View Information Collection Request (ICR) Package
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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:
0925-0046
ICR Reference No:
201907-0925-007
Status:
Historical Active
Previous ICR Reference No:
201605-0925-007
Agency/Subagency:
HHS/NIH
Agency Tracking No:
19122
Title:
Formative Research, Pretesting, and Customer Satisfaction of NCI's Communication and Education Resources (NCI)
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:
11/05/2019
Retrieve Notice of Action (NOA)
Date Received in OIRA:
07/30/2019
Terms of Clearance:
NIH will submit individual collections under this generic clearance to OMB. OMB will strive to provide feedback on the individual collections within ten working days, whenever possible. These submissions will include the actual study instruments, and each IC request should continue include a justification for the chosen incentive, if beyond the standard incentive amount of $40 (e.g. difficult recruitments, two hour focus groups etc.)
Inventory as of this Action
Requested
Previously Approved
Expiration Date
11/30/2022
36 Months From Approved
11/30/2019
Responses
54,000
0
108,000
Time Burden (Hours)
40,500
0
7,200
Cost Burden (Dollars)
0
0
0
Abstract:
This is a request for OMB to approve a revision for this generic submission for three years. As part of NCI’s mandate from Congress to disseminate information on cancer research, detection, prevention, and treatment, the Institute develops a wide variety of messages and materials. Testing these messages and materials assesses their potential effectiveness in reaching and communicating with their intended audience while they are still in the developmental stage and can be revised.
Authorizing Statute(s):
US Code:
42 USC 285a-2
Name of Law: Public Health Service Act
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:
84 FR 13670
04/05/2019
30-day Notice:
Federal Register Citation:
Citation Date:
84 FR 36612
07/30/2019
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
Alcohol Information Audience Needs Assessment (NIAAA)
2, 1, 3, 4
Online survey Screener and consent form
,
Online survey
,
Focus Group Screener
,
Focus Group Consent Form
Evaluation of Office of Acquisitions System (OASYS) and FFRDC Contract Administration System (FCAS) Vendor Portals (NCI)
6, 1, 2, 3, 4, 5
OASYS Vendor Portal Registration
,
FCAS Vendor Portal Registration
,
Survey OASYS
,
FCAS Survey
,
OASYS Data Field Vendor Portal Screenshots
,
FCAS Data Field Vendor Portal Screenshots
NCI Community Oncology Research Program (NCORP) Practice Survey of Site Level Attributes (NCI)
1
NCORP Program Site Level Attributes Survey
Office of Research Training and Development (ORTD) Application Form for electronic Individual Development Plan (eIDP) (NIAID)
1
initial Trainee eIDP screenshot
Personas and Journey Mapping: Business Audience (NCI)
4, 5, 1, 3, 2
SBIR Awardees and Prospects Business Audience
,
Investing Business Audience
,
Co-Developing and Licensing Business Audience
,
Intramural Researchers Audience
,
Questionnaire
Write the Vision Program Formative Research (NEI)
2, 1
NEI WTV screener
,
NEI WTV Moderators Guide
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
54,000
108,000
0
-54,000
0
0
Annual Time Burden (Hours)
40,500
7,200
0
33,300
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 information collection request is a revision, due to an increase in the incentives to the respondents, the proposed incentive amount for Physicians has been increased by $50.00, and for Individuals (General Public) by $25.00, a reduction in the number of respondents from 18,000 per year to 9,000 per year, and the Average Time Per Response (in hours) from 12 minutes to 45 minutes, which will increase our Burden Hours from 7,200 to 13,500. As discussed in A.9, the proposed incentive amount increases for Physicians and for Individuals (General Public) will ensure that NCI can attract hard-to-recruit populations to improve response rates, data quality, and motivate respondents to participate.
Annual Cost to Federal Government:
$300,095
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.
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?
Uncollected
Agency Contact:
Tawanda Abdelmouti 240 276-5530 ta401@nih.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:
07/30/2019