Agency Information Collection Activities: Proposed Collection; Comment Request, 77588-77590 [2023-24872]

Download as PDF 77588 Federal Register / Vol. 88, No. 217 / Monday, November 13, 2023 / Notices Background On November 6, 2021, Congress passed the Bipartisan Infrastructure Law (BIL), also known as the Infrastructure Investment and Jobs Act (IIJA). On November 15, 2021, the President signed Executive Order (E.O.) 14052 ‘‘Implementation of the Infrastructure Investment and Jobs Act.’’ On December 13, 2021, the President signed E.O. 14508 ‘‘Transforming Federal Customer Experience and Service Delivery to Rebuild Trust in Government.’’ On February 25, 2022, President Biden and the GSA announced the list of major LPOE projects funded by the BIL. This included the Bridge of the Americas (BOTA) LPOE in El Paso, Texas. The Environmental Impact Statement (EIS) will be prepared in accordance with section 102 of the National Environmental Policy Act (NEPA) of 1969 (42 United States Code [U.S.C.] 4321 to 4370d), as implemented by the regulations promulgated by the Council on Environmental Quality (CEQ) (40 Code of Federal Regulations [CFR] 1500–1508). The principal objectives of NEPA are to ensure the careful consideration of environmental aspects of proposed actions in Federal decisionmaking processes and to make environmental information available to decision makers and the public before decisions are made and actions are taken. Additionally, this EIS will be prepared in accordance with GSA NEPA guidelines (GSA Order ADM 1095.1F and the Public Buildings Service [PBS] NEPA Desk Guide, both dated October 1999) and serves as a mechanism for compliance with the National Historic Preservation Act (NHPA) of 1966 (as amended) and other relevant laws and/ or regulations. Scoping Process khammond on DSKJM1Z7X2PROD with NOTICES The purpose of this initial public scoping meeting is to seek input from stakeholders and the public regarding potential environmental issues that could affect the proposed project. The EIS will include public input on alternatives being developed to implement the proposed improvements and the potential impacts that could result from implementing those improvements. Purpose and Need for Action The purpose of the proposed action is for the GSA to support the U.S. Customs and Border Protection (CBP) mission by bringing the BOTA LPOE infrastructure in line with current CBP land port design standards (i.e., CBP Land Port of Entry Design Standard) and operational VerDate Sep<11>2014 17:12 Nov 09, 2023 Jkt 262001 requirements while addressing existing deficiencies identified with the ongoing port operations. In order to bring the BOTA LPOE in line with CBP’s design standards and operational requirements, action is needed to satisfy the following overriding needs: • Improve the capacity and functionality of the LPOE to meet future public demand, while maintaining the capability to meet border security initiatives. • Ensure the safety and security for the employees and the travelling public. Proposed Action and Alternatives Development As part of initial project planning, the GSA has developed three (3) action alternatives as potential means of implementing the proposed action. The no action alternative will also be considered in the EIS. All three action alternatives include the phased razing of all existing buildings/structures and infrastructure within the existing LPOE boundaries and construction of new buildings/structures and supporting infrastructure. All three also include minimal land acquisition in areas immediately adjacent to the port. Summary of Potential Impacts The EIS will identify, describe, and analyze the potential effects of the action alternatives developed to implement the proposed action and the no action alternative. This will include direct, indirect, and cumulative effects. At present, GSA has identified the following resources/issues for analysis of both beneficial and adverse potential impacts: • Hazardous Materials, Waste, and/or Site Contamination • Socioeconomics (including Environmental Justice) • Public Services, Infrastructure, and Utilities • Surface Waters, Drainage, and Floodplains • Land Use and Zoning (including Visual and Aesthetics) • Traffic (Vehicular and Pedestrian), Transportation, and Parking • Air Quality (including Greenhouse Gas Emissions) • Noise and Vibration • Cultural and Historic Resources The EIS will document measures that could potentially avoid, minimize, or mitigate any identified adverse impacts. GSA welcomes public input on these potential impacts and other resources that could be considered. PO 00000 Frm 00040 Fmt 4703 Sfmt 4703 Anticipated Schedule for DecisionMaking Process All dates are estimated and may change. • EIS NOI published in the Federal Register: Friday November 17, 2023. • Initial NEPA Scoping Meeting: Wednesday December 13, 2023. • End of Initial NEPA Scoping Period: Tuesday January 16, 2024. • Publication of the Draft EIS: May– June 2024 TBD. • Draft EIS Public Comment Period: June–August 2024 TBD. • Final EIS: September 2024 TBD. • Record of Decision: October 2024 TBD. Michael Clardy, Director, Facilities Management Division. [FR Doc. 2023–24927 Filed 11–9–23; 8:45 am] BILLING CODE 6820–AY–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 ‘‘Questionnaire and Data Collection Testing, Evaluation, and Research for the Agency for Healthcare Research and Quality.’’ SUMMARY: Comments on this notice must be received by January 12, 2024. DATES: Written comments should be submitted to: Doris Lefkowitz, Reports Clearance Officer, AHRQ, by email at doris.lefkowitz@AHRQ.hhs.gov. Copies of the proposed collection plans, data collection instruments, and specific details on the estimated burden can be obtained from the AHRQ Reports Clearance Officer. ADDRESSES: FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ Reports Clearance Officer, (301) 427–1477, or by email at doris.lefkowitz@AHRQ.hhs.gov. SUPPLEMENTARY INFORMATION: E:\FR\FM\13NON1.SGM 13NON1 77589 Federal Register / Vol. 88, No. 217 / Monday, November 13, 2023 / Notices Proposed Project Questionnaire and Data Collection Testing, Evaluation, and Research for the Agency for Healthcare Research and Quality The Agency for Healthcare Research and Quality (AHRQ) requests that the Office of Management and Budget (OMB) re-approve generic pre-testing clearance 0935–0124 for three years to facilitate AHRQ’s efforts to (1) employ evaluation-type methods and techniques to improve AHRQ’s current data collection and estimation procedures, (2) develop new collections and procedures, including toolkits, and (3) revise existing collections and procedures. AHRQ believes that developing, testing, and evaluating data collection and estimation procedures using survey methods and other techniques in anticipation of agencysponsored studies can improve its information collection efforts and the products it develops and allow AHRQ to be more responsive to fast-changing developments in the healthcare research field. This clearance request is limited to research on data collection, toolkit development, and estimation procedures and reports and does not extend to the collection of data for public release or policy formation. The current Clearance (0935–0124) was granted on January 31, 2021, and expires on January 31, 2024. This generic clearance will allow AHRQ to draft and test toolkits, survey instruments and other data collection and estimation procedures more quickly and with greater lead time, thereby managing project time more efficiently and improving the quality of the data AHRQ collects. In some instances, the ability to test and evaluate toolkits, data collection and estimation procedures in anticipation of work or early in a project may result in the decision not to proceed with additional activities, thereby saving both public and private resources and effectively eliminating respondent burden. These preliminary research activities will not be used by AHRQ to regulate or sanction its customers. They will be entirely voluntary, and the confidentiality of respondents and their responses will be preserved. Proposed information collections submitted under this generic clearance will be submitted for review by OMB with a response expected in 14 days. Method of Collection The information collected through preliminary research activities under this generic clearance will be used by AHRQ to employ techniques to (1) improve AHRQ’s current data collection and estimation procedures, (2) develop new collections and procedures, including toolkits, and (3) revise existing collections and procedures in anticipation or in response to changes in the health or health care field. The end result will be improvement in AHRQ’s data collections and procedures, and the quality of data collected, a reduction or minimization of respondent burden, increased agency efficiency, and improved responsiveness to the public. Estimated Annual Respondent Burden Exhibit 1 shows the estimated burden hours, over the full three years of this clearance, for the respondents’ time to participate in the research activities that may be conducted under this generic clearance. Mail surveys will be conducted with about 6,000 persons (2,000 per year for three years) and are estimated to average 20 minutes. Mail surveys may also be sent to respondents via email and may include a telephone non-response follow-up. Telephone non-response follow-up for mailed surveys is not counted as a telephone survey in Exhibit 1. Not more than 600 persons, over three years, will participate in telephone surveys that will take about 40 minutes. Web-based surveys will be conducted with no more than 3,000 persons and will require no more than 10 minutes to complete. About 1,500 persons will participate in focus groups which may last up to two hours, while in-person interviews will be conducted with 600 persons and will take about 50 minutes. Automated data collection will be conducted for about 1,500 persons and could take up to 1 hour. Cognitive testing will be conducted with about 600 persons and is estimated to take 1.5 hours to complete. The total burden over three years is estimated to be 8,900 hours (about 2,967 hours per year). Exhibit 2 shows the estimated cost burden over three years, based on the respondents’ time to participate in these research activities. The total cost burden is estimated to be $412,028. EXHIBIT 1—ESTIMATED BURDEN HOURS OVER 3 YEARS Number of respondents Type of information collection Number of responses per respondent Hours per response Total burden hours Mail/email * ....................................................................................................... Telephone ........................................................................................................ Web-based ....................................................................................................... Focus Groups .................................................................................................. In-person .......................................................................................................... Automated ** .................................................................................................... Cognitive Testing *** ........................................................................................ 6,000 600 3,000 1,500 600 1,500 600 1 1 1 1 1 1 1 20/60 40/60 10/60 2.0 1.0 1.0 1.5 2,000 400 500 3,000 600 1,500 900 Totals ........................................................................................................ 13,800 na na 8,900 khammond on DSKJM1Z7X2PROD with NOTICES * May include telephone non-response follow-up in which case the burden will not change. ** May include testing of database software, CAPI software or other automated technologies. *** May include cognitive interviews for questionnaire or toolkit development, or ‘‘think aloud’’ testing of prototype websites. EXHIBIT 2—ESTIMATED COST BURDEN OVER 3 YEARS Number of respondents Type of information collection Mail/email ......................................................................................................... Telephone ........................................................................................................ Web-based ....................................................................................................... Focus Groups .................................................................................................. VerDate Sep<11>2014 17:12 Nov 09, 2023 Jkt 262001 PO 00000 Frm 00041 Fmt 4703 Sfmt 4703 Total burden hours 6,000 600 3,000 1,500 E:\FR\FM\13NON1.SGM 2,000 400 500 3,000 13NON1 Average hourly wage rate * $46.52 46.52 46.52 46.52 Total cost burden $93,040 18,608 23,260 139,560 77590 Federal Register / Vol. 88, No. 217 / Monday, November 13, 2023 / Notices EXHIBIT 2—ESTIMATED COST BURDEN OVER 3 YEARS—Continued Number of respondents Type of information collection Total burden hours Average hourly wage rate * Total cost burden In-person .......................................................................................................... Automated ........................................................................................................ Cognitive Testing ............................................................................................. 600 1,500 600 600 1,500 900 46.52 46.52 46.52 27,912 69,780 41,868 Totals ........................................................................................................ 13,800 8,900 na 412,028 * Bureau of Labor & Statistics on ‘‘Occupational Employment and Wages, May 2022’’ found at the following URL https://www.bls.gov/oes/current/oes_nat.htm#29-0000 for the respondents. Request for Comments In accordance with the Paperwork Reduction Act, 44 U.S.C. 3501–3520, 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 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: November 6, 2023. Marquita Cullom, Associate Director. [FR Doc. 2023–24872 Filed 11–9–23; 8:45 am] BILLING CODE 4160–90–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for Office of Management and Budget (OMB) Review; Information Comparison With Insurance Data Office of Child Support Services, Administration for Children and Families, Department of Health and Human Services. ACTION: Request for public comments. AGENCY: The Office of Child Support Services (OCSS), Administration for Children and Families (ACF), is requesting the OMB to extend approval of the Information Comparison with Insurance Data, with minor changes, for an additional three years. The current OMB approval (OMB No.: (0970–0342) expires January 31, 2024. 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/ SUMMARY: PRAMain. Find this particular information collection by selecting ‘‘Currently under 30-day Review—Open for Public Comments’’ or by using the search function. You can also obtain copies of the proposed collection of information by emailing infocollection@ acf.hhs.gov. Identify all emailed requests by the title of the information collection. SUPPLEMENTARY INFORMATION: Description: The Deficit Reduction Act of 2005 amended section 452 of the Social Security Act to authorize the Health and Human Services Secretary, through the Federal Parent Locator Service, to conduct comparisons of information concerning individuals owing past-due child support with information maintained by insurers (or their agents) concerning insurance claims, settlements, awards, and payments. On a daily basis, OCSS sends the results of the insurance data match in an ‘‘Insurance Match Response Record’’ to child support agencies, that use the insurance data matches to collect past-due support from the insurance proceeds. OCSS incorporated a separate burden calculation for respondents opting to electronically report quarterly. Respondents: Insurers or their agents, including the U.S. Department of Labor and state agencies administering workers’ compensation programs, and the Insurance Services Office. ANNUAL BURDEN ESTIMATES Total number of respondents khammond on DSKJM1Z7X2PROD with NOTICES Collection instrument Insurance Match File: Quarterly Reporting Electronically ............................... Insurance Match File: Monthly Reporting Electronically ................................. Insurance Match File: Weekly Reporting Electronically .................................. Insurance Match File: Daily Reporting Electronically ...................................... Match File: Daily Reporting Manually .............................................................. VerDate Sep<11>2014 17:12 Nov 09, 2023 Jkt 262001 PO 00000 Frm 00042 Fmt 4703 Sfmt 4703 Total number of responses per respondent 1 26 19 1 118 E:\FR\FM\13NON1.SGM 4 12 52 251 251 13NON1 Average burden hours per response 0.083 0.083 0.083 0.083 0.1 Total annual burden hours 0.33 25.90 82.00 20.83 2,961.80

Agencies

[Federal Register Volume 88, Number 217 (Monday, November 13, 2023)]
[Notices]
[Pages 77588-77590]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-24872]


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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 ``Questionnaire and Data Collection Testing, Evaluation, and 
Research for the Agency for Healthcare Research and Quality.''

DATES: Comments on this notice must be received by January 12, 2024.

ADDRESSES: Written comments should be submitted to: Doris Lefkowitz, 
Reports Clearance Officer, AHRQ, by email at 
[email protected].
    Copies of the proposed collection plans, data collection 
instruments, and specific details on the estimated burden can be 
obtained from the AHRQ Reports Clearance Officer.

FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ Reports 
Clearance Officer, (301) 427-1477, or by email at 
[email protected].

SUPPLEMENTARY INFORMATION: 

[[Page 77589]]

Proposed Project

Questionnaire and Data Collection Testing, Evaluation, and Research for 
the Agency for Healthcare Research and Quality

    The Agency for Healthcare Research and Quality (AHRQ) requests that 
the Office of Management and Budget (OMB) re-approve generic pre-
testing clearance 0935-0124 for three years to facilitate AHRQ's 
efforts to (1) employ evaluation-type methods and techniques to improve 
AHRQ's current data collection and estimation procedures, (2) develop 
new collections and procedures, including toolkits, and (3) revise 
existing collections and procedures. AHRQ believes that developing, 
testing, and evaluating data collection and estimation procedures using 
survey methods and other techniques in anticipation of agency-sponsored 
studies can improve its information collection efforts and the products 
it develops and allow AHRQ to be more responsive to fast-changing 
developments in the healthcare research field.
    This clearance request is limited to research on data collection, 
toolkit development, and estimation procedures and reports and does not 
extend to the collection of data for public release or policy 
formation. The current Clearance (0935-0124) was granted on January 31, 
2021, and expires on January 31, 2024.
    This generic clearance will allow AHRQ to draft and test toolkits, 
survey instruments and other data collection and estimation procedures 
more quickly and with greater lead time, thereby managing project time 
more efficiently and improving the quality of the data AHRQ collects. 
In some instances, the ability to test and evaluate toolkits, data 
collection and estimation procedures in anticipation of work or early 
in a project may result in the decision not to proceed with additional 
activities, thereby saving both public and private resources and 
effectively eliminating respondent burden.
    These preliminary research activities will not be used by AHRQ to 
regulate or sanction its customers. They will be entirely voluntary, 
and the confidentiality of respondents and their responses will be 
preserved. Proposed information collections submitted under this 
generic clearance will be submitted for review by OMB with a response 
expected in 14 days.

Method of Collection

    The information collected through preliminary research activities 
under this generic clearance will be used by AHRQ to employ techniques 
to (1) improve AHRQ's current data collection and estimation 
procedures, (2) develop new collections and procedures, including 
toolkits, and (3) revise existing collections and procedures in 
anticipation or in response to changes in the health or health care 
field. The end result will be improvement in AHRQ's data collections 
and procedures, and the quality of data collected, a reduction or 
minimization of respondent burden, increased agency efficiency, and 
improved responsiveness to the public.

Estimated Annual Respondent Burden

    Exhibit 1 shows the estimated burden hours, over the full three 
years of this clearance, for the respondents' time to participate in 
the research activities that may be conducted under this generic 
clearance. Mail surveys will be conducted with about 6,000 persons 
(2,000 per year for three years) and are estimated to average 20 
minutes. Mail surveys may also be sent to respondents via email and may 
include a telephone non-response follow-up. Telephone non-response 
follow-up for mailed surveys is not counted as a telephone survey in 
Exhibit 1. Not more than 600 persons, over three years, will 
participate in telephone surveys that will take about 40 minutes. Web-
based surveys will be conducted with no more than 3,000 persons and 
will require no more than 10 minutes to complete. About 1,500 persons 
will participate in focus groups which may last up to two hours, while 
in-person interviews will be conducted with 600 persons and will take 
about 50 minutes. Automated data collection will be conducted for about 
1,500 persons and could take up to 1 hour. Cognitive testing will be 
conducted with about 600 persons and is estimated to take 1.5 hours to 
complete. The total burden over three years is estimated to be 8,900 
hours (about 2,967 hours per year). Exhibit 2 shows the estimated cost 
burden over three years, based on the respondents' time to participate 
in these research activities. The total cost burden is estimated to be 
$412,028.

                                 Exhibit 1--Estimated Burden Hours Over 3 Years
----------------------------------------------------------------------------------------------------------------
                                                                     Number of
         Type of information collection              Number of     responses per     Hours per     Total burden
                                                    respondents     respondent       response          hours
----------------------------------------------------------------------------------------------------------------
Mail/email *....................................           6,000               1           20/60           2,000
Telephone.......................................             600               1           40/60             400
Web-based.......................................           3,000               1           10/60             500
Focus Groups....................................           1,500               1             2.0           3,000
In-person.......................................             600               1             1.0             600
Automated **....................................           1,500               1             1.0           1,500
Cognitive Testing ***...........................             600               1             1.5             900
                                                 ---------------------------------------------------------------
    Totals......................................          13,800              na              na           8,900
----------------------------------------------------------------------------------------------------------------
* May include telephone non-response follow-up in which case the burden will not change.
** May include testing of database software, CAPI software or other automated technologies.
*** May include cognitive interviews for questionnaire or toolkit development, or ``think aloud'' testing of
  prototype websites.


                                  Exhibit 2--Estimated Cost Burden Over 3 Years
----------------------------------------------------------------------------------------------------------------
                                                     Number of     Total burden   Average hourly    Total cost
         Type of information collection             respondents        hours        wage rate *       burden
----------------------------------------------------------------------------------------------------------------
Mail/email......................................           6,000           2,000          $46.52         $93,040
Telephone.......................................             600             400           46.52          18,608
Web-based.......................................           3,000             500           46.52          23,260
Focus Groups....................................           1,500           3,000           46.52         139,560

[[Page 77590]]

 
In-person.......................................             600             600           46.52          27,912
Automated.......................................           1,500           1,500           46.52          69,780
Cognitive Testing...............................             600             900           46.52          41,868
                                                 ---------------------------------------------------------------
    Totals......................................          13,800           8,900              na         412,028
----------------------------------------------------------------------------------------------------------------
* Bureau of Labor & Statistics on ``Occupational Employment and Wages, May 2022'' found at the following URL
  https://www.bls.gov/oes/current/oes_nat.htm#29-0000 for the respondents.

Request for Comments

    In accordance with the Paperwork Reduction Act, 44 U.S.C. 3501-
3520, 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 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: November 6, 2023.
Marquita Cullom,
Associate Director.
[FR Doc. 2023-24872 Filed 11-9-23; 8:45 am]
BILLING CODE 4160-90-P


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