Notice2024-19611
Agency Forms Undergoing Paperwork Reduction Act Review
Primary source
Metadata and text below are from the Federal Register, a public-domain U.S. government work. Always verify the official published version before relying on it for any legal matter.
Published
September 3, 2024
Issuing agencies
Health and Human Services DepartmentCenters for Disease Control and Prevention
Full Text
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<title>Federal Register, Volume 89 Issue 170 (Tuesday, September 3, 2024)</title>
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[Federal Register Volume 89, Number 170 (Tuesday, September 3, 2024)]
[Notices]
[Pages 71275-71276]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2024-19611]
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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 <a href="http://www.reginfo.gov/public/do/PRAMain">www.reginfo.gov/public/do/PRAMain</a>. 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
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Average
Number of Number of burden per
Type of respondents Form name respondents responses per response (in
respondent hours)
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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.
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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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