Agency Forms Undergoing Paperwork Reduction Act Review, 46631-46633 [2020-16795]
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<![CDATA[
46631
Federal Register / Vol. 85, No. 149 / Monday, August 3, 2020 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Form name
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Shigellosis case patients identified as part of
outbreak or cluster investigations.
Shigella Hypothesis Generating Questionnaire.
1500
1
45/60
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–16796 Filed 7–31–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[Docket No. CDC–2020–0070]
Proposed Data Collection Submitted
for Public Comment and
Recommendations: Extension of
Comment Period
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice.
public comment and recommendations
on a proposed data collection titled CDC
Diabetes Prevention Recognition
Program (OMB Control Number 0920–
0909) (85 FR 36214). Since then, CDC
has received a request to extend the
comment period to permit participants
in four regional Tribal consultation calls
to provide comment on this proposed
data collection. Four consultation calls
are scheduled for after August 14, 2020,
the original closing date of the docket.
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Science, Office of Scientific Integrity,
Centers for Disease Control and Prevention.
[FR Doc. 2020–16798 Filed 7–31–20; 8:45 am]
BILLING CODE 4163–18–P
AGENCY:
The Centers for Disease
Control and Prevention (CDC)within the
Department of Health and Human
Services (HHS) announces the extension
of the comment period for CDC Docket
Number CDC–2020–0070, CDC Diabetes
Prevention Recognition Program for an
additional 30 days.
DATES: Written comments must be
received on or before September 14,
2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2020–
0070 by either of the following methods.
CDC does not accept comment by email.
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Jeffrey Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS–D74, Atlanta,
Georgia 30329.
FOR FURTHER INFORMATION CONTACT:
Jeffrey Zirger, Information Collection
Review Office, Centers for Disease
Control and Prevention, 1600 Clifton
Road NE, MS–D74, Atlanta, Georgia
30329; phone: (404) 639–7118.
SUPPLEMENTARY INFORMATION: On June
15, 2020, as required by the Paperwork
Reduction Act, CDC published a notice
in the Federal Register requesting
khammond on DSKJM1Z7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
20:39 Jul 31, 2020
Jkt 250001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–20–20EU]
Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled Capacity
Building Assistance Program: Data
Management, Monitoring, and
Evaluation to the Office of Management
and Budget (OMB) for review and
approval. CDC previously published a
‘‘Proposed Data Collection Submitted
for Public Comment and
Recommendations’’ notice on January
28, 2020 to obtain comments from the
public and affected agencies. CDC did
not receive comments related to the
previous notice. This notice serves to
allow an additional 30 days for public
and affected agency comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
PO 00000
Frm 00046
Fmt 4703
Sfmt 4703
whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) 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 submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570.
Comments and recommendations for the
proposed information collection should
be sent within 30 days of publication of
this notice to www.reginfo.gov/public/
do/PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
Capacity Building Assistance
Program: Data Management, Monitoring,
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
E:\FR\FM\03AUN1.SGM
03AUN1
46632
Federal Register / Vol. 85, No. 149 / Monday, August 3, 2020 / Notices
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
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 six months from the program
managers within CDC-funded programs.
Program managers provide information
about the implementation status of the
intervention/public heath 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 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.
The total annualized burden is 1,671
hours. There are no other costs to
respondents other than their time.
khammond on DSKJM1Z7X2PROD with NOTICES
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Form name
Healthcare Professionals ................................
Healthcare Professionals ................................
Healthcare Professionals ................................
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 .................
VerDate Sep<11>2014
20:39 Jul 31, 2020
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Frm 00047
Fmt 4703
Sfmt 4703
E:\FR\FM\03AUN1.SGM
3,800
3,800
3,650
139
50
03AUN1
Number
responses per
respondent
1
2
2
2
2
Average
burden per
response
(in hours)
5/60
5/60
5/60
18/60
18/60
46633
Federal Register / Vol. 85, No. 149 / Monday, August 3, 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. 2020–16795 Filed 7–31–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–20–20QS; Docket No. CDC–2020–
0086]
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 Multi-site Clinical Assessment of
Myalgic Encephalomyelitis/Chronic
Fatigue Syndrome (MCAM). This
collection is designed to assess and
characterize illness heterogeneity of
Myalgic Encephalomyelitis/Chronic
Fatigue Syndrome (ME/CFS), and uses a
standardized approach including
standardized protocols with
standardized tests and instruments to
collect data on patients from multiple
clinical practices.
DATES: CDC must receive written
comments on or before October 2, 2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2020–
0086 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
SUMMARY:
• 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.
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:
404–639–7118; 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,
FOR FURTHER INFORMATION CONTACT:
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
Multi-site Clinical Assessment of
Myalgic Encephalomyelitis/Chronic
Fatigue Syndrome (MCAM)—Existing
collection in use without an OMB
Control Number—National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
This Multi-site Clinical Assessment of
Myalgic Encephalomyelitis/Chronic
Fatigue Syndrome (MCAM) study uses a
standardized approach for data
collection to examine the heterogeneity
of patients with Myalgic
Encephalomyelitis/Chronic Fatigue
Syndrome (ME/CFS) using a clinical
epidemiologic longitudinal study with a
retrospective and prospective rolling
cohort design. The study also aims to
address the issue of ME/CFS case
definition and improve measures of
illness domains by using evidencebased data from multiple clinical
practices in the United States. Healthy
adults and those with illnesses that
share some features with ME/CFS were
enrolled in comparison groups.
Children and adolescents with ME/CFS
and healthy participants were also
enrolled.
The MCAM study has been conducted
in multiple stages following multiple
study protocols. The time burden
estimates are based on the 2012–2019
data collection, which is the most recent
stage of data collection completed.
khammond on DSKJM1Z7X2PROD with NOTICES
ESTIMATED ANNUALIZED BURDEN HOURS
Type of
respondents
Adult
Adult
Adult
Adult
Adult
..............
..............
..............
..............
..............
VerDate Sep<11>2014
Number of
respondents
Form name
CDC Symptom Inventory (CDC–SI)/Form A .......................
CDC Symptom Inventory (CDC–SI)/Form B .......................
CDC Symptom Inventory (CDC–SI) ....................................
Short Form CDC–SI/Checklist .............................................
Medical Outcomes Study Short Form 36 ............................
20:39 Jul 31, 2020
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Frm 00048
Fmt 4703
Sfmt 4703
Average
burden
per
response
(in hours)
Number of
responses
per
respondent
45
20
20
85
85
E:\FR\FM\03AUN1.SGM
1
1
1
1
1
03AUN1
12/60
10/60
8/60
10/60
7/60
Total
burden
(in hours)
9
3
3
14
10
]]>Agencies
[Federal Register Volume 85, Number 149 (Monday, August 3, 2020)]
[Notices]
[Pages 46631-46633]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-16795]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-20-20EU]
Agency Forms Undergoing Paperwork Reduction Act Review
In accordance with the Paperwork Reduction Act of 1995, the Centers
for Disease Control and Prevention (CDC) has submitted the information
collection request titled Capacity Building Assistance Program: Data
Management, Monitoring, and Evaluation to the Office of Management and
Budget (OMB) for review and approval. CDC previously published a
``Proposed Data Collection Submitted for Public Comment and
Recommendations'' notice on January 28, 2020 to obtain comments from
the public and affected agencies. CDC did not receive comments related
to the previous notice. This notice serves to allow an additional 30
days for public and affected agency comments.
CDC will accept all comments for this proposed information
collection project. The Office of Management and Budget is particularly
interested in comments that:
(a) 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;
(b) Evaluate the accuracy of the agencies estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and clarity of the information to
be collected;
(d) 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 submission of responses; and
(e) Assess information collection costs.
To request additional information on the proposed project or to
obtain a copy of the information collection plan and instruments, call
(404) 639-7570. Comments and recommendations for the proposed
information collection should be sent within 30 days of publication of
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function. Direct
written comments and/or suggestions regarding the items contained in
this notice to the Attention: CDC Desk Officer, Office of Management
and Budget, 725 17th Street NW, Washington, DC 20503 or by fax to (202)
395-5806. Provide written comments within 30 days of notice
publication.
Proposed Project
Capacity Building Assistance Program: Data Management, Monitoring,
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
[[Page 46632]]
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 six
months from the program managers within CDC-funded programs. Program
managers provide information about the implementation status of the
intervention/public heath 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 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.
The total annualized burden is 1,671 hours. There are no other
costs to respondents other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number Average burden
Type of respondent Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Healthcare Professionals.............. Learning Group 3,800 1 5/60
Registration.
Healthcare Professionals.............. Post-Training Evaluation 3,800 2 5/60
Healthcare Professionals.............. Post-Technical 3,650 2 5/60
Assistance Evaluation.
Program Managers...................... Training and TA Follow- 139 2 18/60
up Survey.
Program Managers...................... Training and TA 50 2 18/60
Telephone Script.
----------------------------------------------------------------------------------------------------------------
[[Page 46633]]
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2020-16795 Filed 7-31-20; 8:45 am]
BILLING CODE 4163-18-P
