Agency Forms Undergoing Paperwork Reduction Act Review, 71275-71276 [2024-19611]

Download as PDF 71275 Federal Register / Vol. 89, No. 170 / Tuesday, September 3, 2024 / Notices • Request for Medical Records Form—Miners wishing to receive copies of their CWHSP chest x-rays and related files must fully complete, sign, and email this form to cwhsp@cdc.gov. The form can also be mailed or faxed using the address and fax listed on the form. It is estimated that five minutes is required for the coal miner to complete this form. There are no costs to respondents other than their time. ESTIMATED ANNUALIZED BURDEN HOURS Average burden per response (in hours) No. of responses per respondent Total burden hours Form name Coal mine operator ............................. Coal Mine Contractor .......................... Radiograph Facility Supervisor ........... Coal Miner .......................................... Coal Miner—Radiograph .................... B Reader Physician ............................ Qualified and Licensed Physician (NIOSH Approved Radiograph Facility). Physicians taking the B Reader Examination. Spirometry Facility Supervisor ............ Spirometry Facility Employee ............. Spirometry Technician ........................ Coal Miner—Spirometry ..................... Request for Medical Records ............. Pathologist .......................................... Pathologist .......................................... Pathologist .......................................... Next-of-kin for deceased miner .......... 2.10 ..................................................... 2.18 ..................................................... 2.11 ..................................................... 2.9 ....................................................... No form required ................................ 2.8 ....................................................... 2.8 ....................................................... 268 165 20 4,345 4,788 10 4,788 1 1 1 1 1 899 1 30/60 30/60 30/60 20/60 15/60 3/60 3/60 134 83 10 1,448 1,197 450 240 2.12 ..................................................... 110 1 10/60 18 2.14 ..................................................... 2.13 ..................................................... 2.15 ..................................................... No form required ................................ Request for Medical Records Form ... 2.19 ..................................................... Invoice—No standard form ................ Pathology Report—No standard form 2.6 ....................................................... 15 619 619 619 779 4 4 4 4 1 1 1 1 1 1 1 l 1 30/60 5/60 20/60 15/60 5/60 15/60 5/60 5/60 15/60 8 52 206 155 65 1 1 1 1 Total ............................................. ............................................................. ........................ ............................ .................... 4,070 Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Public Health Ethics and Regulations, Office of Science, Centers for Disease Control and Prevention. [FR Doc. 2024–19614 Filed 8–30–24; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day-24–23IE] Agency Forms Undergoing Paperwork Reduction Act Review tkelley on LAP7H3WLY3PROD with NOTICES2 No. of respondents Type of respondent In accordance with the Paperwork Reduction Act of 1995, the Centers for Disease Control and Prevention (CDC) has submitted the information collection request titled ‘‘Social and Economic Barriers to Receiving Optimal Services Along the Cancer Care Continuum’’ 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 September 26, 2023 to obtain comments from the public and affected agencies. CDC did not receive comments related to the previous notice. This notice VerDate Sep<11>2014 22:46 Aug 30, 2024 Jkt 262001 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. PO 00000 Frm 00026 Fmt 4703 Sfmt 4703 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 Social and Economic Barriers to Receiving Optimal Services Along the Cancer Care Continuum—New— National Center for Chronic Disease Prevention and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC). Background and Brief Description The purpose of this project is to: (1) examine and better understand social and economic barriers faced by colorectal, breast, and cervical cancer survivors and their caregivers at each stage of the Cancer Care Continuum (CCC); and (2) quantify the impact of U:\REGISTER\03SEN1.SGM 03SEN1 71276 Federal Register / Vol. 89, No. 170 / Tuesday, September 3, 2024 / Notices individual and compounded barriers on health outcomes along the CCC for survivors. CDC will use a mixed methods data collection and analysis approach. First, CDC will pull our sample from cancer registry data in California, North Carolina, and Texas based on inclusion criteria (received first cancer diagnosis of either breast, cervical or colorectal cancer in 2021; 21–75 years of age at time of diagnosis; are non-Hispanic Black/African American, non-Hispanic White, or Hispanic; alive at the time of data extraction/sample selection). Then, CDC will administer a Wave 1 (baseline) and Wave 2 (one-year follow-up) survey to cancer survivors, as well as a survey to their caregivers. Additionally, CDC will conduct interviews with selected survivors and caregivers as well as focus groups with representatives from patient/survivor advocacy organizations. CDC will incorporate cancer registry data into the quantitative data analysis, and triangulate findings from the quantitative and qualitative data collection efforts. Results will be used to inform efforts aimed at increasing access to cancer care services, reducing the burden of cancers and closing the disparities gap. CDC requests OMB approval for an estimated 1,681 annual burden hours. There are no costs to respondents other than their time to participate. ESTIMATED ANNUALIZED BURDEN HOURS Form name Wave 1 Survivor Survey Respondents ........... Wave 2 Survivor Survey Respondents ........... Survivor Interviewees ...................................... Caregiver Survey Respondents ...................... Caregiver Interviewees ................................... Patient Advocacy Group—Focus Group Participants. W1 Survey Instrument ................................... W2 Survey Instrument ................................... Survivor Interview Guide ................................ Caregiver Survey Instrument ......................... Caregiver Interview Guide ............................. Advocacy Representatives Focus Group Guide. Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Public Health Ethics and Regulations, Office of Science, Centers for Disease Control and Prevention. [FR Doc. 2024–19611 Filed 8–30–24; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [Docket No. CDC–2024–0063] Meeting of the Advisory Committee to the Director (ACD), Centers for Disease Control and Prevention Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). AGENCY: Notice of meeting and request for comment. ACTION: In accordance with the Federal Advisory Committee Act, the Centers for Disease Control and Prevention (CDC) announces the following meeting for the Advisory Committee to the Director, Centers for Disease Control and Prevention (ACD, CDC). This is a hybrid meeting, accessible both in person and virtually (webcast live via the World Wide Web). It is open to the public and limited only by the space available. tkelley on LAP7H3WLY3PROD with NOTICES2 SUMMARY: VerDate Sep<11>2014 22:46 Aug 30, 2024 Jkt 262001 The meeting will be held on October 22, 2024, from 9 a.m. to 3:30 p.m., EDT (times subject to change). The public may submit written comments from September 3, 2024 through October 7, 2024. ADDRESSES: Meeting address: CDC Roybal Campus, Building 19, Auditorium B3, 1600 Clifton Road NE, Atlanta, Georgia 30329–4027. Please note that the meeting location, the CDC Roybal Campus, is a federal facility and in-person access is limited to United States citizens unless prior authorizations, taking up to 30 to 60 days, have been made. Registration: You must register to attend this meeting in person. If you wish to attend in person, please submit a request by email to ACDirector@ cdc.gov at least 5 business days in advance of the meeting. No registration is required to view the meeting via the World Wide Web. Information for accessing the webcast will be available at https://www.cdc.gov/about/advisorycommittee-director/. Written comments: You may submit comments, identified by Docket No. CDC–2024–0063 by either of the following methods below. Do not submit comments for the docket by email. CDC does not accept comments for the docket by email. • Federal eRulemaking Portal: https://www.regulations.gov. Follow the instructions for submitting comments. • Mail: Demetria Gardner, BA, Centers for Disease Control and Prevention, 1600 Clifton Road NE, DATES: PO 00000 Frm 00027 Fmt 4703 Sfmt 4703 Number of responses per respondent Number of respondents Type of respondents 3,000 1,200 20 900 20 16 1 1 1 1 1 1 Average burden per response (in hours) 20/60 20/60 1 15/60 1 1 Mailstop H21–10, Atlanta, Georgia 30329–4027. Attn: Docket number CDC– 2024–0063. Instructions: All submissions received must include the Agency name and Docket Number. All relevant comments received in conformance with the https://www.regulations.gov, suitability policy will be posted without change to https://www.regulations.gov, including any personal information provided. For access to the docket to read background documents or comments received, go to https://www.regulations.gov. Written public comments submitted up to 72 hours prior to the ACD meeting will be provided to ACD members before the meeting. Written comments received in advance of the meeting will be included in the official record of the meeting. FOR FURTHER INFORMATION CONTACT: Demetria Gardner, BA, Office of the Chief of Staff, Centers for Disease Control and Prevention, 1600 Clifton Road NE, Mailstop H21–10, Atlanta, Georgia 30329–4027, Telephone: (770) 488–4745; Email Address: ACDirector@ cdc.gov. SUPPLEMENTARY INFORMATION: Purpose: The Advisory Committee to the Director, CDC, shall (1) make recommendations to the Director regarding ways to prioritize the activities of the agency in alignment with the CDC Strategic Plan required under section 305(c); H.R. 2617–1252; (2) advise on ways to achieve or improve performance metrics in relation to the CDC Strategic Plan, and other relevant metrics, as appropriate; (3) U:\REGISTER\03SEN1.SGM 03SEN1

Agencies

[Federal Register Volume 89, Number 170 (Tuesday, September 3, 2024)]
[Notices]
[Pages 71275-71276]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-19611]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30Day-24-23IE]


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 ``Social and Economic Barriers to Receiving 
Optimal Services Along the Cancer Care Continuum'' 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 September 26, 2023 to obtain comments from 
the public and affected agencies. CDC did not receive comments related 
to the previous notice. This notice serves to allow an additional 30 
days for public and affected agency comments.
    CDC will accept all comments for this proposed information 
collection project. The Office of Management and Budget is particularly 
interested in comments that:
    (a) Evaluate whether the proposed collection of information is 
necessary for the proper performance of the functions of the agency, 
including whether the information will have practical utility;
    (b) Evaluate the accuracy of the agencies estimate of the burden of 
the proposed collection of information, including the validity of the 
methodology and assumptions used;
    (c) Enhance the quality, utility, and clarity of the information to 
be collected;
    (d) Minimize the burden of the collection of information on those 
who are to respond, including, through the use of appropriate 
automated, electronic, mechanical, or other technological collection 
techniques or other forms of information technology, e.g., permitting 
electronic submission of responses; and
    (e) Assess information collection costs.
    To request additional information on the proposed project or to 
obtain a copy of the information collection plan and instruments, call 
(404) 639-7570. Comments and recommendations for the proposed 
information collection should be sent within 30 days of publication of 
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular 
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function. Direct 
written comments and/or suggestions regarding the items contained in 
this notice to the Attention: CDC Desk Officer, Office of Management 
and Budget, 725 17th Street NW, Washington, DC 20503 or by fax to (202) 
395-5806. Provide written comments within 30 days of notice 
publication.

Proposed Project

    Social and Economic Barriers to Receiving Optimal Services Along 
the Cancer Care Continuum--New--National Center for Chronic Disease 
Prevention and Health Promotion (NCCDPHP), Centers for Disease Control 
and Prevention (CDC).

Background and Brief Description

    The purpose of this project is to: (1) examine and better 
understand social and economic barriers faced by colorectal, breast, 
and cervical cancer survivors and their caregivers at each stage of the 
Cancer Care Continuum (CCC); and (2) quantify the impact of

[[Page 71276]]

individual and compounded barriers on health outcomes along the CCC for 
survivors. CDC will use a mixed methods data collection and analysis 
approach. First, CDC will pull our sample from cancer registry data in 
California, North Carolina, and Texas based on inclusion criteria 
(received first cancer diagnosis of either breast, cervical or 
colorectal cancer in 2021; 21-75 years of age at time of diagnosis; are 
non-Hispanic Black/African American, non-Hispanic White, or Hispanic; 
alive at the time of data extraction/sample selection). Then, CDC will 
administer a Wave 1 (baseline) and Wave 2 (one-year follow-up) survey 
to cancer survivors, as well as a survey to their caregivers. 
Additionally, CDC will conduct interviews with selected survivors and 
caregivers as well as focus groups with representatives from patient/
survivor advocacy organizations.
    CDC will incorporate cancer registry data into the quantitative 
data analysis, and triangulate findings from the quantitative and 
qualitative data collection efforts. Results will be used to inform 
efforts aimed at increasing access to cancer care services, reducing 
the burden of cancers and closing the disparities gap. CDC requests OMB 
approval for an estimated 1,681 annual burden hours. There are no costs 
to respondents other than their time to participate.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                                      Average
                                                                     Number of       Number of      burden per
          Type of respondents                   Form name           respondents    responses per   response  (in
                                                                                    respondent        hours)
----------------------------------------------------------------------------------------------------------------
Wave 1 Survivor Survey Respondents....  W1 Survey Instrument....           3,000               1           20/60
Wave 2 Survivor Survey Respondents....  W2 Survey Instrument....           1,200               1           20/60
Survivor Interviewees.................  Survivor Interview Guide              20               1               1
Caregiver Survey Respondents..........  Caregiver Survey                     900               1           15/60
                                         Instrument.
Caregiver Interviewees................  Caregiver Interview                   20               1               1
                                         Guide.
Patient Advocacy Group--Focus Group     Advocacy Representatives              16               1               1
 Participants.                           Focus Group Guide.
----------------------------------------------------------------------------------------------------------------


Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Public Health 
Ethics and Regulations, Office of Science, Centers for Disease Control 
and Prevention.
[FR Doc. 2024-19611 Filed 8-30-24; 8:45 am]
BILLING CODE 4163-18-P
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