Proposed Data Collection Submitted for Public Comment and Recommendations, 4988-4990 [2020-01387]
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4988
Federal Register / Vol. 85, No. 18 / Tuesday, January 28, 2020 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent
Individuals and
Households.
Average
burden per
response
(in hours)
958
1
3/60
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
Phase
333
389
389
667
427
211
29
667
40
27
27
14
13
22
29
14
2
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
3/60
3/60
3/60
40/60
25/60
25/60
40/60
25/60
1
3/60
3/60
3/60
3/60
40/60
25/60
25/60
40/60
2 Screener—ABS, web ...............................................................
2 Screener—ABS, paper—Roster method .................................
2 Screener—ABS, paper—YMOF Method .................................
2 Questionnaire—RDD (CATI) ....................................................
2—Questionnaire—ABS, web .....................................................
2 Questionnaire—ABS, paper .....................................................
2 Questionnaire—ABS, in-bound CATI ......................................
2 Questionnaire—Panel, web .....................................................
2 Cognitive Testing Protocol—Cognitive testing ........................
3 Screener—RDD (CATI) ...........................................................
3 Screener—ABS, web ...............................................................
3 Screener—ABS, paper—Roster method .................................
3 Screener ABS, paper—YMOF Method ....................................
3 Questionnaire—RDD (CATI) ....................................................
3 Questionnaire—ABS, web .......................................................
3 Questionnaire—ABS, paper .....................................................
3 Questionnaire—ABS, in-bound CATI ......................................
[FR Doc. 2020–01378 Filed 1–27–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–20–20EU; Docket No. CDC–2019–
0119]
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 with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled Capacity Building Assistance
Program: Data Management, Monitoring,
and Evaluation. The purpose of this data
collection is to evaluate the CDC
cooperative agreement program entitled
CDC–RFA–PS19–1904: Capacity
SUMMARY:
jbell on DSKJLSW7X2PROD with NOTICES
Number of
responses per
respondent
Phase 2 Screener—RDD (CATI) ...........................................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
VerDate Sep<11>2014
Number of
respondents
Form name
17:02 Jan 27, 2020
Jkt 250001
Building Assistance (CBA) for High
Impact HIV Prevention Program
Integration.
DATES: CDC must receive written
comments on or before March 30, 2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2019–
0119 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, 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. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
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 Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS–
D74, Atlanta, Georgia 30329; phone:
404–639–7570; Email: omb@cdc.gov.
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
PO 00000
Frm 00045
Fmt 4703
Sfmt 4703
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 the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses.
5. Assess information collection costs.
Proposed Project
Capacity Building Assistance
Program: Data Management, Monitoring,
E:\FR\FM\28JAN1.SGM
28JAN1
4989
Federal Register / Vol. 85, No. 18 / Tuesday, January 28, 2020 / Notices
and Evaluation—New—National Center
for HIV/AIDS, Viral Hepatitis, STD, and
TB Prevention (NCHHSTP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC) partners with the
national HIV prevention workforce to
(1) ensure that persons with HIV (PWH)
are aware of their infection and
successfully linked to medical care and
treatment to achieve viral suppression
and (2) expand access to pre-exposure
prophylaxis (PrEP), condoms, and other
proven strategies for persons at risk of
becoming infected. CDC funds state and
local health departments and
community-based organizations (CBOs)
to optimally plan, integrate, implement,
and sustain comprehensive HIV
prevention programs and services for
people with and at greatest risk of HIV
infection, including blacks/African
Americans; Hispanics/Latinos; all races/
ethnicities of gay, bisexual, and other
men who have sex with men (MSM);
people who inject drugs (PWID); and
transgender persons.
Through the CDC cooperative
agreement program entitled CDC–RFA–
PS19–1904: Capacity Building
Assistance (CBA) for High Impact HIV
Prevention Program Integration, the
CDC Division of HIV/AIDS Prevention
(DHAP) funds the CBA Provider
Network (CPN) to deliver CBA to CDCfunded health departments and CBOs.
CBA provided by the CPN include
trainings and technical assistance (TA)
that enable the HIV prevention
workforce to optimally plan, implement,
integrate, and sustain high-impact
prevention interventions and strategies
to reduce HIV infections and HIVrelated morbidity, mortality, and health
disparities across the United States and
its territories. This information
collection evaluates CDC–RFA–PS19–
1904. Specifically, the CDC is requesting
the Office of Management and Budget
(OMB) to grant a three-year approval to
collect data through the use of four webbased instruments that will be
under PS19–1904. The TTAFS will be
administered to the program managers
of state and local health department
staff and CBO staff who participate in a
CBA training or TA event. Respondents
will provide information electronically
through an online survey. The option to
complete surveys via a telephone
interview will be offered to respondents
who do not complete the online survey
within seven days.
The number of respondents is
calculated based on an average of the
number of health professionals,
including doctors, nurses, health
educators, and disease intervention
specialists, trained by CBA providers
during the years 2016–2018. We
estimate 3,800 health professionals will
provide one response for the Learning
Group Registration; 3,800 health
professionals will provide a response for
the PTE for each training episode; 3,650
health professionals will provide a
response for the PTAE for each TA
episode; and 189 program managers will
provide two responses to the TTAFS in
the web-based or telephone survey per
year. The total annualized burden is
1,671 hours. There are no other costs to
respondents other than their time.
The information collected will allow
CDC to:
(1) Identify and respond to public
health program performance issues
identified through feedback from health
departments and CBOs;
(2) Identify and respond to new HIV
prevention training and TA needs of
health departments and CBOs;
(3) Provide a timely and accurate
response to federal, state, and local
agencies and other stakeholders seeking
information about the types and quality
of CBA services delivered. No other
federal agency collects this type of
national HIV prevention capacity
building data.
CDC is requesting approval for an
estimated 1,671 burden hours annually.
There is no cost to respondents other
than their time.
administered to recipients of CBA
services and their program managers: (1)
Learning Group Registration; (2) PostTraining Evaluation (PTE); (3) PostTechnical Assistance Evaluation
(PTAE); and (4) Training and Technical
Assistance Follow-up Survey (TTAFS).
CBA training participants will
complete the Learning Group
Registration Form as part of the process
for enrolling in a CBA training. The
Learning Group Registration Form
collects demographic information about
training participants including: (1)
Business contact information (e.g., email
and telephone number); (2) primary
[employment] functional role; (3)
employment setting; and (4)
programmatic and population areas of
focus. After an online or in-person
training event is completed, training
participants are invited to complete the
PTE. The PTE is designed to elicit
information from training participants
about their satisfaction with the training
delivery method and course content.
Similar to the PTE, the PTAE consists
of questions designed to elicit
information from TA participants about
their satisfaction with aspects of TA
such as the relevance of the materials
provided or created, responsiveness of
the TA provider, TA participants’
changes in knowledge or skills as a
result of the TA, and barriers and
facilitators to implementation of
interventions/public health strategies.
The TTAFS collects organizational-level
data every 6 months from the program
managers within CDC-funded programs.
Program managers provide information
about the implementation status of the
intervention/public health strategy for
which their staff received training and/
or TA. Program managers are also asked
to describe how their organization
applied the training and TA (e.g.,
planning or adapting an intervention/
public health strategy).
The Learning Group Registration
Form, PTE, and PTAE will be
administered to CDC-funded program
staff who participate in a training or TA
event offered by a CBA provider funded
jbell on DSKJLSW7X2PROD with NOTICES
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number
responses per
respondent
Average
burden per
response
(in hours)
Total
burden hours
Type of respondent
Form name
Healthcare Professionals ..................
Healthcare Professionals ..................
Healthcare Professionals ..................
3,800
3,800
3,650
1
2
2
5/60
5/60
5/60
317
633
608
Program Managers ...........................
Program Managers ...........................
Learning Group Registration ............
Post-Training Evaluation ..................
Post-Technical Assistance Evaluation.
Training and TA Follow-up Survey ..
Training and TA Telephone Script ...
139
50
2
2
18/60
18/60
83
30
Total ...........................................
...........................................................
........................
........................
........................
1,671
VerDate Sep<11>2014
17:02 Jan 27, 2020
Jkt 250001
PO 00000
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Fmt 4703
Sfmt 4703
E:\FR\FM\28JAN1.SGM
28JAN1
4990
Federal Register / Vol. 85, No. 18 / Tuesday, January 28, 2020 / Notices
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–01387 Filed 1–27–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–20–0278; Docket No. CDC–2020–
0004]
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 with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled the National Hospital Ambulatory
Medical Care Survey (NHAMCS).
NHAMCS collects facility and visit
information on ambulatory care services
utilization in non-Federal, short stay
hospitals in the United States.
DATES: CDC must receive written
comments on or before March 30, 2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2020–
0004 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, 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. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
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
jbell on DSKJLSW7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:02 Jan 27, 2020
Jkt 250001
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS–
D74, Atlanta, Georgia 30329; phone:
404–639–7570; Email: omb@cdc.gov.
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 the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses.
5. Assess information collection costs.
Proposed Project
National Hospital Ambulatory
Medical Care Survey (NHAMCS) (OMB
Control No. 0920–0278, Exp. 06/30/
2021)—Revision—National Center for
Health Statistics (NCHS), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Section 306 of the Public Health
Service (PHS) Act (42 U.S.C. 242k), as
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
amended, authorizes that the Secretary
of Health and Human Services (DHHS),
acting through NCHS, shall collect
statistics on ‘‘utilization of health care’’
in the United States. The National
Hospital Ambulatory Medical Care
Survey (NHAMCS) has been conducted
annually since 1992. NCHS is seeking
OMB approval to extend this survey for
an additional three years.
The target universe of the NHAMCS is
in-person visits made to emergency
departments (EDs) of non-Federal, shortstay hospitals (hospitals with an average
length of stay of less than 30 days) that
have at least 6 beds for inpatient use,
and with a specialty of general (medical
or surgical) or children’s general.
NHAMCS was initiated to
complement the National Ambulatory
Medical Care Survey (NAMCS, OMB
No. 0920–0234, Exp. Date 05/31/2022),
which provides similar data concerning
patient visits to physicians’ offices.
NAMCS and NHAMCS are the principal
sources of data on ambulatory care
provided in the United States. NHAMCS
provides a range of baseline data on the
characteristics of the users and
providers of hospital ambulatory
medical care. Data collected include
patients’ demographic characteristics,
reason(s) for visit, providers’ diagnoses,
diagnostic services, medications, and
disposition. These data, together with
trend data, may be used to monitor the
effects of change in the health care
system, for the planning of health
services, improving medical education,
determining health care work force
needs, and assessing the health status of
the population.
Starting 2018, NHAMCS was
modified to assess only hospital
emergency departments. The survey
components that assessed hospital
outpatient departments and ambulatory
surgery locations were discontinued. No
substantive changes or supplements are
expected for the survey for the three
years being requested.
Users of NHAMCS data include, but
are not limited to, congressional offices,
Federal agencies, state and local
governments, schools of public health,
colleges and universities, private
industry, nonprofit foundations,
professional associations, clinicians,
researchers, administrators, and health
planners. There are no costs to the
respondents other than their time. The
total estimated annualized burden hours
are 1,124.
E:\FR\FM\28JAN1.SGM
28JAN1
]]>Agencies
[Federal Register Volume 85, Number 18 (Tuesday, January 28, 2020)]
[Notices]
[Pages 4988-4990]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-01387]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-20-20EU; Docket No. CDC-2019-0119]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing effort to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies the opportunity to comment on a proposed and/or
continuing information collection, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on a proposed
information collection project titled Capacity Building Assistance
Program: Data Management, Monitoring, and Evaluation. The purpose of
this data collection is to evaluate the CDC cooperative agreement
program entitled CDC-RFA-PS19-1904: Capacity Building Assistance (CBA)
for High Impact HIV Prevention Program Integration.
DATES: CDC must receive written comments on or before March 30, 2020.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2019-
0119 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Jeffrey M. Zirger, 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. CDC will post, without change, all relevant comments
to Regulations.gov.
Please note: Submit all comments 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 Jeffrey M. Zirger, 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 the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected; and
4. Minimize the burden of the collection of information on those
who are to respond, including through the use of appropriate automated,
electronic, mechanical, or other technological collection techniques or
other forms of information technology, e.g., permitting electronic
submissions of responses.
5. Assess information collection costs.
Proposed Project
Capacity Building Assistance Program: Data Management, Monitoring,
[[Page 4989]]
and Evaluation--New--National Center for HIV/AIDS, Viral Hepatitis,
STD, and TB Prevention (NCHHSTP), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and Prevention (CDC) partners with
the national HIV prevention workforce to (1) ensure that persons with
HIV (PWH) are aware of their infection and successfully linked to
medical care and treatment to achieve viral suppression and (2) expand
access to pre-exposure prophylaxis (PrEP), condoms, and other proven
strategies for persons at risk of becoming infected. CDC funds state
and local health departments and community-based organizations (CBOs)
to optimally plan, integrate, implement, and sustain comprehensive HIV
prevention programs and services for people with and at greatest risk
of HIV infection, including blacks/African Americans; Hispanics/
Latinos; all races/ethnicities of gay, bisexual, and other men who have
sex with men (MSM); people who inject drugs (PWID); and transgender
persons.
Through the CDC cooperative agreement program entitled CDC-RFA-
PS19-1904: Capacity Building Assistance (CBA) for High Impact HIV
Prevention Program Integration, the CDC Division of HIV/AIDS Prevention
(DHAP) funds the CBA Provider Network (CPN) to deliver CBA to CDC-
funded health departments and CBOs. CBA provided by the CPN include
trainings and technical assistance (TA) that enable the HIV prevention
workforce to optimally plan, implement, integrate, and sustain high-
impact prevention interventions and strategies to reduce HIV infections
and HIV-related morbidity, mortality, and health disparities across the
United States and its territories. This information collection
evaluates CDC-RFA-PS19-1904. Specifically, the CDC is requesting the
Office of Management and Budget (OMB) to grant a three-year approval to
collect data through the use of four web-based instruments that will be
administered to recipients of CBA services and their program managers:
(1) Learning Group Registration; (2) Post-Training Evaluation (PTE);
(3) Post-Technical Assistance Evaluation (PTAE); and (4) Training and
Technical Assistance Follow-up Survey (TTAFS).
CBA training participants will complete the Learning Group
Registration Form as part of the process for enrolling in a CBA
training. The Learning Group Registration Form collects demographic
information about training participants including: (1) Business contact
information (e.g., email and telephone number); (2) primary
[employment] functional role; (3) employment setting; and (4)
programmatic and population areas of focus. After an online or in-
person training event is completed, training participants are invited
to complete the PTE. The PTE is designed to elicit information from
training participants about their satisfaction with the training
delivery method and course content.
Similar to the PTE, the PTAE consists of questions designed to
elicit information from TA participants about their satisfaction with
aspects of TA such as the relevance of the materials provided or
created, responsiveness of the TA provider, TA participants' changes in
knowledge or skills as a result of the TA, and barriers and
facilitators to implementation of interventions/public health
strategies. The TTAFS collects organizational-level data every 6 months
from the program managers within CDC-funded programs. Program managers
provide information about the implementation status of the
intervention/public health strategy for which their staff received
training and/or TA. Program managers are also asked to describe how
their organization applied the training and TA (e.g., planning or
adapting an intervention/public health strategy).
The Learning Group Registration Form, PTE, and PTAE will be
administered to CDC-funded program staff who participate in a training
or TA event offered by a CBA provider funded under PS19-1904. The TTAFS
will be administered to the program managers of state and local health
department staff and CBO staff who participate in a CBA training or TA
event. Respondents will provide information electronically through an
online survey. The option to complete surveys via a telephone interview
will be offered to respondents who do not complete the online survey
within seven days.
The number of respondents is calculated based on an average of the
number of health professionals, including doctors, nurses, health
educators, and disease intervention specialists, trained by CBA
providers during the years 2016-2018. We estimate 3,800 health
professionals will provide one response for the Learning Group
Registration; 3,800 health professionals will provide a response for
the PTE for each training episode; 3,650 health professionals will
provide a response for the PTAE for each TA episode; and 189 program
managers will provide two responses to the TTAFS in the web-based or
telephone survey per year. The total annualized burden is 1,671 hours.
There are no other costs to respondents other than their time.
The information collected will allow CDC to:
(1) Identify and respond to public health program performance
issues identified through feedback from health departments and CBOs;
(2) Identify and respond to new HIV prevention training and TA
needs of health departments and CBOs;
(3) Provide a timely and accurate response to federal, state, and
local agencies and other stakeholders seeking information about the
types and quality of CBA services delivered. No other federal agency
collects this type of national HIV prevention capacity building data.
CDC is requesting approval for an estimated 1,671 burden hours
annually. There is no cost to respondents other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number Average burden
Type of respondent Form name Number of responses per per response Total burden
respondents respondent (in hours) hours
----------------------------------------------------------------------------------------------------------------
Healthcare Professionals...... Learning Group 3,800 1 5/60 317
Registration.
Healthcare Professionals...... Post-Training 3,800 2 5/60 633
Evaluation.
Healthcare Professionals...... Post-Technical 3,650 2 5/60 608
Assistance
Evaluation.
Program Managers.............. Training and TA 139 2 18/60 83
Follow-up
Survey.
Program Managers.............. Training and TA 50 2 18/60 30
Telephone
Script.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 1,671
----------------------------------------------------------------------------------------------------------------
[[Page 4990]]
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2020-01387 Filed 1-27-20; 8:45 am]
BILLING CODE 4163-18-P
