View Information Collection Request (ICR) Package
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Please note that the OMB number and expiration date may not have been determined when this Information Collection Request and associated Information Collection forms were submitted to OMB. The approved OMB number and expiration date may be found by clicking on the Notice of Action link below.
View ICR - OIRA Conclusion
OMB Control No:
0920-1092
ICR Reference No:
201902-0920-005
Status:
Historical Active
Previous ICR Reference No:
201507-0920-009
Agency/Subagency:
HHS/CDC
Agency Tracking No:
0920-1092
Title:
Sudden Death in the Young Registry
Type of Information Collection:
Reinstatement with change of a previously approved collection
Common Form ICR:
No
Type of Review Request:
Regular
OIRA Conclusion Action:
Approved without change
Conclusion Date:
04/09/2019
Retrieve Notice of Action (NOA)
Date Received in OIRA:
02/26/2019
Terms of Clearance:
Approved consistent with the understanding that CDC will not be conducting any general research on the information collected from SDY cases. When communicating findings from this collection, all publications will clearly describe the scope and limitations of the study findings. In addition, CDC should improve their monitoring of expiring information collections to avoid unnecessary reinstatement requests.
Inventory as of this Action
Requested
Previously Approved
Expiration Date
04/30/2022
36 Months From Approved
12/31/2018
Responses
2,576
0
10,800
Time Burden (Hours)
521
0
900
Cost Burden (Dollars)
17,538
0
0
Abstract:
The goal of the Sudden Death in the Young (SDY) Case Registry is to improve and standardize case ascertainment so funded jurisdictions can better their understanding of the incidence and risk factors for sudden death in youth. Data will be used to inform the descriptive epidemiology of SDY, including the incidence, and risk factors. These data will be used to inform prevention strategies as well as best practices for national surveillance of SDY. The changes proposed with this reinstatement include a decrease in burden due to more accurate estimates of time needed to complete modules and better estimates of the number of respondents and the number requiring advanced review.
Authorizing Statute(s):
PL:
Pub.L. 113 - 236 2
Name of Law: Sudden Unexpected Death Data Enhancement and Awareness Act
US Code:
42 USC 241
Name of Law: Public Health Service Act
Citations for New Statutory Requirements:
None
Associated Rulemaking Information
RIN:
Stage of Rulemaking:
Federal Register Citation:
Date:
Not associated with rulemaking
Federal Register Notices & Comments
60-day Notice:
Federal Register Citation:
Citation Date:
83 FR 55547
11/06/2018
30-day Notice:
Federal Register Citation:
Citation Date:
84 FR 5687
02/22/2019
Did the Agency receive public comments on this ICR?
No
Number of Information Collection (IC) in this ICR:
3
IC Title
Form No.
Form Name
Advanced Review
SDY Module - Epileptologists
NA
NCRPCD Case Reporting System - SDY Module
SDY Module - Forensic Pathologists
NA
NCRPCD Case Reporting System - SDY Module
SDY Module - Neurologists
NA
NCRPCD Case Reporting System - SDY Module
SDY Module - Pediatric Cardiologists
NA
NCRPCD Case Reporting System - SDY Module
SDY Module - State Health Personnel
none
NCFRP Cases Reporting System SDY Module 1
SDY Module N for State Health Personnel
none
NCFRP Case Reporting SDY Module N
ICR Summary of Burden
Total Approved
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
2,576
10,800
0
-8,224
0
0
Annual Time Burden (Hours)
521
900
0
-379
0
0
Annual Cost Burden (Dollars)
17,538
0
0
17,538
0
0
Burden increases because of Program Change due to Agency Discretion:
Yes
Burden Increase Due to:
Miscellaneous Actions
Burden decreases because of Program Change due to Agency Discretion:
Yes
Burden Reduction Due to:
Miscellaneous Actions
Short Statement:
This reinstatement with changes includes using better estimates of the number of expected respondents, better estimates of the time required to respond, and better estimates of the number of cases that require advanced review. Changes in the advance review process resulted in the removal of medical expert specific ICs. The burden has decreased from 900 annual hours to 521 and the number of respondents has been reduced from 10,800 to 2,576.
Annual Cost to Federal Government:
$106,441
Does this IC contain surveys, censuses, or employ statistical methods?
Yes
Part B of Supporting Statement
Does this ICR request any personally identifiable information (see
OMB Circular No. A-130
for an explanation of this term)? Please consult with your agency's privacy program when making this determination.
No
Does this ICR include a form that requires a Privacy Act Statement (see
5 U.S.C. §552a(e)(3)
)? Please consult with your agency's privacy program when making this determination.
No
Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]?
No
Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]?
No
Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)?
No
Is this ICR related to the Pandemic Response?
Uncollected
Agency Contact:
Shari Steinberg 404 639-4942 sxw2@cdc.gov
Common Form ICR:
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:
(a) It is necessary for the proper performance of agency functions;
(b) It avoids unnecessary duplication;
(c) It reduces burden on small entities;
(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;
(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;
(f) It indicates the retention periods for recordkeeping requirements;
(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:
(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;
(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.
(i) It uses effective and efficient statistical survey methodology (if applicable); and
(j) It makes appropriate use of information technology.
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.
Certification Date:
02/26/2019
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