60 day FRN

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Federal Register / Vol. 81, No. 143 / Tuesday, July 26, 2016 / Notices

work, the focus of their work and the
population groups and geographic areas
served.
The evaluation instruments are used
to assess training and capacity-building
outcomes (knowledge, confidence,
intention to use information, actual
changes made as a result of training)
immediately after and again 90 days

after training events. The evaluation
instruments vary based on the type of
training offered and take between
approximately 16 minutes to complete
(for intensive multi-day trainings) to 2
minutes to complete (for short didactic
or webinar sessions).
The CDC’s Funding Opportunity
Announcement PS 14–1407, NNPTC,

requires the collection of national
demographic information on grantees’
trainees and national evaluation
outcomes.
There are no costs to respondents
other than their time. The estimated
annualized burden hours for this data
collection are 502 hours.

ESTIMATES OF ANNUALIZED BURDEN
Number of
espondents

Average
urden per
esponse
(in hours)

Total burden
hours

Form name

Healthcare Professionals ..................

4,500

1

3/60

225

116

1

16/60

31

36

1

10/60

6

166

1

10/60

28

58

1

7/60

7

70
20
40
15
548

1
1
1
1
1

4/60
3/60
3/60
2/60
6/60

5
1
2
1
55

180

1

5/60

15

500

1

3/60

25

160

1

3/60

8

150
50
4,500

1
1
1

2/60
2/60
1/60

5
2
75

Healthcare Professionals ..................

NNPTC Abbreviated Health Professional Application for Training
(HPAT).
Intensive Complete Post-Course
Evaluation.
Intensive
Complete
Long-Term
Evaluation.
Intensive-Didactic Post-Course Evaluation.
Intensive-Didactic Long-Term Evaluation.
Practicum Post-Course Evaluation ..
Practicum Long-Term Evaluation .....
Wet Mount Post-Course Evaluation
Wet Mount Long-Term Evaluation ...
STD Tx Guidelines Complete PostCourse Evaluation.
STD Tx Guidelines Complete LongTerm Evaluation.
Short Guidelines Post-Course Evaluation.
Short Guidelines Long-Term Evaluation.
Basic Post-Course Evaluation .........
Basic Long-Term Evaluation ............
Immediate Post-Course email invitation.
3 Month Long-Term email invitation

660

1

1/60

11

Total ...........................................

...........................................................

........................

........................

........................

502

Healthcare Professionals ..................

Healthcare Professionals ..................

Healthcare Professionals ..................
Healthcare Professionals ..................
Healthcare Professionals ..................

Healthcare Professionals ..................

Healthcare Professionals ..................
Healthcare Professionals ..................

Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

[FR Doc. 2016–17603 Filed 7–25–16; 8:45 am]

[60Day–16–0612; Docket No. CDC–2016–
0070]

BILLING CODE 4163–18–P

Centers for Disease Control and
Prevention

Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice.
AGENCY:

srobinson on DSK5SPTVN1PROD with NOTICES

Number
esponses per
respondent

Type of respondent

The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal

SUMMARY:

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agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on the Well-Integrated
Screening and Evaluation for Women
Across the Nation (WISEWOMAN)
Reporting System. The WISEWOMAN
program aims to reduce cardiovascular
disease in women ages 40–64 by
providing screening services, referrals to
medical care, and lifestyle intervention
programs.
Written comments must be
received on or before September 26,
2016.

DATES:

You may submit comments,
identified by Docket No. CDC–2016–
0070 by any of the following methods:

ADDRESSES:

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srobinson on DSK5SPTVN1PROD with NOTICES

Federal Register / Vol. 81, No. 143 / Tuesday, July 26, 2016 / Notices
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE., MS–
D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov. Please note: All public
comment should be submitted through
the Federal eRulemaking portal
(Regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact the Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE., MS–D74, Atlanta,
Georgia 30329; phone: 404–639–7570;
Email: [email protected].
SUPPLEMENTARY INFORMATION:
Under the Paperwork Reduction Act
of 1995 (PRA) (44 U.S.C. 3501–3520),
Federal agencies must obtain approval
from the Office of Management and
Budget (OMB) for each collection of
information they conduct or sponsor. In
addition, the PRA also requires Federal
agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each new proposed
collection, each proposed extension of
existing collection of information, and
each reinstatement of previously
approved information collection before
submitting the collection to OMB for
approval. To comply with this
requirement, we are publishing this
notice of a proposed data collection as
described below.
Comments are invited 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)
ways to enhance the quality, utility, and
clarity of the information to be

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collected; (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; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.
Proposed Project
Well-Integrated Screening and
Evaluation for Women across the Nation
(WISEWOMAN) Reporting System
(OMB No. 0920–0612, exp. 12/31/
2016)—Extension—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The WISEWOMAN program (WellIntegrated Screening and Evaluation for
Women Across the Nation), sponsored
by the CDC, was established to examine
ways to improve the delivery of services
for women who have limited access to
health care and elevated risk factors for
cardiovascular disease (CVD). The
program focuses on reducing CVD risk
factors and provides screening services
for selected risk factors such as elevated
blood cholesterol, hypertension, and
abnormal blood glucose levels. The
program also provides women with
referrals to lifestyle programs and
medical care. The WISEWOMAN
program provides services to women
who are jointly enrolled in the National
Breast and Cervical Cancer Early
Detection Program (NBCCEDP), also
administered by CDC.
The WISEWOMAN program is
administered by state health
departments and tribal programs. In

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48807

2013, new cooperative agreements were
awarded under Funding Opportunity
Announcement DP13–1302. These
awards are currently in the final year of
funding, but may be extended by CDC
for one additional year, subject to the
availability of funds.
CDC collects two types of information
from WISEWOMAN awardees. The
hardcopy Annual Progress Report
provides a narrative summary of each
awardee’s objectives and the activities
undertaken to meet program goals. The
estimated burden per response is 16
hours.
In addition, each WISEWOMAN
awardee submits an electronic data file
to CDC twice per year. The Minimum
Data Elements (MDE) file contains deidentified, client-level information
about the cardiovascular disease risk
factors of women served by the program,
and the number and type of lifestyle
program sessions they attend. The
estimated burden per response for the
MDE file is 24 hours.
CDC seeks a one-year extension to
enable reporting for the final year of
activities funded under the current
cooperative agreement and the option
year, subject to the availability of funds.
There are no changes to the information
collected, the burden per response,
reporting frequency, the number of
awardees, or the total annualized
burden hours.
CDC will continue to use the
information collected from
WISEWOMAN awardees to support
program monitoring and improvement
activities, evaluation, and assessment of
program outcomes. The overall program
evaluation is designed to demonstrate
how WISEWOMAN can obtain more
complete health data on vulnerable
populations, promote public education
about disease incidence, cardiovascular
disease risk-factors, health promotion,
improve the availability of screening
and diagnostic services for under-served
women, ensure the quality of services
provided to underserved women, and
develop strategies for improved
interventions.
OMB approval is requested for one
year. Participation in this information
collection is required as a condition of
cooperative agreement funding. There
are no costs to respondents other than
their time. The total annualized burden
hours are 1,344.

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Federal Register / Vol. 81, No. 143 / Tuesday, July 26, 2016 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent

Number of
respondents

Average
burden per
response
(in hrs.)

Total burden
(in hrs.)

Type of respondents

Form name

WISEWOMAN Awardees ..................

Screening and Assessment and
Lifestyle Program MDEs.
Annual Progress Report ...................

21

2

24

1,008

21

1

16

336

...........................................................

........................

........................

........................

1,344

Total ...........................................

Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2016–17602 Filed 7–25–16; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Phase II Evaluation Activities
for Implementing a Next Generation

Evaluation Agenda for the Chafee Foster
Care Independence Program.
OMB No.: New Collection.
Description: The Administration for
Children and Families (ACF), Office of
Planning Research and Evaluation
(OPRE) is proposing an information
collection activity as part of the Phase
II Evaluation Activities for
Implementing a Next Generation
Evaluation Agenda for the Chafee Foster
Care Independence Program. The
proposed information collection
consists of site visits by staff from the
Urban Institute and Chapin Hall at the
University of Chicago to conduct
formative evaluations of programs
serving transition-age foster youth. The
evaluations will include preliminary

visits to discuss the evaluation process
with program administrators. Then, the
research team will conduct site visits to
each program to speak with program
leaders, partners and key stakeholders,
front-line staff, and participants. These
formative evaluations will determine
programs’ readiness for more rigorous
evaluation in the future. The activities
and products from this project will help
ACF to fulfill their ongoing legislative
mandate for program evaluation
specified in the Foster Care
Independence Act of 1999.
Respondents: Program leaders,
partners and stakeholders, and frontline
staff as well as young adults being
served by the programs.

ANNUAL BURDEN ESTIMATES
Total number
of respondents

Instrument

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Outreach email for discussion with program admin and
staff ...................................................................................
Outreach email for Focus Group Recruiters .......................
Informed Consent and Discussion Guide for program leaders .....................................................................................
Informed Consent and Discussion Guide for program partners and stakeholders ......................................................
Informed Consent and Discussion Guide for program
front-line staff ....................................................................
Informed Consent and Focus Group Guide for program
participants .......................................................................
Compilation and Submission of Administrative Data ..........

Estimated Total Annual Burden
Hours: 800.
Additional Information: Copies of the
proposed collection may be obtained by
writing to the Administration for
Children and Families, Office of
Planning, Research and Evaluation, 330
C Street SW., Washington, DC 20201,
Attn: OPRE Reports Clearance Officer.
All requests should be identified by the
title of the information collection. Email
address: OPREinfocollection@
acf.hhs.gov.
OMB Comment: OMB is required to
make a decision concerning the
collection of information between 30

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Annual
number of
respondents

Number of
responses per
respondent

Frm 00073

Fmt 4703

Annual burden
hours

16
16

8
8

1
1

1
8

8
64

48

24

4

1

96

80

40

2

1

80

128

64

1

1

64

200
24

100
12

1
2

2
12

200
288

and 60 days after publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect if OMB receives it
within 30 days of publication. Written
comments and recommendations for the
proposed information collection should
be sent directly to the following: Office
of Management and Budget, Paperwork
Reduction Project, Email: OIRA_
[email protected], Attn:

PO 00000

Average
burden hours
per response

Sfmt 9990

Desk Officer for the Administration for
Children and Families.
Robert Sargis,
ACF Certifying Officer.
[FR Doc. 2016–17618 Filed 7–25–16; 8:45 am]
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