Tourette Syndrome National Education and Outreach Program

Forms and Documents

Document Name	Status
Sup Sta B_Tourette Outreach.docx Supporting Statement B	2011-08-03
Att F_IRB Research Determination.docx Supplementary Document	2011-08-05
Att D comparison of existing and new items.docx Supplementary Document	2011-08-05
Att B_60DayFRN.pdf Supplementary Document	2011-08-03
Att A1_PHSA 2000.pdf Supplementary Document	2011-08-03
Att A2_Children's Health Act 2000.pdf Supplementary Document	2011-08-03
Att E Follow up Survey Invitation.docx Supplementary Document	2011-08-05
Att E Follow up Survey Invitation.docx Supplementary Document	2011-08-05
Sup Sta A_Tourette Outreach.docx Supporting Statement A	2011-08-03

IC Document Collections

IC ID	Document Title	Status
198886	Family Resource Dissemination Other-WORD	New
198885	Family/Public Medical Program Evaluation Other-WORD	New
198884	Family/Public Education Program Evaluation Other-WORD	New
198883	Education Resource Dissemination Other-WORD	New
198882	Education Program Post-test Other-WORD	New
198881	Education Program Pre-Test Other-WORD	New
198880	Education Program Evaluation Other-WORD	New
198879	Medical Resource Dissemination Other-WORD	New
198878	CBIT Program 3-month Follow-up Other-WORD	New
198877	CBIT Online Program Evaluation Other-WORD	New
198876	CBIT Post Test Other-WORD	New
198875	CBIT Pre-test Other-WORD	New
198874	CBIT Program Evaluation Other-WORD	New
198873	Physician Training Retreat 3-Month Follow-up Other-WORD	New
198872	Physician Training Retreat Post-test Other-WORD	New
198871	Physician Training Retreat Pre-test Other-WORD	New
198870	Medical Program Evaluation Instruction	New

ICR Details

OMB Control No: 0920-0901	ICR Reference No: 201108-0920-005
Status: Historical Active	Previous ICR Reference No:
Agency/Subagency: HHS/CDC	Agency Tracking No:
Title: Tourette Syndrome National Education and Outreach Program
Type of Information Collection: New collection (Request for a new OMB Control Number)	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 09/27/2011
	Date Received in OIRA: 08/15/2011
Terms of Clearance:

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	09/30/2013	24 Months From Approved
Responses	7,100	0	0
Time Burden (Hours)	277	0	0
Cost Burden (Dollars)	0	0	0

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Abstract: The National Center for Birth Defects and Developmental Disabilities will collect program evaluation data from participants of educational workshops and recipients of educational resources on Tourette Syndrome (TS) conducted by the Tourette Syndrome Association in a cooperative agreement with the CDC. Health education has been developed for three groups of audiences: Health professionals, education professionals, and people with TS and their families. The format includes general education programs for the three groups, as well as two more in-depth medical training programs for physicians on TS and on the Comprehensive Behavioral Intervention for Tics (CBIT) treatment.

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Authorizing Statute(s): US Code: 42 USC 241 Name of Law: The Public Health and Welfare
  

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:
	76 FR 7860	02/11/2011
30-day Notice:	Federal Register Citation:	Citation Date:
	76 FR 45257	07/28/2011
Did the Agency receive public comments on this ICR? Yes

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Number of Information Collection (IC) in this ICR: 17

IC Title	Form No.	Form Name
Medical Program Evaluation
Physician Training Retreat Pre-test
Physician Training Retreat Post-test
Physician Training Retreat 3-Month Follow-up
CBIT Program Evaluation
CBIT Pre-test
Education Resource Dissemination
CBIT Post Test
CBIT Online Program Evaluation
Medical Resource Dissemination
Education Program Evaluation
Education Program Pre-Test
Education Program Post-test
Family/Public Education Program Evaluation
Family/Public Medical Program Evaluation
Family Resource Dissemination
CBIT Program 3-month Follow-up

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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	7,100	0	0	7,100	0	0
Annual Time Burden (Hours)	277	0	0	277	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 a new information collection.

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Annual Cost to Federal Government: $1,131,326

Does this IC contain surveys, censuses, or employ statistical methods? Yes Part B of Supporting Statement

Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002? 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? 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: 08/15/2011

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