WASHINGTON, DC, METROPOLITAN AREA DRUG STUDY (DC*MADS)

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
112018	WASHINGTON, DC, METROPOLITAN AREA DRUG STUDY (DC*MADS)	Migrated

ICR Details

OMB Control No: 0930-0145	ICR Reference No: 199107-0930-001
Status: Historical Active	Previous ICR Reference No: 199010-0930-001
Agency/Subagency: HHS/SAMHSA	Agency Tracking No:
Title: WASHINGTON, DC, METROPOLITAN AREA DRUG STUDY (DC*MADS)
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 10/24/1991
	Date Received in OIRA: 07/15/1991
Terms of Clearance: Approved for use under the conditions that the next submission for OMB review must include: 1) A thorough justification for remuneration policies (with evidence of reduced non response rates) and a reconsideration of such policies. NIDA may need to establish a control group for this analysi 2) A thorough discussion of the data limitations in each module of DC MADS and whether DC MADS findings are representative of the Distric of Columbia, as well as other metropolitan areas; and 3) A reevaluation of the practical utility of this data in light of the limitations addressed above and rising unit costs of this effort.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	08/31/1992	08/31/1992	12/31/1991
Responses	9,845	0	8,556
Time Burden (Hours)	9,845	0	8,556
Cost Burden (Dollars)	0	0	0

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Abstract: DC*MADS WILL COLLECT DATA ABOUT THE PREVALENCE, INCIDENCE, AND CONSEQUENCES OF DRUG ABUSE AMONG NONHOUSEHOLD AND HARD-TO-REACH POPULATIONS IN ONE METROPLOLITAN AREA AND WILL INTEGRATE THE FINDINGS WITH NHSDA DATA ABOUT THE HOUSEHOLD POPULATION IN THE SAME AREA. SURV AND RECORD DATA WILL BE COLLECTED FROM POPULATION SUBGROUPS SUCH AS

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Authorizing Statute(s): None

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:

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Federal Register Notices & Comments

Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 1

IC Title	Form No.	Form Name
WASHINGTON, DC, METROPOLITAN AREA DRUG STUDY (DC*MADS)

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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	9,845	8,556	0	1,289	0	0
Annual Time Burden (Hours)	9,845	8,556	0	1,289	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:

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: $0

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

Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002? No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? Uncollected

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? Uncollected

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? Uncollected

Is this ICR related to the Pandemic Response? Uncollected

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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: 07/15/1991

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