1 .50 428
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 5, 882
In compliance with the requirements of Section 3506(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
Planning, Research and Evaluation, 370 L'Enfant Promenade, SW.,
Washington, DC 20447, Attn: OPRE Reports Clearance Officer. E-mail
address: OPREinfocollection@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: December 29, 2010.
Steven M. Hanmer,
Reports Clearance Officer.
[FR Doc. 2010-33241 Filed 1-5-11; 8:45 am]
BILLING CODE 4184-01-M