Balance After Baby Intervention

ICR 201711-0920-001

OMB: 0920-1115

Federal Form Document

Forms and Documents
Document
Name
Status
Form and Instruction
Unchanged
Form and Instruction
Modified
Form and Instruction
Modified
Form and Instruction
Modified
Form and Instruction
Modified
Form and Instruction
Modified
Form and Instruction
Unchanged
Justification for No Material/Nonsubstantive Change
2017-11-02
Supplementary Document
2016-01-21
Supplementary Document
2016-01-21
Supplementary Document
2016-01-21
Supplementary Document
2016-01-21
Supporting Statement B
2016-01-21
Supporting Statement A
2016-01-21
ICR Details
0920-1115 201711-0920-001
Historical Active 201601-0920-012
HHS/CDC 0920-18DR
Balance After Baby Intervention
No material or nonsubstantive change to a currently approved collection   No
Regular
Approved without change 11/09/2017
Retrieve Notice of Action (NOA) 11/03/2017
  Inventory as of this Action Requested Previously Approved
06/30/2019 06/30/2019 06/30/2019
698 0 698
187 0 183
0 0 0

Information will be collected from postpartum women with recent gestational diabetes mellitus (GDM). A randomized controlled clinical trial will be conducted to evaluate the effectiveness of a web-based lifestyle intervention program that may promote weight management and reduce risk of developing type 2 diabetes.

US Code: 24 USC 42 Name of Law: Public Health Service Act, Research and Investigations
  
None

Not associated with rulemaking

  80 FR 52292 08/28/2015
81 FR 3426 01/21/2016
No

  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 698 698 0 0 0 0
Annual Time Burden (Hours) 187 183 0 4 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
Yes
Miscellaneous Actions
No
Minor changes are planned to (I) improve tracking of participation in other programs, (ii) clarify the wording of one question, (iii) clarity how burden is communicated to participants, and (iv) collect systematic feedback from participants. Changes increase total estimated annualized burden by 4 hours.

$500,000
Yes Part B of Supporting Statement
    No
    No
No
No
No
Uncollected
Renita Macaluso 770 488-6458 arp5@cdc.gov

  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:
 
 
 
 
 
 
 
    (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;
 
 
 
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.
11/03/2017


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