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:
0920-0743
ICR Reference No:
201308-0920-008
Status:
Historical Active
Previous ICR Reference No:
201106-0920-005
Agency/Subagency:
HHS/CDC
Agency Tracking No:
20306
Title:
Assessment & Monitoring of Breastfeeding-Related Maternity Care Practices in Intrapartum Care Facilities in the United States and Territories
Type of Information Collection:
Reinstatement with change of a previously approved collection
Common Form ICR:
No
Type of Review Request:
Regular
OIRA Conclusion Action:
Approved without change
Conclusion Date:
09/23/2013
Retrieve Notice of Action (NOA)
Date Received in OIRA:
08/16/2013
Terms of Clearance:
Inventory as of this Action
Requested
Previously Approved
Expiration Date
09/30/2016
36 Months From Approved
Responses
6,595
0
0
Time Burden (Hours)
1,103
0
0
Cost Burden (Dollars)
0
0
0
Abstract:
CDC plans to conduct a census survey of all intra-partum care facilities in the U.S. and territories about the facilities' maternity care practices focused on care and support for breastfeeding throughout the maternity stay. This ICR requests administration of two iterations of the survey (in 2013 and 2015) spanning the requested three-year ICR approval period using methodology similar to that established and carried out in previous surveys conducted in 2007, 2009, and 2011.
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:
78 FR 9924
02/12/2013
30-day Notice:
Federal Register Citation:
Citation Date:
78 FR 49523
08/14/2013
Did the Agency receive public comments on this ICR?
Yes
Number of Information Collection (IC) in this ICR:
3
IC Title
Form No.
Form Name
2011 mPINC Survey for Birth Centers
none
Birth Center Survey
Screening Telephone Call Script -- Part B (eligibles only)
Screening Telephone Call Script_Part A (all respondents)
mPINC (National Survey of Maternity Practices in Infant Nutrition and Care) Survey (for ALL facilities)
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
6,595
0
0
6,595
0
0
Annual Time Burden (Hours)
1,103
0
0
1,103
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:
Changes described in this ICR include: (1) a reduction in the number of respondents and a net reduction of 583 burden hours. Reductions are primarily due to the effects of annualization; (2) Reduction in the estimated burden for screening. In previous approval periods, we assigned the same burden to both eligible and ineligible respondents. In this Reinstatement, we only assign the complete burden for screening to eligible facilities that complete all screening questions. The previous OMB approval covered one cycle of data collection in 2011. In the current Reinstatement ICR, we request OMB approval for a period of three years to support two cycles of data collection in 2013 and 2015. Although the estimated number of participating facilities is almost identical for each cycle of data collection (2,690 facilities in 2011; 2,738 facilities in 2013; and 2,738 facilities in 2015), the process of annualization results in "apparent" reductions in both the annualized number of respondents and the total estimated annualized burden. However, there is only a minor adjustment to the estimated number of facilities participating in 2013 and 2015, and there is no change to the estimated burden per response (30 minutes). Similarly, in 2011 we estimated that 3,989 facilities would participate in the screening process. For 2013 and 2015, we estimate that 2,570 facilities will participate in screening on an annualized basis. In addition to a slight absolute decrease in screened respondents, annualization results in an apparent decrease in the annualized number of respondents. In this Reinstatement ICR, we also distinguish between screening burden for eligible facilities (average total burden per response of 5 minutes), and screening burden for ineligible facilities (average burden per response of one minute). The previous ICR used a simple 5 minute estimate for all respondents who participated in the screening process. The result is a net decrease in total estimated annualized response burden for screening, although there are no substantive changes to the screening process. There are no substantive changes to survey content.
Annual Cost to Federal Government:
$426,167
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:
Thelma Sims 4046394771
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:
08/16/2013
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