View Information Collection Request (ICR) Package
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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 ICR - OIRA Conclusion
OMB Control No:
0920-1333
ICR Reference No:
202106-0920-010
Status:
Historical Active
Previous ICR Reference No:
202010-0920-014
Agency/Subagency:
HHS/CDC
Agency Tracking No:
0920-20FO
Title:
Feeding My Baby and Me: Infant Feeding Practices Study III
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:
06/29/2021
Retrieve Notice of Action (NOA)
Date Received in OIRA:
06/24/2021
Terms of Clearance:
Previous terms continue: The data collected from this collection is not generalizable beyond the respondents and in all publications and discussions, CDC will characterize these limitations on generalizability due to the sampling approach.
Inventory as of this Action
Requested
Previously Approved
Expiration Date
04/30/2024
04/30/2024
04/30/2024
Responses
23,352
0
23,352
Time Burden (Hours)
5,052
0
5,052
Cost Burden (Dollars)
143,685
0
143,685
Abstract:
The Feeding My Baby and Me: Infant Feeding Practices Study III (IFPS III) is a longitudinal study that will follow pregnant women and their new baby for two years. This study will assess the current state of mothers' intentions, behaviors, feeding decisions, and practices from pregnancy through their child's first two years of life, assess how these change, and their association with different health outcomes. Data will be used to inform CDC's programmatic work to improve feeding practices.
Authorizing Statute(s):
US Code:
42 USC 241
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:
85 FR 29453
05/15/2020
30-day Notice:
Federal Register Citation:
Citation Date:
85 FR 80109
12/11/2020
Did the Agency receive public comments on this ICR?
Yes
Number of Information Collection (IC) in this ICR:
22
IC Title
Form No.
Form Name
1-Month Survey
0920-20FO
Att.4d-Month 1 Survey-Revised
10-Month Survey
0920-20FO
Att.4k-Month 10 Survey-Revised
12-Month Survey
0920-20FO
Att.4l-Month12 Survey-Revised
15-Month Survey
092-20FO
Att.4m-Month 15 Survey-Revised
18-Month Survey
0920-20FO
Att.4n-Month 18 Survey-Revised
2-Month Survey
0920-20FO
Attachment 4e – Month 2 survey- Revised
21-Month Survey
0920-20FO
Att.4o-Month 21 Survey-Revised
24-Month Survey
092-20FO
Attachment 4p – Month 24 survey-Revised
3-Month 24-Hour Dietary Recall
n/a
ASA24
3-Month 24-Hour Dietary Recall (Replicate)
n/a
ASA24
3-Month Survey
0920-20FO
Att.4f-Month 3 Survey-Revised
4-Month Survey
0920-20FO
Att.4g-Month 4 Survey-Revised
5-Month Survey
0920-20FO
Att.4h-Month 5 Survey-Revised
6-Month Survey
0920-20FO
Att.4i-Month 6 Survey-Revised
8-Month Survey
0920-20FO
Att.4j-Month 8 Survey-Revised
Birth Screener
n/a
Birth Screener
Prenatal 24-Hour Dietary Recall
n/a
ASA24
Prenatal 24-Hour Dietary Recall (Replicate)
n/a
ASA24
Prenatal Survey
0920-20FO
Att.4b-Prenatal Survey-Revised
Request for Notification of Child's Birth
n/a
Request for Notification of Child's Birth
Screening
n/a
Screener
Study Consent and Contact Information
n/a
Informed Consent and Contact Information
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
23,352
23,352
0
0
0
0
Annual Time Burden (Hours)
5,052
5,052
0
0
0
0
Annual Cost Burden (Dollars)
143,685
143,685
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:
Annual Cost to Federal Government:
$683,294
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?
No
Agency Contact:
Odion Clunis 770 488-0045 lta2@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:
06/24/2021
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