[NCIPC] Comprehensive Evaluation of the Implementation and Uptake of the CDC Clinical Practice Guideline for Prescribing Opioids for Pain

Forms and Documents

Document Name	Status

No forms / supporting documents in this ICR. Check IC Document Collections.

IC Document Collections

IC ID	Document Title	Status
272991	Caregiver Focus Groups Form and Instruction	Unchanged
272989	Patient Focus Groups Form and Instruction	Unchanged
272988	Medical Board Leaders Interview Form and Instruction	Unchanged
272987	Professional Association Leaders Interview Form and Instruction	Unchanged
272986	Payer Interview Form and Instruction	Unchanged
272985	Health System Leaders Interview Form and Instruction	Unchanged
272984	Dentist Interview Form and Instruction	Unchanged
272983	Clinician Interview Form and Instruction	Unchanged
272982	Clinician - Follow-Up Emails Form and Instruction	Unchanged
272981	Clinician - Invitation Form and Instruction	Unchanged
272978	Clinician - Clinician Survey Form and Instruction	Modified

ICR Details

OMB Control No: 0920-1459	ICR Reference No: 202603-0920-005
Status: Active	Previous ICR Reference No: 202508-0920-009
Agency/Subagency: HHS/CDC	Agency Tracking No: 0920-26-0130
Title: [NCIPC] Comprehensive Evaluation of the Implementation and Uptake of the CDC Clinical Practice Guideline for Prescribing Opioids for Pain
Type of Information Collection: No material or nonsubstantive change to a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 03/09/2026
Retrieve Notice of Action (NOA)	Date Received in OIRA: 03/09/2026
Terms of Clearance:

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	06/30/2028	06/30/2028	06/30/2028
Responses	2,311	0	2,311
Time Burden (Hours)	310	0	310
Cost Burden (Dollars)	0	0	0

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Abstract: Data collection is designed to conduct a comprehensive evaluation of the dissemination, implementation, and outcomes of the CDC Clinical Practice Guideline for Prescribing Opioids for Pain – United States, 2022 (2022 CDC Clinical Practice Guideline). Resulting data will be used for purposes of evaluation and to ensure that Americans have access to safer, effective ways of managing their pain. This change request is submitted to comply with recent executive orders.The requested changes are necessary due to change in contracting partners.

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Authorizing Statute(s): US Code: 42 USC 241 Name of Law: U.S. PHSA
  

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:
	89 FR 79925	10/01/2024
30-day Notice:	Federal Register Citation:	Citation Date:
	89 FR 104159	12/20/2024
Did the Agency receive public comments on this ICR? Yes

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Number of Information Collection (IC) in this ICR: 11

IC Title	Form No.	Form Name
Caregiver Focus Groups	N/A	Caregiver Focus Group Guide
Clinician - Clinician Survey	N/A, 0920-26-0130	Clinician Survey ,   Clinican Survey
Clinician - Follow-Up Emails	N/A	Clinician Follow-Up Email
Clinician - Invitation	N/A	Clinician Invitation
Clinician Interview	N/A	Clinician Interview Guide
Dentist Interview	N/A	Dentist Interview Guide
Health System Leaders Interview	N/A	Health System Leaders Interview Guide
Medical Board Leaders Interview	N/A	Medical Board Leaders Interview Guide
Patient Focus Groups	N/A	Patient Focus Group Guide
Payer Interview	N/A	Payer Interview Guide
Professional Association Leaders Interview	N/A	Professional Association Leaders Interview Guide

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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	2,311	2,311	0	0	0	0
Annual Time Burden (Hours)	310	310	0	0	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

Burden increases because of Program Change due to Agency Discretion: No

Burden Increase Due to:

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement:

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Annual Cost to Federal Government: $1,024,101

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)? Yes

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: 03/09/2026

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