Generic Clearance to Support the Safe to Sleep Campaign at the Eunice Kennedy Shriver National Institute for Child Health and Human Development (NICHD)

Forms and Documents

Document Name	Status
pub 30 day FRN 2021-03870.pdf Supplementary Document	2021-02-25
0925-0701_NICHD_Safe to Sleep 2021_Substudy Submission Template (2).docx Supplementary Document	2021-02-12
0925-0701_NICHD_Safe to Sleep 2021_SSA.rev2.11.21.docx Supporting Statement A	2021-02-12

IC Document Collections

IC ID	Document Title	Status

ICR Details

OMB Control No: 0925-0701	ICR Reference No: 202102-0925-003
Status: Received in OIRA	Previous ICR Reference No: 201710-0925-003
Agency/Subagency: HHS/NIH	Agency Tracking No:
Title: Generic Clearance to Support the Safe to Sleep Campaign at the Eunice Kennedy Shriver National Institute for Child Health and Human Development (NICHD)
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular	Date Submitted to OIRA: 02/25/2021

	Requested	Previously Approved
Expiration Date	36 Months From Approved	02/28/2021
Responses	147,915	49,170
Time Burden (Hours)	39,915	12,920
Cost Burden (Dollars)	0	0

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Abstract: A revision for the Generic Clearance to Support the STS Campaign at the NICHD will allow campaign staff to gather feedback on campaign strategies and messages expeditiously and effectively, be better able to monitor and improve campaign implementation, and assess the utilization and practice activities of target audiences. The STS campaign generic clearance will fill a need that exists at NICHD to assess STS activities, particularly the continuing education program for nurses, new/revised campaign messages, Web development(i.e. website content, social media messages, videos, etc.), and materials (i.e. brochures, fact sheets, conversation guides, etc.) development.

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Authorizing Statute(s): US Code: 42 USC 285 Name of Law: The Public Health Service Act
  

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	85 FR 80123	12/11/2020
30-day Notice:	Federal Register Citation:	Citation Date:
	86 FR 11547	02/25/2021
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 0

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ICR Summary of Burden

	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	147,915	49,170	0	98,745	0	0
Annual Time Burden (Hours)	39,915	12,920	0	26,995	0	0
Annual Cost Burden (Dollars)	0	0	0	0	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: No

Burden Reduction Due to:

Short Statement: This is for three years vice the annualized burden that was previously submitted incorrectly.

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Annual Cost to Federal Government: $43,657

Does this IC contain surveys, censuses, or employ statistical methods? No

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.     Yes

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? No

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Common Form ICR:  No

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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: 02/25/2021

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