Agency Information Collection Activities: Proposed Collection; Comment Request, 36203-36205 [2020-12804]
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Federal Register / Vol. 85, No. 115 / Monday, June 15, 2020 / Notices
Notice of request for comments
regarding an extension to an OMB
clearance.
ACTION:
Under the provisions of the
Paperwork Reduction Act, the
Regulatory Secretariat Division will be
submitting to the Office of Management
and Budget (OMB) a request to review
and approve an extension of a
previously approved information
collection requirement regarding the
National Contact Center customer
evaluation surveys.
DATES: Submit comments on or before:
July 15, 2020.
FOR FURTHER INFORMATION CONTACT: Mr.
David Kaufmann, Program Analyst,
Office of Technology Transformation
Services, via email to david.kaufmann@
gsa.gov, or at 202–357–9661.
ADDRESSES: Written comments and
recommendations for this 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
Review—Open for Public Comments’’ or
by using the search function.
SUPPLEMENTARY INFORMATION:
SUMMARY:
A. Purpose
Beth Ann Killoran,
Deputy Chief Information Officer.
[FR Doc. 2020–12184 Filed 6–12–20; 8:45 am]
BILLING CODE 6820–CX–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Agency for Healthcare Research
and Quality, HHS.
AGENCY:
ACTION:
Notice.
This notice announces the
intention of the Agency for Healthcare
Research and Quality (AHRQ) to request
that the Office of Management and
Budget (OMB) approve the proposed
information collection project ‘‘AHRQ
Managing Unhealthy Alcohol Use in
Primary Care Initiative.’’ This proposed
information collection was previously
published in the Federal Register on
March 30, 2020 and allowed 60 days for
public comment. AHRQ did not receive
any comments during the
aforementioned public comment period.
The purpose of this notice is to allow an
additional 30 days for public comment.
SUMMARY:
This information collection will be
used to assess the public’s satisfaction
with the USA.gov National Contact
Center service (formerly the Federal
Citizen Information Center’s (FCIC)
National Contact Center), to assist in
increasing the efficiency in responding
to the public’s need for Federal
information, and to assess the
effectiveness of marketing efforts.
B. Annual Reporting Burden
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OBTAINING COPIES OF
PROPOSALS: Requesters may obtain a
copy of the information collection
documents from the GSA Regulatory
Secretariat Division (MVCB)by calling
202–501–4755, or emailing
GSARegSec@gsa.gov. Please cite OMB
Control No. 3090–0278, National
Contact Center Customer Evaluation
Survey, in all correspondence.
The following are estimates of the
annual hourly burdens for our surveys
based on historical participation in our
surveys.
(1) Telephone Survey:
Respondents: 6000.
Responses per Respondent: 1.
Annual Responses: 6000.
Hours per Response: 0.12.
Total Burden Hours: 720.
(2) Web Chat Survey:
Respondents: 2400.
Responses per Respondent: 1.
Annual Responses: 2400.
Hours Per Response: 0.12.
Total Burden Hours: 288.
Grand Total Burden Hours: 1008.
Comments on this notice must be
received by 30 days after date of
publication of this notice.
DATES:
Written 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.
ADDRESSES:
C. Public Comments
FOR FURTHER INFORMATION CONTACT:
A 60-day notice was published in the
Federal Register at 85 FR 17333 on
March 27, 2020. No comments were
received.
SUPPLEMENTARY INFORMATION:
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17:04 Jun 12, 2020
Jkt 250001
Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427–1477, or by
email at doris.lefkowitz@AHRQ.hhs.gov.
PO 00000
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36203
Proposed Project
AHRQ Managing Unhealthy Alcohol
Use in Primary Care Initiative
The Affordable Care Act established
the Patient-Centered Outcomes Research
Trust Fund (PCORTF) and authorized
AHRQ to broadly disseminate the
research findings published by the
Patient-Centered Outcomes Research
Institute (PCORI) and other governmentfunded research relevant to comparative
clinical effectiveness research. AHRQ’s
PCORTF-funded initiative identifies
research findings that could
significantly improve patient outcomes
through broader implementation in
clinical practice. Under this initiative,
in 2019 AHRQ launched a new
initiative, Managing Unhealthy Alcohol
Use in Primary Care, in order to
promote the uptake of evidence-based
practices for unhealthy alcohol use
(UAU). As part of this initiative, AHRQ
selected six grantees and funded a
contractor to support and evaluate the
grantees. The grantees will collectively
work with more than 700 primary care
practices over three years to implement
and evaluate strategies to increase the
use of evidence-based interventions
such as screening for unhealthy alcohol
use, brief interventions for adult
patients who drink too much, and
medication-assisted therapy (MAT) for
patients with an alcohol use disorder.
The contractor will develop a resource
center, convene a technical expert
panel, conduct an ongoing
environmental scan, support a learning
community of grantees, and complete a
multisite, mixed methods evaluation.
Unhealthy alcohol use, defined as
behaviors ranging from risky drinking to
alcohol use disorders (AUD), is
estimated to be the third leading cause
of preventable death in the United
States. Between 2006 and 2010, nearly
one in ten deaths were alcohol-related.
In addition to early mortality, UAU is
associated with a host of adverse
outcomes, including unintentional
injuries and the development or
exacerbation of a range of physical and
behavioral health conditions. The
Centers for Disease Control and
Prevention estimates suggest that
excessive alcohol consumption costs the
United States $249 billion annually.
Under the UAU initiative, six AHRQ
grantees will work to improve the
management of UAU in primary care by
disseminating and implementing
evidence-based practices for screening
and brief intervention, referral to
treatment (SBI/RT), and MAT in
primary care practices. The multi-site,
mixed-methods evaluation will include
primary data collection by the evaluator,
E:\FR\FM\15JNN1.SGM
15JNN1
36204
Federal Register / Vol. 85, No. 115 / Monday, June 15, 2020 / Notices
NORC at the University of Chicago. The
evaluation will also include secondary
data collected by the six grantee teams
working with 750 primary care
practices. Collectively the data will
allow the evaluator to assess the
implementation and impact of the six
grants.
The project goals, as laid out in the
AHRQ request for applications include:
• Success of recruitment and
retention strategies across all six
grantees to engage primary care
practices for implementation of SBI/RT
and MAT, across the initiative;
• Effectiveness of the grantees’
collective dissemination and
implementation strategies, and the
factors associated with the success and/
or failure of the strategies as it relates to
populations, settings and the influence
of contextual factors;
• Success at the practice level in
increasing the number of patients
screened, identified, and treated; and
• Overall impact on changes in
processes or outcomes that can be
attributed to the initiative.
This study is being conducted
pursuant to AHRQ’s statutory authority
to broadly disseminate research findings
published by the Patient-Centered
Outcomes Research Institute and other
government-funded research relevant to
comparative clinical effectiveness
research to physicians, health care
providers, and patients. 42 U.S.C 299b–
37.
Method of Collection
To achieve the goals of the multi-site
evaluation (MSE), AHRQ is requesting
OMB approval for three years for new
data collection by the evaluator. The
evaluator’s primary data collection is
requested to achieve the goals of the
MSE and includes the following data
collection activities:
Semi-Structured Qualitative
Interviews will take place in-person
and/or by telephone with key staff from
each grantee team (i.e., principal
investigator, co-investigator, evaluation
lead, practice facilitation/
implementation lead, and project
manager) and with clinicians and staff
at one primary care practice working
with each grantee. Interviews will be
conducted annually beginning at the
end of Year 1, for a total of three time
points per grantee. During Years 1 and
3 the interviews will be conducted by
phone, while Year 2 interviews will be
collected in-person. The interviews for
both grantee teams and primary care
practice staff will cover domains such as
understanding the practice
implementation and changes overtime,
methods of supporting practices,
barriers and facilitators to
implementation, strategies to overcome
barriers, and the number and type of
staff implementing SBI/RT and MAT.
Secondary data collected by grantees
and analyzed by the evaluator will
include:
Aggregated process measure data that
will be used to assess whether the
number of patients receiving SBI/RT
and/or MAT increased at the practice
level. Grantees will survey all
participating primary care practices at
the beginning of the initiative to collect
data on basic practice characteristics
(e.g., size, ownership, staff, and patient
population) that can be used to evaluate
relationships between practice
characteristics and the number of
patients receiving SBI/RT and/or MAT.
Grantees will also collect quantitative
information about the number, duration,
and function of contact between
practice facilitators and primary care
practices to evaluate the relationship
between duration, frequency, and type
of practice facilitator-practice
engagement, and the number of patients
screened, receiving brief intervention,
and/or treated for UAU. The practice
facilitators will collect data to track
changes in practices over time and
facilitate an overall assessment of what
activities the practice is conducting to
identify and manage UAU.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated
annualized burden hours for the
respondents’ time to complete the semistructured Key Informant Interviews.
For the three-year clearance period, the
estimated annualized burden hours for
the interviews are 60.
EXHIBIT 1
Number of
respondents
Data collection activity
Number of
responses per
respondent
Hours per
response
Total burden
hours
Semi-Structured Interviews ..............................................................................
60
1
1.0
60
Total ..........................................................................................................
60
........................
........................
60
Exhibit 2 shows the estimated
annualized cost burden based on the
respondents’ time to complete the Key
Informant Interviews. The total
annualized cost burden is estimated to
be $6,109.
EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN
Number of
respondents
jbell on DSKJLSW7X2PROD with NOTICES
Form name
Total burden
hours
Average
hourly wage
rate *
Total cost
burden
Semi-Structured Interviews ..............................................................................
60
60
a $101.82
$6,109
Total ..........................................................................................................
60
60
........................
6,109
* National Compensation Survey: Occupational wages in the United States May 2018 ‘‘U.S. Department of Labor, Bureau of Labor Statistics’’:
https://www.bls.gov/oes/current/oes_stru.htm.
a Based on the mean wages for 29–1062 Family and General Practitioners.
Request for Comments
In accordance with the Paperwork
Reduction Act, comments on AHRQ’s
VerDate Sep<11>2014
17:04 Jun 12, 2020
Jkt 250001
information collection are requested
with regard to any of the following: (a)
Whether the proposed collection of
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information is necessary for the proper
performance of AHRQ’s health care
research and health care information
E:\FR\FM\15JNN1.SGM
15JNN1
Federal Register / Vol. 85, No. 115 / Monday, June 15, 2020 / Notices
dissemination functions, including
whether the information will have
practical utility; (b) the accuracy of
AHRQ’s estimate of burden (including
hours and costs) of the proposed
collection(s) 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 upon the
respondents, including the use of
automated collection techniques or
other forms of information technology.
Comments submitted in response to
this notice will be summarized and
included in the Agency’s subsequent
request for OMB approval of the
proposed information collection. All
comments will become a matter of
public record.
Dated: June 9, 2020.
Virginia L. Mackay-Smith,
Associate Director.
BILLING CODE 4160–90–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60 Day-20–1161; Docket No. CDC–2020–
0068]
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 ‘‘Evaluation of Enhancing HIV
Prevention Communication and
Mobilization Efforts through Strategic
Partnerships.’’ This collection is
designed to assess the extent to which
partnership activities meet the
overarching goals for dissemination,
communication, and implementation of
national engagement efforts in support
of the U.S. Department of Health and
Human Services’ Ending the HIV
Epidemic.
jbell on DSKJLSW7X2PROD with NOTICES
VerDate Sep<11>2014
17:04 Jun 12, 2020
Jkt 250001
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:
404–639–7570; 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;
FOR FURTHER INFORMATION CONTACT:
[FR Doc. 2020–12804 Filed 6–12–20; 8:45 am]
SUMMARY:
CDC must receive written
comments on or before August 14, 2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2020–
0068 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.
DATES:
PO 00000
Frm 00022
Fmt 4703
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36205
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
Evaluation of Enhancing HIV
Prevention Communication and
Mobilization Efforts through Strategic
Partnerships (OMB Control No. 0920–
1161)—Reinstatement without Change—
National Center for HIV/AIDS, Viral
Hepatitis, STD and TB Prevention
(NCHHSTP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
To address the HIV epidemic in the
U.S., the Department of Health and
Human Services launched Ending the
HIV Epidemic: A Plan for America,
which is a cross-agency initiative
aiming to reduce new HIV infections in
the U.S. by 90% by 2030. CDC’s Let’s
Stop HIV Together campaign (formerly
known as Act Against AIDS) is part of
the national Ending the HIV Epidemic
initiative, and includes resources aimed
at reducing HIV stigma and promoting
testing, prevention, and treatment across
the HIV care continuum.
Within this context, CDC’s Division of
HIV/AIDS Prevention (DHAP) has and
will continue implementing various
partnership activities to increase HIV
awareness among the general public,
reduce new HIV infections among
disproportionately impacted
populations, and improve health
outcomes for people living with HIV/
AIDS in the US and its territories.
DHAP partners will be funded under
to (1) support the dissemination of
Together campaign materials,
messaging, and other CDC resources that
support HIV prevention and (2)
implement national engagement efforts
focusing on HIV prevention and
awareness. Partners represent civic/
social, media, and LGBT-focused
organizations. In addition, DHAP will
continue to engage and support the
private sector in promoting HIV
education, awareness, and policies in
the workplace. This may take the form
of encouraging businesses to implement
HIV/AIDS policies and education
programs in the workplace with the
overarching goal of increasing public
E:\FR\FM\15JNN1.SGM
15JNN1
Agencies
[Federal Register Volume 85, Number 115 (Monday, June 15, 2020)]
[Notices]
[Pages 36203-36205]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-12804]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Agency for Healthcare Research and Quality
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Agency for Healthcare Research and Quality, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces the intention of the Agency for
Healthcare Research and Quality (AHRQ) to request that the Office of
Management and Budget (OMB) approve the proposed information collection
project ``AHRQ Managing Unhealthy Alcohol Use in Primary Care
Initiative.'' This proposed information collection was previously
published in the Federal Register on March 30, 2020 and allowed 60 days
for public comment. AHRQ did not receive any comments during the
aforementioned public comment period. The purpose of this notice is to
allow an additional 30 days for public comment.
DATES: Comments on this notice must be received by 30 days after date
of publication of this notice.
ADDRESSES: Written 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.
FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427-1477, or by email at
[email protected].
SUPPLEMENTARY INFORMATION:
Proposed Project
AHRQ Managing Unhealthy Alcohol Use in Primary Care Initiative
The Affordable Care Act established the Patient-Centered Outcomes
Research Trust Fund (PCORTF) and authorized AHRQ to broadly disseminate
the research findings published by the Patient-Centered Outcomes
Research Institute (PCORI) and other government-funded research
relevant to comparative clinical effectiveness research. AHRQ's PCORTF-
funded initiative identifies research findings that could significantly
improve patient outcomes through broader implementation in clinical
practice. Under this initiative, in 2019 AHRQ launched a new
initiative, Managing Unhealthy Alcohol Use in Primary Care, in order to
promote the uptake of evidence-based practices for unhealthy alcohol
use (UAU). As part of this initiative, AHRQ selected six grantees and
funded a contractor to support and evaluate the grantees. The grantees
will collectively work with more than 700 primary care practices over
three years to implement and evaluate strategies to increase the use of
evidence-based interventions such as screening for unhealthy alcohol
use, brief interventions for adult patients who drink too much, and
medication-assisted therapy (MAT) for patients with an alcohol use
disorder. The contractor will develop a resource center, convene a
technical expert panel, conduct an ongoing environmental scan, support
a learning community of grantees, and complete a multisite, mixed
methods evaluation.
Unhealthy alcohol use, defined as behaviors ranging from risky
drinking to alcohol use disorders (AUD), is estimated to be the third
leading cause of preventable death in the United States. Between 2006
and 2010, nearly one in ten deaths were alcohol-related. In addition to
early mortality, UAU is associated with a host of adverse outcomes,
including unintentional injuries and the development or exacerbation of
a range of physical and behavioral health conditions. The Centers for
Disease Control and Prevention estimates suggest that excessive alcohol
consumption costs the United States $249 billion annually.
Under the UAU initiative, six AHRQ grantees will work to improve
the management of UAU in primary care by disseminating and implementing
evidence-based practices for screening and brief intervention, referral
to treatment (SBI/RT), and MAT in primary care practices. The multi-
site, mixed-methods evaluation will include primary data collection by
the evaluator,
[[Page 36204]]
NORC at the University of Chicago. The evaluation will also include
secondary data collected by the six grantee teams working with 750
primary care practices. Collectively the data will allow the evaluator
to assess the implementation and impact of the six grants.
The project goals, as laid out in the AHRQ request for applications
include:
Success of recruitment and retention strategies across all
six grantees to engage primary care practices for implementation of
SBI/RT and MAT, across the initiative;
Effectiveness of the grantees' collective dissemination
and implementation strategies, and the factors associated with the
success and/or failure of the strategies as it relates to populations,
settings and the influence of contextual factors;
Success at the practice level in increasing the number of
patients screened, identified, and treated; and
Overall impact on changes in processes or outcomes that
can be attributed to the initiative.
This study is being conducted pursuant to AHRQ's statutory
authority to broadly disseminate research findings published by the
Patient-Centered Outcomes Research Institute and other government-
funded research relevant to comparative clinical effectiveness research
to physicians, health care providers, and patients. 42 U.S.C 299b-37.
Method of Collection
To achieve the goals of the multi-site evaluation (MSE), AHRQ is
requesting OMB approval for three years for new data collection by the
evaluator. The evaluator's primary data collection is requested to
achieve the goals of the MSE and includes the following data collection
activities:
Semi-Structured Qualitative Interviews will take place in-person
and/or by telephone with key staff from each grantee team (i.e.,
principal investigator, co-investigator, evaluation lead, practice
facilitation/implementation lead, and project manager) and with
clinicians and staff at one primary care practice working with each
grantee. Interviews will be conducted annually beginning at the end of
Year 1, for a total of three time points per grantee. During Years 1
and 3 the interviews will be conducted by phone, while Year 2
interviews will be collected in-person. The interviews for both grantee
teams and primary care practice staff will cover domains such as
understanding the practice implementation and changes overtime, methods
of supporting practices, barriers and facilitators to implementation,
strategies to overcome barriers, and the number and type of staff
implementing SBI/RT and MAT.
Secondary data collected by grantees and analyzed by the evaluator
will include:
Aggregated process measure data that will be used to assess whether
the number of patients receiving SBI/RT and/or MAT increased at the
practice level. Grantees will survey all participating primary care
practices at the beginning of the initiative to collect data on basic
practice characteristics (e.g., size, ownership, staff, and patient
population) that can be used to evaluate relationships between practice
characteristics and the number of patients receiving SBI/RT and/or MAT.
Grantees will also collect quantitative information about the number,
duration, and function of contact between practice facilitators and
primary care practices to evaluate the relationship between duration,
frequency, and type of practice facilitator-practice engagement, and
the number of patients screened, receiving brief intervention, and/or
treated for UAU. The practice facilitators will collect data to track
changes in practices over time and facilitate an overall assessment of
what activities the practice is conducting to identify and manage UAU.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated annualized burden hours for the
respondents' time to complete the semi-structured Key Informant
Interviews. For the three-year clearance period, the estimated
annualized burden hours for the interviews are 60.
Exhibit 1
----------------------------------------------------------------------------------------------------------------
Number of
Data collection activity Number of responses per Hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Semi-Structured Interviews...................... 60 1 1.0 60
---------------------------------------------------------------
Total....................................... 60 .............. .............. 60
----------------------------------------------------------------------------------------------------------------
Exhibit 2 shows the estimated annualized cost burden based on the
respondents' time to complete the Key Informant Interviews. The total
annualized cost burden is estimated to be $6,109.
Exhibit 2--Estimated Annualized Cost Burden
----------------------------------------------------------------------------------------------------------------
Number of Total burden Average hourly Total cost
Form name respondents hours wage rate * burden
----------------------------------------------------------------------------------------------------------------
Semi-Structured Interviews...................... 60 60 \a\ $101.82 $6,109
---------------------------------------------------------------
Total....................................... 60 60 .............. 6,109
----------------------------------------------------------------------------------------------------------------
* National Compensation Survey: Occupational wages in the United States May 2018 ``U.S. Department of Labor,
Bureau of Labor Statistics'': https://www.bls.gov/oes/current/oes_stru.htm.
\a\ Based on the mean wages for 29-1062 Family and General Practitioners.
Request for Comments
In accordance with the Paperwork Reduction Act, comments on AHRQ's
information collection are requested with regard to any of the
following: (a) Whether the proposed collection of information is
necessary for the proper performance of AHRQ's health care research and
health care information
[[Page 36205]]
dissemination functions, including whether the information will have
practical utility; (b) the accuracy of AHRQ's estimate of burden
(including hours and costs) of the proposed collection(s) 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 upon the respondents, including the use
of automated collection techniques or other forms of information
technology.
Comments submitted in response to this notice will be summarized
and included in the Agency's subsequent request for OMB approval of the
proposed information collection. All comments will become a matter of
public record.
Dated: June 9, 2020.
Virginia L. Mackay-Smith,
Associate Director.
[FR Doc. 2020-12804 Filed 6-12-20; 8:45 am]
BILLING CODE 4160-90-P