Agency Forms Undergoing Paperwork Reduction Act Review, 51439-51441 [2020-18275]

Download as PDF 51439 Federal Register / Vol. 85, No. 162 / Thursday, August 20, 2020 / Notices of new HIV infections. In persons without HIV infection, ARVs can be given: (1) For 28 days following a potential HIV exposure through sexual or injection behaviors as nPEP, or (2) before potential sexual HIV exposures and taken daily for months to years as PrEP. In persons with HIV infection, beginning treatment with ARVs early in their infection (e.g., with high CD4 cell counts) can greatly lower their risk of transmitting infection to uninfected sexual partners; this is also called treatment as prevention or TasP. PrEP is 99% effective at reducing the risk of HIV through sexual contact when taken daily. PrEP is also 74%-84% effective at reducing the risk of HIV infection through injection drug use when taken daily. Persons living with HIV who are taking ARVs as prescribed, as well as achieving viral suppression, effectively have no risk for transmitting the virus to an HIV-negative partner through sexual contact. CDC is working with various jurisdictions with high HIV prevalence to increase capacity of ARV provision, build collaborative efforts between health departments and community-based organizations, and engage multi-sector provider systems to reach individuals with high risk of HIV infection as part of the End the HIV Epidemic Initiative. CBOs will play a crucial role in the End the HIV Epidemic Initiative. In a previous survey conducted by CDC’s Division of HIV/AIDS Prevention, CBOs reported high awareness of nPEP, PrEP, and TasP, but their ability to meet client need was low. Although clinical CBOs were more prepared to support the expansion of biomedical HIV prevention interventions, the likelihood that all CBOs would incorporate these interventions if they had additional resources was somewhat high. Research is needed to better understand the capacity of CBOs to incorporate biomedical HIV prevention interventions into their existing infrastructure. It is unclear whether the provision of and capacity to provide nPEP, PrEP, and TasP has increased among CBOs since the original survey was conducted. Furthermore, it is unclear whether non-clinical CBOs have achieved parity in linking clients to biomedical HIV prevention interventions with their clinical counterparts. This new survey will assess current capacity and provision of nPEP, PrEP, and TasP among CBOs providing HIV services to populations with increased risk for HIV acquisition. In addition, the results of this survey will be compared to the results of the 2015 survey to assess differences in awareness, capacity, and provision of biomedical HIV prevention interventions. Respondents will include organizations engaged in HIV prevention and outreach. Up to 330 respondents (n=330; 175 funded CBOs and 155 CBOs that did not receive funding) will be recruited to complete the survey. This project will employ a cross-sectional survey design. Executive level staff members of all CBOs within each of the two strata (mentioned above) will receive phone calls, using publicly available information, to elicit interest in participating in the survey. If the executive level staff member is not interested or is unable to complete the survey, he or she may nominate a direct client service provider and provide this person’s email address to study staff. Potential respondents will be contacted from a list of CBOs that completed the 2015 survey. Potential respondents from CBOs that received DHAP funding through PS15–1502 and PS17–1704 will also be contacted to determine their interest in participating in the data collection effort. Each organization’s representative will be sent an email with a link to the survey website (created with Survey Monkey). One link will be used for CBOs directly funded by CDC and a separate link will be used for unfunded CBOs. The email will instruct the recipient on how to complete the survey. Three email reminders will be sent to organizations for those that do not complete the survey. Email reminders will be sent two weeks, one month, and two months after the initial email if the potential respondent does not compete the survey. The survey should take approximately 30 minutes to complete. Where possible, data from the 2015 survey will be combined with data from the 2020 survey. Analyses will include completeness (non-response rates per item) as well as frequency of item responses for awareness, intentions, and provision of PrEP, nPEP, and TasP will be assessed for all respondents combined. Frequency and differences in item responses will be analyzed for relationship to CBO characteristics (e.g., clinical CBOs vs non-clinical CBOs). Frequency and differences in item responses will be analyzed across survey years. We will perform multivariable analysis as needed (to assess interactions between time and type of CBO). The total annualized burden hours is 165 hours. There are no other costs to respondents other than their time. ESTIMATED ANNUALIZED BURDEN HOURS Form name ......................................................................... Community Based Organization HIV Prevention Needs Assessment Survey. Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Scientific Integrity, Office of Science, Centers for Disease Control and Prevention. jbell on DSKJLSW7X2PROD with NOTICES Number of respondents Type of respondents DEPARTMENT OF HEALTH AND HUMAN SERVICES [FR Doc. 2020–18276 Filed 8–19–20; 8:45 am] Centers for Disease Control and Prevention BILLING CODE 4163–18–P [30Day–20–20HO] Agency Forms Undergoing Paperwork Reduction Act Review In accordance with the Paperwork Reduction Act of 1995, the Centers for Disease Control and Prevention (CDC) VerDate Sep<11>2014 18:01 Aug 19, 2020 Jkt 250001 PO 00000 Frm 00037 Fmt 4703 Sfmt 4703 330 Number of responses per respondent 1 Average burden per response (in hours) 30/60 has submitted the information collection request titled Heat-related Changes in Cognitive Performance 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 February 25, 2020 to obtain comments from the public and affected agencies. CDC did not receive comments related to the previous notice. This E:\FR\FM\20AUN1.SGM 20AUN1 51440 Federal Register / Vol. 85, No. 162 / Thursday, August 20, 2020 / Notices 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. jbell on DSKJLSW7X2PROD with NOTICES Proposed Project Heat-related Changes in Cognitive Performance—New—National Institute for Occupational Safety and Health (NIOSH), Centers for Disease Control and Prevention (CDC). Background and Brief Description NIOSH, under Public Law 91–173 as amended by Public Law 95 –164 (Federal Mine Safety and Health Act of 1977), and Public Law 109–236 (Mine Improvement and New Emergency Response Act of 2006) has the VerDate Sep<11>2014 18:01 Aug 19, 2020 Jkt 250001 responsibility to conduct research to improve working conditions and to prevent accidents and occupational diseases in U.S. mines. Heat strain is one of these occupational diseases and is an increasing problem among many industries, including mining. As mines expand into deeper and hotter environments, and as heat waves occur with increasing frequency and severity, heat strain among underground and surface miners is likely to increase. Not only can heat strain lead to heat illness, but studies have demonstrated associations between heat exposure and work injuries. Although the underlying mechanism between heat exposure and injury is not known, reduced cognitive function is likely contributory. Despite the increasing importance of heat strain in mining, few studies have focused on heat strain among U.S. miners. The few studies that are available have demonstrated that miners often exceed a core body temperature of 38 °C during work activities, which is above the recommended threshold, but more information on frequency, duration, and intensity of elevated core body temperatures is needed in order to focus future heat strain research to better serve the mining industry. In addition to determining the patterns of duration and intensity of heat strain among U.S. miners, investigating the additional effects of heat strain beyond the risk of heat illness is an important step in improving miner health and safety. Studies have demonstrated associations between heat stress and cognitive deficits, but substantial inter- and intraindividual variability exists in the physiologic and cognitive responses to heat exposure. More information is needed about the most important factors (e.g., age, sex, chronic disease, fitness level, hydration) contributing to individual variability as well as interactions between these factors, because individual variability likely affects the usefulness of one-size-fits-all heat stress indices that are currently used in mining. Additionally, it is unclear which characteristics of core body temperature (e.g., absolute temperature thresholds vs. rising or falling temperatures vs rate of temperature change) are most associated with cognitive dysfunction. A better understanding of how individual variability and core body temperature relate to cognitive deficits would assist in developing strategies for screening and monitoring miners to mitigate or prevent heat strain. Therefore, this study aims to assess the following objectives: (1) Whether a core body temperature threshold exists at which PO 00000 Frm 00038 Fmt 4703 Sfmt 4703 cognitive performance begins to decline, (2) What factors most contribute to individual variability in cognitive and physiologic responses to heat, and (3) What patterns of duration and intensity of heat strain are most common among U.S. surface and underground miners. To study these objectives, a dual-arm field and laboratory study will be conducted. The field study will be conducted at surface and underground mines. Data will be collected from miners working in warm or hot areas of participating mines. Participants will swallow temperature pills to measure core body temperature and will wear bio-harnesses to measure heart rate. Two six-minute assessments will be taken during each shift. The assessments include questions on sleepiness and work tasks and a Psychomotor Vigilance Test (PVT) to assess vigilant attention and reaction time. An initial screening questionnaire as well as post-shift questionnaires will be used to obtain information on risk factors for heat strain and cognitive deficits. The purpose of collecting data at the field sites is to evaluate the frequency, duration, and intensity of heat strain by monitoring core body temperature and heart rate throughout two complete shifts, as well as to assess associations between core body temperature and cognitive deficits. The laboratory study will be conducted in an environmental chamber, in which environmental conditions can be highly controlled. Data will be collected from miners, construction workers, and firefighters. These three groups were chosen because of their risk of heat exposure and their proximity to the NIOSH laboratory where the study will be conducted. Participants will perform alternating resistance and aerobic exercises followed by brief surveys to evaluate sleepiness (Karolinska Sleepiness Scale), affect (Positive and Negative Affect Schedule), and fatigue. Following these surveys, two cognitive tests (PVT and N-back, which measures vigilance, working memory, and complex tracking) will be administered. Testing will occur at room temperature and in hot conditions to compare cognitive test results between conditions. Participants will swallow temperature pills and wear bio-harnesses to enable the collection of real-time core body temperature and heart rate data. An initial health screening questionnaire as well as additional questionnaires administered prior to each test will be used to ensure that participants are able to withstand the physical demands of testing and to provide information on factors that affect individual variability to heat E:\FR\FM\20AUN1.SGM 20AUN1 51441 Federal Register / Vol. 85, No. 162 / Thursday, August 20, 2020 / Notices tolerance. Additionally, a physical examination and fingerstick blood tests will be used for health screening. The purpose of collecting data in the environmental chamber is to compare physiologic and cognitive measurements at different core body temperatures to evaluate factors contributing to individual variability in cognitive and physiologic responses to heat and to evaluate whether core body temperature thresholds exist above which cognitive deficits are observed. The total estimated burden hours are 103. There are no costs to respondents other than their time. ESTIMATED ANNUALIZED BURDEN HOURS Type of respondent Number responses per respondent Number of respondents Form name Average burden per response (hours) Miners. Ingestion of temperature pill ................................................... Fitting of chest strap ............................................................... Consent form (field) ................................................................ Health screening questionnaire (field) ................................... Heat stress app—shift questionnaire (field) ........................... PVT cognitive test (field) ........................................................ Heat stress app—post—shift questionnaire (field) ................ Ingestion of temperature pill ................................................... Fitting of chest strap ............................................................... Consent form (chamber) ........................................................ Physical .................................................................................. examination ............................................................................ Health screening questionnaire (chamber) ............................ 30 30 30 30 30 30 30 15 15 15 15 2 2 1 1 4 5 2 3 3 1 1 1/60 1/60 30/60 30/60 1/60 5/60 10/60 1/60 1/60 30/60 10/60 15 1 30/60 Fingerstick blood sample for point-of-care testing ................. Release of .............................................................................. Information (HIPPA) ............................................................... Borg and thermal scale .......................................................... PANAS KSS fatigue ............................................................... Cognitive test: PVT (chamber) ............................................... Cognitive test: N-back ............................................................ Pre-test screening questionnaire (chamber) .......................... 8 3 1 1 1/60 1/60 15 15 15 15 15 5 5 5 5 2 1/60 2/60 10/60 1/60 5/60 Miners/ .................................... firefighters/ .............................. construction workers. Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Scientific Integrity, Office of Science, Centers for Disease Control and Prevention. [FR Doc. 2020–18275 Filed 8–19–20; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Administration for Native Americans (ANA) Ongoing Progress Report (OPR) and Objective Work Plan (OWP) Administration for Native Americans, Administration for Children and Families, HHS. ACTION: Request for public comment. AGENCY: The Administration for Children and Families’ (ACF) Administration for Native Americans (ANA) is requesting a revision to the information collection: Ongoing Progress Report (OPR) and the Objective Work Plan (OWP) (OMB #0970–0452). Changes are proposed to reduce the jbell on DSKJLSW7X2PROD with NOTICES SUMMARY: VerDate Sep<11>2014 18:01 Aug 19, 2020 Jkt 250001 burden on the public by combining ANA’s Annual Data Report (OMB #0970–0475) with the OPR. DATES: Comments due within 30 days of publication. OMB must make a decision about the collection of information between 30 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. 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. SUPPLEMENTARY INFORMATION: Description: Content changes are being made to the currently approved OPR. ANA will continue to use the currently approved OPR with minimal changes to the instructions for the remainder of fiscal year (FY) 2020 and will use the modified OPR beginning FY 2021. The PO 00000 Frm 00039 Fmt 4703 Sfmt 4703 modified OPR combines ANA’s Annual Data Report (OMB #0970–0475) with the OPR. The information in the OPR is collected on a semi-annual basis to monitor the performance of grantees and better gauge grantee progress. The semiannual data collection replaces the previous quarterly filing requirement of the OPR. The OPR information collection is conducted in accordance with Sec. 811 [42 U.S.C. 2992] of the Native American Programs Act and will allow ANA to report quantifiable results across all program areas. It also provides grantees with parameters for reporting their progress and helps ANA better monitor and determine the effectiveness of their projects. There are no changes proposed to the OWP. The OWP information collection is conducted in accordance with 42 U.S.C. of the Native American Programs Act of 1972, as amended. This collection is necessary to evaluate applications for financial assistance and determine the relative merits of the projects for which such assistance is E:\FR\FM\20AUN1.SGM 20AUN1

Agencies

[Federal Register Volume 85, Number 162 (Thursday, August 20, 2020)]
[Notices]
[Pages 51439-51441]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-18275]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30Day-20-20HO]


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 Heat-related Changes in Cognitive Performance 
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 February 25, 2020 to 
obtain comments from the public and affected agencies. CDC did not 
receive comments related to the previous notice. This

[[Page 51440]]

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

    Heat-related Changes in Cognitive Performance--New--National 
Institute for Occupational Safety and Health (NIOSH), Centers for 
Disease Control and Prevention (CDC).

Background and Brief Description

    NIOSH, under Public Law 91-173 as amended by Public Law 95 -164 
(Federal Mine Safety and Health Act of 1977), and Public Law 109-236 
(Mine Improvement and New Emergency Response Act of 2006) has the 
responsibility to conduct research to improve working conditions and to 
prevent accidents and occupational diseases in U.S. mines. Heat strain 
is one of these occupational diseases and is an increasing problem 
among many industries, including mining. As mines expand into deeper 
and hotter environments, and as heat waves occur with increasing 
frequency and severity, heat strain among underground and surface 
miners is likely to increase. Not only can heat strain lead to heat 
illness, but studies have demonstrated associations between heat 
exposure and work injuries. Although the underlying mechanism between 
heat exposure and injury is not known, reduced cognitive function is 
likely contributory.
    Despite the increasing importance of heat strain in mining, few 
studies have focused on heat strain among U.S. miners. The few studies 
that are available have demonstrated that miners often exceed a core 
body temperature of 38 [deg]C during work activities, which is above 
the recommended threshold, but more information on frequency, duration, 
and intensity of elevated core body temperatures is needed in order to 
focus future heat strain research to better serve the mining industry.
    In addition to determining the patterns of duration and intensity 
of heat strain among U.S. miners, investigating the additional effects 
of heat strain beyond the risk of heat illness is an important step in 
improving miner health and safety. Studies have demonstrated 
associations between heat stress and cognitive deficits, but 
substantial inter- and intra-individual variability exists in the 
physiologic and cognitive responses to heat exposure. More information 
is needed about the most important factors (e.g., age, sex, chronic 
disease, fitness level, hydration) contributing to individual 
variability as well as interactions between these factors, because 
individual variability likely affects the usefulness of one-size-fits-
all heat stress indices that are currently used in mining. 
Additionally, it is unclear which characteristics of core body 
temperature (e.g., absolute temperature thresholds vs. rising or 
falling temperatures vs rate of temperature change) are most associated 
with cognitive dysfunction. A better understanding of how individual 
variability and core body temperature relate to cognitive deficits 
would assist in developing strategies for screening and monitoring 
miners to mitigate or prevent heat strain. Therefore, this study aims 
to assess the following objectives: (1) Whether a core body temperature 
threshold exists at which cognitive performance begins to decline, (2) 
What factors most contribute to individual variability in cognitive and 
physiologic responses to heat, and (3) What patterns of duration and 
intensity of heat strain are most common among U.S. surface and 
underground miners.
    To study these objectives, a dual-arm field and laboratory study 
will be conducted. The field study will be conducted at surface and 
underground mines. Data will be collected from miners working in warm 
or hot areas of participating mines. Participants will swallow 
temperature pills to measure core body temperature and will wear bio-
harnesses to measure heart rate. Two six-minute assessments will be 
taken during each shift. The assessments include questions on 
sleepiness and work tasks and a Psychomotor Vigilance Test (PVT) to 
assess vigilant attention and reaction time. An initial screening 
questionnaire as well as post-shift questionnaires will be used to 
obtain information on risk factors for heat strain and cognitive 
deficits. The purpose of collecting data at the field sites is to 
evaluate the frequency, duration, and intensity of heat strain by 
monitoring core body temperature and heart rate throughout two complete 
shifts, as well as to assess associations between core body temperature 
and cognitive deficits.
    The laboratory study will be conducted in an environmental chamber, 
in which environmental conditions can be highly controlled. Data will 
be collected from miners, construction workers, and firefighters. These 
three groups were chosen because of their risk of heat exposure and 
their proximity to the NIOSH laboratory where the study will be 
conducted. Participants will perform alternating resistance and aerobic 
exercises followed by brief surveys to evaluate sleepiness (Karolinska 
Sleepiness Scale), affect (Positive and Negative Affect Schedule), and 
fatigue. Following these surveys, two cognitive tests (PVT and N-back, 
which measures vigilance, working memory, and complex tracking) will be 
administered. Testing will occur at room temperature and in hot 
conditions to compare cognitive test results between conditions. 
Participants will swallow temperature pills and wear bio-harnesses to 
enable the collection of real-time core body temperature and heart rate 
data. An initial health screening questionnaire as well as additional 
questionnaires administered prior to each test will be used to ensure 
that participants are able to withstand the physical demands of testing 
and to provide information on factors that affect individual 
variability to heat

[[Page 51441]]

tolerance. Additionally, a physical examination and fingerstick blood 
tests will be used for health screening. The purpose of collecting data 
in the environmental chamber is to compare physiologic and cognitive 
measurements at different core body temperatures to evaluate factors 
contributing to individual variability in cognitive and physiologic 
responses to heat and to evaluate whether core body temperature 
thresholds exist above which cognitive deficits are observed.
    The total estimated burden hours are 103. There are no 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        (hours)
----------------------------------------------------------------------------------------------------------------
Miners.............................
                                     Ingestion of temperature                 30               2            1/60
                                      pill.
                                     Fitting of chest strap.....              30               2            1/60
                                     Consent form (field).......              30               1           30/60
                                     Health screening                         30               1           30/60
                                      questionnaire (field).
                                     Heat stress app--shift                   30               4            1/60
                                      questionnaire (field).
                                     PVT cognitive test (field).              30               5            5/60
                                     Heat stress app--post--                  30               2           10/60
                                      shift questionnaire
                                      (field).
                                     Ingestion of temperature                 15               3            1/60
                                      pill.
                                     Fitting of chest strap.....              15               3            1/60
                                     Consent form (chamber).....              15               1           30/60
                                     Physical...................              15               1           10/60
                                     examination................
                                     Health screening                         15               1           30/60
                                      questionnaire (chamber).
Miners/............................
firefighters/......................
construction workers...............
                                     Fingerstick blood sample                  8               1            1/60
                                      for point-of-care testing.
                                     Release of.................               3               1            1/60
                                     Information (HIPPA)........
                                     Borg and thermal scale.....              15               5            1/60
                                     PANAS KSS fatigue..........              15               5            2/60
                                     Cognitive test: PVT                      15               5           10/60
                                      (chamber).
                                     Cognitive test: N-back.....              15               5            1/60
                                     Pre-test screening                       15               2            5/60
                                      questionnaire (chamber).
----------------------------------------------------------------------------------------------------------------


Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific 
Integrity, Office of Science, Centers for Disease Control and 
Prevention.
[FR Doc. 2020-18275 Filed 8-19-20; 8:45 am]
BILLING CODE 4163-18-P
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