Agency Forms Undergoing Paperwork Reduction Act Review, 44568-44569 [2013-17799]

Download as PDF 44568 Federal Register / Vol. 78, No. 142 / Wednesday, July 24, 2013 / Notices This information will allow CDC to compile a systematic, quantifiable inventory of preference data for a group that is considered representative of tractor parts dealers nationwide. It will also allow CDC to develop 39 hours which is based on a reduced response rate of 90% (468 respondents), as indicated in the table below. The average burden per response is 5 minutes. There are no costs to respondents other than their time. recommendations for overcoming the barriers that have compromised the effectiveness of occupational health and safety programs. The total estimated burden for the one-time retrospective data collection is ESTIMATED ANNUALIZED BURDEN HOURS Type of respondents Tractor Parts Dealers ........................ Total ........................................... ROPS Questionnaire Parts Dealers. 1 5/60 39 ........................................................... ........................ ........................ ........................ 39 BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day–13–13PV] Agency Forms Undergoing Paperwork Reduction Act Review The Centers for Disease Control and Prevention (CDC) publishes a list of information collection requests under review by the Office of Management and Budget (OMB) in compliance with the Paperwork Reduction Act (44 U.S.C. Chapter 35). To request a copy of these requests, call (404) 639–7570 or send an email to omb@cdc.gov. Send written comments to CDC Desk Officer, Office of Management and Budget, Washington, DC 20503 or by fax to (202) 395–5806. Written comments should be received within 30 days of this notice. Proposed Project sroberts on DSK5SPTVN1PROD with NOTICES Study to Explore Educational Children’s Book in Pediatric Offices— NEW—National Center on Birth Defects and Developmental Disabilities (NCBDDD), Centers for Disease Control and Prevention (CDC). Background and Brief Description Using a children’s picture book format, CDC developed Amazing Me: It’s Busy Being 3! to increase awareness of 16:35 Jul 23, 2013 Total burden (in hrs) 468 [FR Doc. 2013–17740 Filed 7–23–13; 8:45 am] Jkt 229001 for Average burden per response (in hrs) Tractor Leroy A. Richardson, Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. VerDate Mar<15>2010 Number of responses per respondent Number of respondents Form name developmental milestones among parents of 3-year-old children and actively engage them in the monitoring of their child’s development. CDC partnered with Lysol and Reach Out and Read (ROR), a non-profit organization that promotes early literacy among lowincome families by distributing books in pediatric exam rooms, to disseminate copies of Amazing Me to parents. In Spring 2012, 250 of RoR’s largest pediatric clinics each received 300 copies of Amazing Me for distribution to parents of 3-year-old children during well-child visits. Distribution of Amazing Me through RoR practices was used as a vehicle to reach those at higher risk for developmental delays and disabilities: Children insured by Medicaid and children from families with low incomes. Preliminary data gathered from a web survey of RoR clinic staff indicates that clinic staff are not only receptive to but supportive of the Amazing Me book. However, the web survey of RoR clinic staff does not provide information from the book’s target audience: Parents. If CDC wishes to expand book distribution beyond ROR clinic settings, it will be important to gather data on parents’ experiences receiving the Amazing Me book as part of a pediatric visit, and what kind of influence, if any, the book has had on their knowledge, attitudes, and beliefs about developmental milestones. To this end, CDC will identify and recruit three ROR pediatric practices and three non-ROR practices in the greater Atlanta, Georgia and greater Washington, DC areas to distribute copies of Amazing Me to parents/ guardians of 3 year olds, soon to be 3 year olds, or recently turned 4 year olds attending the selected practices. The PO 00000 Frm 00050 Fmt 4703 Sfmt 4703 study will gather feedback from parents/ guardians about (1) their experiences receiving the book as part of a pediatric visit, and (2) the influence of the book on their awareness, attitudes, and selfefficacy regarding monitoring developmental milestones. Findings from the parent web survey and focus groups will help CDC to determine if a children’s book is an effective channel for reaching parents, whether more books like Amazing Me for other age groups should be developed, and if the ROR book distribution model is an effective means to reach low-income and at-risk families. Data will be gathered through a web survey of 900 parents/guardians who have received a copy of the Amazing Me book from participating ROR and nonROR practices. Parents/guardians will access the web survey by logging onto a URL address provided on a sticker affixed to the inside cover of each Amazing Me book. All survey responses (100%) will be submitted through a secure survey Web site established for this project. CDC will also conduct six follow-up focus groups with survey respondents to gather more in-depth information from parents about their experiences reading the Amazing Me book at home with their children and assessing their child’s development using the book. We estimate that we will screen 60 parents/ guardians to recruit 54 participants for the focus groups. These six focus groups will be conducted in greater Atlanta, Georgia (2) and greater Washington, DC (4). This request is submitted to obtain OMB clearance for one year. The estimated annualized burden is 229 hours. There are no costs to the respondents other than their time. E:\FR\FM\24JYN1.SGM 24JYN1 44569 Federal Register / Vol. 78, No. 142 / Wednesday, July 24, 2013 / Notices ESTIMATED ANNUALIZED BURDEN HOURS Type of respondent Parents/Guardians Parents/Guardians Parents/Guardians Parents/Guardians Parents/Guardians .......................................... .......................................... .......................................... .......................................... .......................................... __________________________________ Leroy A. Richardson, Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2013–17799 Filed 7–23–13; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services [Document Identifier: CMS–10268, CMS– 10287, CMS–R–70, CMS–R–72, CMS–R–247, CMS–10151, CMS–10380, CMS–10286, and CMS–10339] Agency Information Collection Activities: Submission for OMB Review; Comment Request ACTION: Notice. The Centers for Medicare & Medicaid Services (CMS) is announcing an opportunity for the public to comment on CMS’ intention to collect information from the public. Under the Paperwork Reduction Act of 1995 (PRA), Federal agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension or reinstatement of an existing collection of information, and to allow a second opportunity for public comment on the notice. Interested persons are invited to send comments regarding the burden estimate or any other aspect of this collection of information, including any of the following subjects: (1) The necessity and utility of the proposed information collection for the proper performance of the agency’s functions; (2) the accuracy of the estimated burden; (3) ways to enhance the quality, utility, and clarity of the information to be collected; and (4) the use of automated collection techniques or other forms of information technology to minimize the information collection burden. sroberts on DSK5SPTVN1PROD with NOTICES SUMMARY: VerDate Mar<15>2010 16:35 Jul 23, 2013 Jkt 229001 Number of respondents Form name Web Survey .................................................... Follow-up web survey .................................... Focus Group Screener ................................... Focus Group Informed Consent .................... Focus Group Moderator ................................. Comments on the collection(s) of information must be received by the OMB desk officer by August 23, 2013. ADDRESSES: When commenting on the proposed information collections, please reference the document identifier or OMB control number. To be assured consideration, comments and recommendations must be received by the OMB desk officer via one of the following transmissions: OMB, Office of Information and Regulatory Affairs, Attention: CMS Desk Officer, Fax Number: (202) 395–6974, or Email: OIRA_submission@omb.eop.gov. To obtain copies of a supporting statement and any related forms for the proposed collection(s) summarized in this notice, you may make your request using one of following: 1. Access CMS’ Web site address at https://www.cms.hhs.gov/ PaperworkReductionActof1995. 2. Email your request, including your address, phone number, OMB number, and CMS document identifier, to Paperwork@cms.hhs.gov. 3. Call the Reports Clearance Office at (410) 786–1326. FOR FURTHER INFORMATION CONTACT: Reports Clearance Office at (410) 786– 1326. SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501–3520), Federal agencies must obtain approval from the Office of Management and Budget (OMB) for each collection of information they conduct or sponsor. The term ‘‘collection of information’’ is defined in 44 U.S.C. 3502(3) and 5 CFR 1320.3(c) and includes agency requests or requirements that members of the public submit reports, keep records, or provide information to a third party. Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A)) requires Federal agencies to publish a 30-day notice in the Federal Register concerning each proposed collection of information, including each proposed extension or reinstatement of an existing collection of information, before submitting the collection to OMB for approval. To comply with this requirement, CMS is DATES: PO 00000 Frm 00051 Fmt 4703 Sfmt 4703 900 900 60 54 54 Number of responses per respondent 1 1 1 1 1 Average burden per response (in hours) 10/60 1/60 5/60 5/60 1 publishing this notice that summarizes the following proposed collection(s) of information for public comment: 1. Type of Information Collection Request: Reinstatement of a currently approved collection; Title of Information Collection: Consolidated Renal Operations in a Web Enabled Network (CROWNWeb) Third-party Submission Authorization Form; Use: The Consolidated Renal Operations in a Web Enabled Network (CROWNWeb) Third-Party Submission Authorization form (CWTPSA) is to be completed by ‘‘Facility Administrators’’ (administrators of CMS-certified dialysis facilities) if they intend to authorize a third party (a business with which the facility is associated, or an independent vendor) to submit data to us to comply with the recently-revised Conditions for Coverage of dialysis facilities. The CROWNWeb system is the system used as the collection point of data necessary for entitlement of ESRD patients to Medicare benefits and for Federal Government monitoring and assessing of the quality and types of care provided to renal patients. The information collected through the CWTPSA form will allow us along with our contractors to receive data from authorized parties acting on behalf of CMS-certified dialysis facilities. Since February 2009, we have received 4,160 CWTPSA forms and anticipates that they will continue to receive no more than 400 new CWTPSA forms annually to address the creation of new facilities under the current participating ‘‘third party submitters.’’ Form Number: CMS–10268 (OCN: 0938–1052); Frequency: Occasionally; Affected Public: Private Sector—Business or other for-profits and Not-for-profit institutions; Number of Respondents: 400; Total Annual Responses: 400; Total Annual Hours: 34. (For policy questions regarding this collection contact Michelle Tucker at 410–786–0736.) 2. Type of Information Collection Request: Extension of a currently approved collection; Title of Information Collection: Medicare Quality of Care Complaint Form; Use: In E:\FR\FM\24JYN1.SGM 24JYN1

Agencies

[Federal Register Volume 78, Number 142 (Wednesday, July 24, 2013)]
[Notices]
[Pages 44568-44569]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-17799]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30Day-13-13PV]


Agency Forms Undergoing Paperwork Reduction Act Review

    The Centers for Disease Control and Prevention (CDC) publishes a 
list of information collection requests under review by the Office of 
Management and Budget (OMB) in compliance with the Paperwork Reduction 
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call 
(404) 639-7570 or send an email to omb@cdc.gov. Send written comments 
to CDC Desk Officer, Office of Management and Budget, Washington, DC 
20503 or by fax to (202) 395-5806. Written comments should be received 
within 30 days of this notice.

Proposed Project

    Study to Explore Educational Children's Book in Pediatric Offices--
NEW--National Center on Birth Defects and Developmental Disabilities 
(NCBDDD), Centers for Disease Control and Prevention (CDC).

Background and Brief Description

    Using a children's picture book format, CDC developed Amazing Me: 
It's Busy Being 3! to increase awareness of developmental milestones 
among parents of 3-year-old children and actively engage them in the 
monitoring of their child's development. CDC partnered with Lysol and 
Reach Out and Read (ROR), a non-profit organization that promotes early 
literacy among low-income families by distributing books in pediatric 
exam rooms, to disseminate copies of Amazing Me to parents. In Spring 
2012, 250 of RoR's largest pediatric clinics each received 300 copies 
of Amazing Me for distribution to parents of 3-year-old children during 
well-child visits. Distribution of Amazing Me through RoR practices was 
used as a vehicle to reach those at higher risk for developmental 
delays and disabilities: Children insured by Medicaid and children from 
families with low incomes.
    Preliminary data gathered from a web survey of RoR clinic staff 
indicates that clinic staff are not only receptive to but supportive of 
the Amazing Me book. However, the web survey of RoR clinic staff does 
not provide information from the book's target audience: Parents. If 
CDC wishes to expand book distribution beyond ROR clinic settings, it 
will be important to gather data on parents' experiences receiving the 
Amazing Me book as part of a pediatric visit, and what kind of 
influence, if any, the book has had on their knowledge, attitudes, and 
beliefs about developmental milestones.
    To this end, CDC will identify and recruit three ROR pediatric 
practices and three non-ROR practices in the greater Atlanta, Georgia 
and greater Washington, DC areas to distribute copies of Amazing Me to 
parents/guardians of 3 year olds, soon to be 3 year olds, or recently 
turned 4 year olds attending the selected practices. The study will 
gather feedback from parents/guardians about (1) their experiences 
receiving the book as part of a pediatric visit, and (2) the influence 
of the book on their awareness, attitudes, and self-efficacy regarding 
monitoring developmental milestones. Findings from the parent web 
survey and focus groups will help CDC to determine if a children's book 
is an effective channel for reaching parents, whether more books like 
Amazing Me for other age groups should be developed, and if the ROR 
book distribution model is an effective means to reach low-income and 
at-risk families.
    Data will be gathered through a web survey of 900 parents/guardians 
who have received a copy of the Amazing Me book from participating ROR 
and non-ROR practices. Parents/guardians will access the web survey by 
logging onto a URL address provided on a sticker affixed to the inside 
cover of each Amazing Me book. All survey responses (100%) will be 
submitted through a secure survey Web site established for this 
project.
    CDC will also conduct six follow-up focus groups with survey 
respondents to gather more in-depth information from parents about 
their experiences reading the Amazing Me book at home with their 
children and assessing their child's development using the book. We 
estimate that we will screen 60 parents/guardians to recruit 54 
participants for the focus groups. These six focus groups will be 
conducted in greater Atlanta, Georgia (2) and greater Washington, DC 
(4).
    This request is submitted to obtain OMB clearance for one year. The 
estimated annualized burden is 229 hours. There are no costs to the 
respondents other than their time.

[[Page 44569]]



                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                                      Average
                                                                     Number of       Number of      burden per
          Type of respondent                    Form name           respondents    responses per   response  (in
                                                                                    respondent        hours)
----------------------------------------------------------------------------------------------------------------
Parents/Guardians.....................  Web Survey..............             900               1           10/60
Parents/Guardians.....................  Follow-up web survey....             900               1            1/60
Parents/Guardians.....................  Focus Group Screener....              60               1            5/60
Parents/Guardians.....................  Focus Group Informed                  54               1            5/60
                                         Consent.
Parents/Guardians.....................  Focus Group Moderator...              54               1               1
----------------------------------------------------------------------------------------------------------------

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--

Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific 
Integrity, Office of the Associate Director for Science, Office of the 
Director, Centers for Disease Control and Prevention.
[FR Doc. 2013-17799 Filed 7-23-13; 8:45 am]
BILLING CODE 4163-18-P
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