[NCBDDD] Population-based Surveillance of Outcomes, Needs, and Well-being of Children and Adolescents with Congenital Heart Defects

ICR 202310-0920-008

OMB: 0920-1382

Federal Form Document

Forms and Documents
Document
Name
Status
Form and Instruction
 Modified
Justification for No Material/Nonsubstantive Change
2023-10-18
Supplementary Document
2023-05-25
Supplementary Document
2023-05-25
Supplementary Document
2023-05-25
Supplementary Document
2023-05-25
Supplementary Document
2023-05-25
Supplementary Document
2023-05-25
Supplementary Document
2023-05-25
Justification for No Material/Nonsubstantive Change
2023-05-25
Supplementary Document
2022-11-23
Supplementary Document
2023-05-25
Supplementary Document
2023-05-25
Supplementary Document
2022-07-21
Supplementary Document
2023-05-25
Supplementary Document
2023-05-25
Supplementary Document
2022-07-21
Supplementary Document
2023-05-25
Supplementary Document
2023-05-25
Supplementary Document
2022-07-21
Supplementary Document
2022-07-21
Supplementary Document
2022-07-21
Supplementary Document
2023-05-25
Supplementary Document
2022-07-21
Supplementary Document
2022-07-21
Supporting Statement B
2022-11-23
Supporting Statement A
2022-11-23
IC Document Collections
IC ID
Document
Title
Status
254790 Modified
ICR Details
0920-1382 202310-0920-008
Received in OIRA 202305-0920-011
HHS/CDC 0920-1382-24AG
[NCBDDD] Population-based Surveillance of Outcomes, Needs, and Well-being of Children and Adolescents with Congenital Heart Defects
No material or nonsubstantive change to a currently approved collection   No
Regular 10/19/2023
  Requested Previously Approved
01/31/2026 01/31/2026
2,556 2,556
852 852
17,184 17,184
Data from U.S. state birth defect surveillance systems, or population-based studies derived from them, will be used to identify a population-based sample of children and adolescents 2 to 17 years of age born with congenital heart defects (CHD). Surveys will be mailed to their caregivers inquiring 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 adulthood as well as the needs and experiences of caregivers. Collected information will be used to inform current knowledge, allocate resources, develop services, and, ultimately, improve long-term health of children and adolescents born with CHD. In May 2023 CDC requested minor changes to improve survey accessibility and usability. These changes included edits to question wording; an online response option; and a telephone response option.
US Code: 42 USC 241, 247b-4 and 280g-13 Name of Law: Public Health Service Act
  
None
Not associated with rulemaking
  87 FR 8252 02/14/2022
87 FR 43858 07/22/2022
Yes
  Total Request Previously Approved Change Due to New Statute Change Due to Agency Discretion Change Due to Adjustment in Estimate Change Due to Potential Violation of the PRA
Annual Number of Responses 2,556 2,556 0 0 0 0
Annual Time Burden (Hours) 852 852 0 0 0 0
Annual Cost Burden (Dollars) 17,184 17,184 0 0 0 0
No
No
$773,031
Yes Part B of Supporting Statement
    Yes
    No
No
No
No
No
Thelma Sims 4046394771
  No
On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
 
 
 
 
 
 
 
    (i) Why the information is being collected;
    (ii) Use of information;
    (iii) Burden estimate;
    (iv) Nature of response (voluntary, required for a benefit, or mandatory);
    (v) Nature and extent of confidentiality; and
    (vi) Need to display currently valid OMB control number;
 
 
 
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.
10/19/2023
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