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:
0920-1204
ICR Reference No:
202306-0920-014
Status:
Active
Previous ICR Reference No:
202008-0920-004
Agency/Subagency:
HHS/CDC
Agency Tracking No:
0920-1204
Title:
[NCEH] Behavioral Risk Factor Surveillance System (BRFSS) Asthma Call-back Survey (ACBS)
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:
08/11/2023
Retrieve Notice of Action (NOA)
Date Received in OIRA:
07/07/2023
Terms of Clearance:
Previous terms continue: ACBS staff should continue to collaborate with BRFSS staff to transparently present a) joint response rates from BRFSS and ACBS and b) potential non-response bias. Tables of prevalence estimates and risk factors disseminated by CDC (either through its web page or publications) should clearly communicate the caveats of state-to-state comparisons. ACBS should continue to assess options for streamlining the instrument to reduce unnecessary burden and synchronize question wording with recent studies.
Inventory as of this Action
Requested
Previously Approved
Expiration Date
08/31/2026
36 Months From Approved
11/30/2023
Responses
58,772
0
68,846
Time Burden (Hours)
6,073
0
6,615
Cost Burden (Dollars)
0
0
0
Abstract:
The goal is to add depth to the existing body of asthma data and address questions surrounding the health and experiences of persons with asthma. Data are collected through a follow-up survey approximately two weeks after the BRFSS survey. Information is used by asthma control programs in state health departments and at the federal level.
Authorizing Statute(s):
US Code:
42 USC 247
Name of Law: PHSA
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:
88 FR 13825
03/06/2023
30-day Notice:
Federal Register Citation:
Citation Date:
88 FR 43353
07/07/2023
Did the Agency receive public comments on this ICR?
No
Number of Information Collection (IC) in this ICR:
8
IC Title
Form No.
Form Name
ACBS Consent and Survey - Adult
None
ACBS Adult Consent and Questionnaire
ACBS Consent and Survey - Child
None
ACBS Child Consent and Questionnaire
ACBS Data Submission Layout - Adult
ACBS Data Submission Layout - Child
Cell Phone Screener - Adult
None
Cell Phone Screener - Adult
Cellphone Screener - Child
None
Cell Phone Screener - Child
Landline Screener - Adult
None
Landline Screener - Adult
Landline Screener - Child
None
Landline Screener - Child
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
58,772
68,846
0
-10,074
0
0
Annual Time Burden (Hours)
6,073
6,615
0
-542
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:
Yes
Burden Reduction Due to:
Miscellaneous Actions
Short Statement:
Total estimated ACBS burden will decrease due to a reduction in the BRFSS sample which provides the starting point for ACBS sampling and respondents. The proportion of respondents recruited from the landline phone sample will decrease and the proportion of respondents recruited from the cellphone sample will increase. There will be changes to the content of both the adult questionnaire and the child questionnaire. The burden of additional questions will be offset by the deletion of selected questions, therefore the estimated burden per response for each questionnaire will not change., however, the burden per response for the child screener will increase from 1 minute to 2 minutes.
Annual Cost to Federal Government:
$2,200,000
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.
No
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.
No
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:
Renita Macaluso 770 488-6458 arp5@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:
07/07/2023
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