Notice2022-15730
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
July 22, 2022
Issuing agencies
Health and Human Services DepartmentCenters for Disease Control and Prevention
Full Text
<html>
<head>
<title>Federal Register, Volume 87 Issue 140 (Friday, July 22, 2022)</title>
</head>
<body><pre>
[Federal Register Volume 87, Number 140 (Friday, July 22, 2022)]
[Notices]
[Pages 43858-43859]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2022-15730]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-22-22CL]
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 Population-based Surveillance of Outcomes,
Needs, and Well-being of Children and Adolescents with Congenital Heart
Defects 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
14, 2022 to obtain comments from the public and affected agencies. CDC
received five 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
Population-based Surveillance of Outcomes, Needs, and Well-being of
Children and Adolescents with Congenital Heart Defects--New--National
Center on Birth Defects and Developmental Disabilities (NCBDDD),
Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Congenital heart defects (CHD) are the most common type of
structural birth defects, affecting approximately one in 110 live-born
children. Due to advances in survival, there are approximately one
million children with CHD in the United States. With vast declines in
mortality from pediatric heart disease over the past 30 years, it is
vital to evaluate health, social, educational, and quality of life
outcomes beyond infancy and early childhood. However, existing U.S.
population-based data are lacking on these outcomes among those born
with CHD and the changes that may occur with time and age. U.S. data is
needed to provide insight into the public health questions that remain
for this population and to develop services and allocate resources to
improve long-term health and well-being.
For this project, we will use data from U.S. birth defect
surveillance systems, or population-based studies derived from them, to
identify a population-based sample of children and adolescents two to
17 years of age born with CHD. Parents and caregivers of these
individuals will serve as respondents for the CHSTRONG-KIDS survey. The
CHSTRONG-KIDS survey will be administered at three sites. One site will
be Atlanta, Georgia, where CDC
[[Page 43859]]
has managed and led the Metropolitan Atlanta Congenital Defects Program
(MADCP) since 1967 and has a history of collaboration with local
hospitals and the Georgia Department of Health. A competitive review
process is underway to select the two additional sites. All three sites
will then use state databases and online search engines to find current
addresses for parents and caregivers of children with CHD and mail
paper surveys to them.
Survey questions inquire about the child's cardiac and other
healthcare utilization,barriers to health care, quality of life, social
and educational outcomes, and transition of care from childhood to
adulthoodas well asneeds andexperiencesof thecaregivers. The
information collected from this population-based survey will be used to
inform current knowledge, allocate resources, develop services, and,
ultimately, improve long-term health of children and adolescents born
with CHD and their caregivers.
OMB approval is requested for three years. During this period, we
estimate receiving completed surveys from a total of 7,667 caregivers
of children and adolescents with CHD, which equates to 2,556
respondents per year. To generate sufficient sample size, accounting
for non-response, we intend to sample 100% of eligible CHD cases
identified through select birth defect surveillance systems. The survey
takes approximately 20 minutes to complete, and includes skip patterns
so that parents or caregivers are only asked age-relevant questions
about their child to minimize burden per response. CDC estimates an
annual total burden of 852 hours. Survey participation is voluntary and
there are no costs to participants other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Caregivers of individuals aged 2- Congenital Heart Survey 2,556 1 20/60
17 years with a congenital heart To Recognize Outcomes,
defect. Needs, and wellbeinG of
KIDS (CHSTRONG-KIDS).
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2022-15730 Filed 7-21-22; 8:45 am]
BILLING CODE 4163-18-P
</pre></body>
</html>Indexed from Federal Register on July 22, 2022.
This is legal information, not legal advice. Laws vary by jurisdiction and change frequently. Always verify current law with official sources and consult a licensed attorney in your jurisdiction for advice on your specific situation.