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View Information Collection (IC) List
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Please note that the OMB number and expiration date may not have been determined when this Information Collection Request and associated Information Collection forms were submitted to OMB. The approved OMB number and expiration date may be found by clicking on the Notice of Action link below.
View Generic ICR - OIRA Conclusion
OMB Control No:
0920-0800
ICR Reference No:
201408-0920-009
Status:
Historical Active
Previous ICR Reference No:
201111-0920-004
Agency/Subagency:
HHS/CDC
Agency Tracking No:
Title:
Focus Group Testing to Effectively Plan and Tailor Cancer Prevention and Control Communication Campaigns
Type of Information Collection:
Extension without change of a currently approved collection
Common Form ICR:
No
Type of Review Request:
Regular
OIRA Conclusion Action:
Approved without change
Conclusion Date:
12/08/2014
Retrieve Notice of Action (NOA)
Date Received in OIRA:
09/12/2014
Terms of Clearance:
Previous terms of clearance continue: This generic clearance for HHS/CDC Focus Group Testing to Effectively Plan and Tailor Cancer Prevention and Control Communication Campaigns is approved under the following conditions: 1) HHS/CDC shall use the generic clearance to collect general public and health care professionals data (via focus groups) where the agency seeks to gather information for general service improvement, not for publication or for the purpose of informing significant policy or resource allocation decisions. 2) Focus groups should be of limited size and scope. 3) For individual focus groups, HHS/CDC shall submit a generic IC in ROCIS along with an abbreviated supporting statement in the template agreed to by OMB and HHS/CDC. This statement shall include all relevant information, including a statement of need, intended use of information, description of respondents, information collection procedures, expected response rate, justification for incentive, and estimated burden. 4) OMB will aim to respond with clearance or questions within 10 working days.
Inventory as of this Action
Requested
Previously Approved
Expiration Date
12/31/2017
36 Months From Approved
12/31/2014
Responses
7,200
0
2,592
Time Burden (Hours)
5,040
0
1,814
Cost Burden (Dollars)
81,934
0
52,843
Abstract:
CDC conducts focus groups and interviews to collect the information needed to plan and tailor communication campaigns for colorectal cancer, gynecologic cancer, and other cancers. These efforts are supported by a generic clearance dedicated to formative research with the general public, health care professionals, and other targeted audiences.
Authorizing Statute(s):
US Code:
42 USC 301
Name of Law: Public Health Service Act
US Code:
42 USC 247b-17
Name of Law: Gynecologic Cancer Education and Awareness Act, Johanna's Law
Citations for New Statutory Requirements:
None
Associated Rulemaking Information
RIN:
Stage of Rulemaking:
Federal Register Citation:
Date:
Not associated with rulemaking
Federal Register Notices & Comments
60-day Notice:
Federal Register Citation:
Citation Date:
79 FR 36065
06/25/2014
30-day Notice:
Federal Register Citation:
Citation Date:
79 FR 52011
09/02/2014
Did the Agency receive public comments on this ICR?
No
Number of Information Collection (IC) in this ICR:
6
IC Title
Form No.
Form Name
2015 Focus Group Testing with General Public
none, none, none, none
Screener and Recruitment
,
Screener and Recruitment - Spanish
,
Focus Group Guide
,
Focus Group Guide - Spanish
Assessing Satisfaction with Technical Assistance (TA) Provided to Racial and Ethnic Approaches to Community Health (REACH) Awardees
Focus Group Testing to Effectively Plan and Tailor "Bring Your Brave" Communication Campaign Messages
Focus Group Testing to Effectively Plan and Tailor a Communication Campaign about Young Women and Breast Cancer
0920-0800, 0920-0800, 0920-0800, 0920-0800, 0920-0800, 0920-0800, 0920-0800, 0920-0800, 0920-0800, 0920-0800, 0920-0800
B2 - Materials for Testing_AJ (Family History)_4 09 2015
,
C1 - Discussion Guide for AJ (No Family History)_04 09 2015
,
C2 - Materials for Testing_AJ (No Family History)_4 09 2015
,
D1 - Discussion Guide for AA (Family History)_04 09 2015
,
D2 - Materials for Testing_AA (Family History)_4 09 2015
,
E1 - Discussion Guide for AA (No Family History)_04 09 2015
,
F1 - Discussion Guide Other (Family History)_04 09 2015
,
F2 - Materials for Testing_Other (Family History)_4 09 2015
,
H - Screening Instrument for Ashkenazi Jewish Young Women
,
I - Screening Instrument for African American Young Women
,
J - Screening Instrument for Other Young Women
Focus Groups Assessing the Uptake and Effectiveness of Inside Knowledge: Get the Facts About Gynecologic Cancer Campaign Materials
NA, NA, NA
Recruitment Form - Hispanic
,
Recruitment Form -Low SES
,
Recruitment Form - Disabilities
Formative Research Legionella
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
7,200
2,592
0
4,608
0
0
Annual Time Burden (Hours)
5,040
1,814
0
3,226
0
0
Annual Cost Burden (Dollars)
81,934
52,843
0
29,091
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 an Extension ICR with a small reduction in Burden; the numbers previously presented were not for three years of clearance.
Annual Cost to Federal Government:
$482,000
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
Agency Contact:
Shari Steinberg 404 639-4942 sxw2@cdc.gov
Common Form ICR:
No
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:
09/12/2014