Generic Clearance for the Research Domain Criteria (RDoC) Initiative (NIMH)

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
pub 30day FRN2021-14630.pdf	Supplementary Document	Uploaded 2021-07-12	Repair queued
RDoC.Attachment 4 - HHS PIA - NIH NIMH Internet and Intranet Web Sites_2018.docx	Supplementary Document	Uploaded 2021-07-12	Repair queued
RDoC.Attachment 3- HHS PIA - NIH NIMH Headquarters Network System_2018.docx	Supplementary Document	Uploaded 2021-07-12	Repair queued
Attachment 2 Mini Supporting Statement Template.docx	Supplementary Document	Uploaded 2021-07-12	Repair queued
Attachment 1 - Previously Approved Studies under OMB # 0925-0756_062321_To Submit.docx	Supplementary Document	Uploaded 2021-07-12	Missing upstream
final SSA_NIMH RDoC Initiative Generic Clearance (OMB 0925-0756).docx	Supporting Statement A	Uploaded 2021-07-12	Repair queued

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form

ICR Details

OMB Control No: 0925-0756	ICR Reference No: 202107-0925-001
Status: Received in OIRA	Previous ICR Reference No: 201804-0925-001
Agency/Subagency: HHS/NIH	Agency Tracking No:
Title: Generic Clearance for the Research Domain Criteria (RDoC) Initiative (NIMH)
Type of Information Collection: Extension without change of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular	Date Submitted to OIRA: 07/13/2021

table that charts list comparision

	Requested	Previously Approved
Expiration Date	36 Months From Approved	07/31/2021
Responses	270	270
Time Burden (Hours)	1,470	490
Cost Burden (Dollars)	23,752	19,705

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Abstract: NIMH is requesting OMB approval of this generic plan to continue using various types of information collection instruments in order to achieve our mission and meet our goal of interfacing with the scientific community and promoting the RDoC Initiative.

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Authorizing Statute(s): US Code: 42 USC 285(p) and Section 401(a) Name of Law: 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:
	86 FR 23974	05/05/2021
30-day Notice:	Federal Register Citation:	Citation Date:
	86 FR 36287	07/09/2021
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

table that charts list 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	270	270	0	0	0	0
Annual Time Burden (Hours)	1,470	490	0	980	0	0
Annual Cost Burden (Dollars)	23,752	19,705	0	4,047	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: burden is annualized on SSA, since this is generic we included burden for 3 years

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Annual Cost to Federal Government: $17,687

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.     Yes

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: 07/13/2021

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