83_FR_2172 83 FR 2162 - Proposed Information Collection Activity; Comment Request; Job Search Assistance (JSA) Strategies Evaluation-Extension

83 FR 2162 - Proposed Information Collection Activity; Comment Request; Job Search Assistance (JSA) Strategies Evaluation-Extension

DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families

Federal Register Volume 83, Issue 10 (January 16, 2018)

Page Range2162-2163
FR Document2018-00612

Federal Register, Volume 83 Issue 10 (Tuesday, January 16, 2018)
[Federal Register Volume 83, Number 10 (Tuesday, January 16, 2018)]
[Notices]
[Pages 2162-2163]
From the Federal Register Online  [www.thefederalregister.org]
[FR Doc No: 2018-00612]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families

[OMB NO.: 0970-0440]


Proposed Information Collection Activity; Comment Request; Job 
Search Assistance (JSA) Strategies Evaluation--Extension

    Description: The Administration for Children and Families (ACF), is 
proposing the extension without changes to an existing data collection 
activity as part of the Job Search Assistance (JSA) Strategies 
Evaluation. The JSA evaluation will aim to determine which JSA 
strategies are most effective in moving TANF applicants and recipients 
into work and will produce impact and implementation findings. To date, 
the study has randomly assigned individuals to contrasting JSA 
approaches. The study will next compare participant employment and 
earnings to determine the relative effectiveness of these strategies. 
The project will also report on the implementation of these strategies, 
including measures of services participants receive under each 
approach, as well as provide operational lessons gathered directly from 
practitioners.
    Data collection efforts previously approved for JSA, include: Data 
collection activities to document program implementation, a staff 
survey, a baseline information form for program participants, and a 
follow-up survey for JSA participants approximately 6 months after 
program enrollment. Approval for these activities expires on February 
28, 2018.
    This Federal Register Notice provides the opportunity to comment on 
the extension of the 6-month follow-up survey to allow follow-up data 
to be collected for all study participants. Although the enrollment 
period was originally estimated to span 12 months, it took 18 months to 
complete enrollment, leaving insufficient time to complete the 6-month 
follow-up survey. A four-month extension is requested in order to allow 
individuals randomly assigned between June and August 2017 to complete 
the follow-up survey in the same timeframe as earlier enrollees. The 
purpose of the survey is to follow-up with study participants and 
document their job search assistance services and experiences including 
their receipt of job search assistance services, their knowledge and 
skills for conducting a job search, the nature of their job search 
process, including tools and services used to locate employment, and 
their search outputs and outcomes, such as the number of applications 
submitted, interviews attended, offers received and jobs obtained. In 
addition, the survey will provide an opportunity for respondents to 
provide contact data for possible longer-term follow-up. There are no 
changes to the currently approved instruments.
    Respondents: JSA study participants.

Annual Burden Estimates

    This extension is specific to the 6-month survey and covers the 
remaining 766 participants that may be completing the six-month follow 
up survey during the four-month extension period. All other information 
collection under 0970-0440 will be complete by the original OMB 
expiration date of February 28, 2018.

[[Page 2163]]



----------------------------------------------------------------------------------------------------------------
                                                Total/annual      Number of      Average burden
                 Instrument                      number of      responses per      hours per      Annual burden
                                                respondents       respondent        response          hours
----------------------------------------------------------------------------------------------------------------
                             Extension of Previously Approved Information Collection
----------------------------------------------------------------------------------------------------------------
6-Month Follow-Up Survey....................             766                1             .333              255
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 255.
    In compliance with the requirements of Section 3506(c)(2)(A) of the 
Paperwork Reduction Act of 1995, the Administration for Children and 
Families is soliciting public comment on the specific aspects of the 
information collection described above. Copies of the proposed 
collection of information can be obtained and comments may be forwarded 
by writing to the Administration for Children and Families, Office of 
Planning, Research, and Evaluation, 330 C Street SW, Washington, DC 
20201, Attn: OPRE Reports Clearance Officer. Email address: 
[email protected]. All requests should be identified by 
the title of the information collection.
    The Department specifically requests comments on (a) whether the 
proposed collection of information is necessary for the proper 
performance of the functions of the agency, including whether the 
information shall have practical utility; (b) the accuracy of the 
agency's estimate of the burden of the proposed collection of 
information; (c) the quality, utility, and clarity of the information 
to be collected; and (d) ways to minimize the burden of the collection 
of information on respondents, including through the use of automated 
collection techniques or other forms of information technology. 
Consideration will be given to comments and suggestions submitted 
within 60 days of this publication.

Mary Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2018-00612 Filed 1-12-18; 8:45 am]
 BILLING CODE 4184-09-P



                                               2162                          Federal Register / Vol. 83, No. 10 / Tuesday, January 16, 2018 / Notices

                                               DATES:  Comments on the collection(s) of                Health Insurance Portability and                       contrasting JSA approaches. The study
                                               information must be received by the                     Accountability Act (HIPAA) Privacy                     will next compare participant
                                               OMB desk officer by February 15, 2018.                  Rule (§ 164.508) prohibits Medicare (a                 employment and earnings to determine
                                               ADDRESSES: When commenting on the                       HIPAA covered entity) from disclosing                  the relative effectiveness of these
                                               proposed information collections,                       an individual’s protected health                       strategies. The project will also report
                                               please reference the document identifier                information without a valid                            on the implementation of these
                                               or OMB control number. To be assured                    authorization. In order to be valid, an                strategies, including measures of
                                               consideration, comments and                             authorization must include specified                   services participants receive under each
                                               recommendations must be received by                     core elements and statements. Medicare                 approach, as well as provide operational
                                               the OMB desk officer via one of the                     will make available to Medicare                        lessons gathered directly from
                                               following transmissions: OMB, Office of                 beneficiaries a standard, valid                        practitioners.
                                               Information and Regulatory Affairs,                     authorization to enable beneficiaries to                  Data collection efforts previously
                                               Attention: CMS Desk Officer, Fax                        request the disclosure of their protected              approved for JSA, include: Data
                                               Number: (202) 395–5806 OR, Email:                       health information. This standard                      collection activities to document
                                               OIRA_submission@omb.eop.gov.                            authorization will simplify the process                program implementation, a staff survey,
                                                 To obtain copies of a supporting                      of requesting information disclosure for               a baseline information form for program
                                               statement and any related forms for the                 beneficiaries and minimize the response                participants, and a follow-up survey for
                                               proposed collection(s) summarized in                    time for Medicare. Form CMS–10106,                     JSA participants approximately 6
                                               this notice, you may make your request                  the Medicare Authorization to Disclose                 months after program enrollment.
                                               using one of following:                                 Personal Health Information, will be                   Approval for these activities expires on
                                                 1. Access CMS’ website address at                     used by Medicare beneficiaries to                      February 28, 2018.
                                               website address at https://www.cms.gov/                 authorize Medicare to disclose their                      This Federal Register Notice provides
                                               Regulations-and-Guidance/Legislation/                   protected health information to a third                the opportunity to comment on the
                                               PaperworkReductionActof1995/PRA-                        party. Form Number: CMS–10106 (OMB                     extension of the 6-month follow-up
                                               Listing.html.                                           control number: 0938–0930); Frequency:                 survey to allow follow-up data to be
                                                 2. Email your request, including your                 Occasionally; Affected Public:                         collected for all study participants.
                                               address, phone number, OMB number,                      Individuals or Households; Number of                   Although the enrollment period was
                                               and CMS document identifier, to                         Respondents: 2,200,000; Total Annual                   originally estimated to span 12 months,
                                               Paperwork@cms.hhs.gov.                                  Responses: 2,200,000; Total Annual                     it took 18 months to complete
                                                 3. Call the Reports Clearance Office at               Hours: 550,000. (For policy questions                  enrollment, leaving insufficient time to
                                               (410) 786–1326.                                         regarding this collection contact Sam                  complete the 6-month follow-up survey.
                                               FOR FURTHER INFORMATION CONTACT:                        Jenkins at 410–786–3261.)                              A four-month extension is requested in
                                               William Parham at (410) 786–4669.                          Dated: January 9, 2018.                             order to allow individuals randomly
                                               SUPPLEMENTARY INFORMATION: Under the                    William N. Parham, III,                                assigned between June and August 2017
                                               Paperwork Reduction Act of 1995 (PRA)                   Director, Paperwork Reduction Staff, Office            to complete the follow-up survey in the
                                               (44 U.S.C. 3501–3520), federal agencies                 of Strategic Operations and Regulatory                 same timeframe as earlier enrollees. The
                                               must obtain approval from the Office of                 Affairs.                                               purpose of the survey is to follow-up
                                               Management and Budget (OMB) for each                    [FR Doc. 2018–00486 Filed 1–12–18; 8:45 am]            with study participants and document
                                               collection of information they conduct                  BILLING CODE 4120–01–P
                                                                                                                                                              their job search assistance services and
                                               or sponsor. The term ‘‘collection of                                                                           experiences including their receipt of
                                               information’’ is defined in 44 U.S.C.                                                                          job search assistance services, their
                                               3502(3) and 5 CFR 1320.3(c) and                         DEPARTMENT OF HEALTH AND                               knowledge and skills for conducting a
                                               includes agency requests or                             HUMAN SERVICES                                         job search, the nature of their job search
                                               requirements that members of the public                                                                        process, including tools and services
                                               submit reports, keep records, or provide                Administration for Children and                        used to locate employment, and their
                                               information to a third party. Section                   Families                                               search outputs and outcomes, such as
                                               3506(c)(2)(A) of the PRA (44 U.S.C.                                                                            the number of applications submitted,
                                                                                                       [OMB NO.: 0970–0440]
                                               3506(c)(2)(A)) requires federal agencies                                                                       interviews attended, offers received and
                                               to publish a 30-day notice in the                       Proposed Information Collection                        jobs obtained. In addition, the survey
                                               Federal Register concerning each                        Activity; Comment Request; Job                         will provide an opportunity for
                                               proposed collection of information,                     Search Assistance (JSA) Strategies                     respondents to provide contact data for
                                               including each proposed extension or                    Evaluation—Extension                                   possible longer-term follow-up. There
                                               reinstatement of an existing collection                                                                        are no changes to the currently
                                               of information, before submitting the                      Description: The Administration for                 approved instruments.
                                               collection to OMB for approval. To                      Children and Families (ACF), is                           Respondents: JSA study participants.
                                               comply with this requirement, CMS is                    proposing the extension without
                                                                                                                                                              Annual Burden Estimates
                                               publishing this notice that summarizes                  changes to an existing data collection
                                               the following proposed collection(s) of                 activity as part of the Job Search                       This extension is specific to the 6-
                                               information for public comment:                         Assistance (JSA) Strategies Evaluation.                month survey and covers the remaining
                                                 1. Type of Information Collection                     The JSA evaluation will aim to                         766 participants that may be completing
                                               Request: Reinstatement without change                   determine which JSA strategies are most                the six-month follow up survey during
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                                               of a previously approved collection;                    effective in moving TANF applicants                    the four-month extension period. All
                                               Title of Information Collection:                        and recipients into work and will                      other information collection under
                                               Medicare Authorization to Disclose                      produce impact and implementation                      0970–0440 will be complete by the
                                               Personal Health Information; Use:                       findings. To date, the study has                       original OMB expiration date of
                                               Unless permitted or required by law, the                randomly assigned individuals to                       February 28, 2018.




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                                                                                  Federal Register / Vol. 83, No. 10 / Tuesday, January 16, 2018 / Notices                                                         2163

                                                                                                                                                                          Number of re-
                                                                                                                                                          Total/annual                          Average
                                                                                                                                                                            sponses                             Annual
                                                                                           Instrument                                                        number                           burden hours
                                                                                                                                                                          per respond-                       burden hours
                                                                                                                                                         of respondents                       per response
                                                                                                                                                                               ent

                                                                                                        Extension of Previously Approved Information Collection

                                               6-Month Follow-Up Survey ..............................................................................         766               1                .333           255



                                                 Estimated Total Annual Burden                                   DEPARTMENT OF HEALTH AND                                    1997 (FDAMA) (Pub. L. 105–115)
                                               Hours: 255.                                                       HUMAN SERVICES                                              became effective on February 19, 1998.
                                                 In compliance with the requirements                                                                                         FDAMA amended the previous medical
                                                                                                                 Food and Drug Administration                                device tracking provisions under section
                                               of Section 3506(c)(2)(A) of the
                                               Paperwork Reduction Act of 1995, the                              [Docket No. FDA–2017–N–5569]                                519(e)(1) and (2) of the Federal Food,
                                                                                                                                                                             Drug, and Cosmetic Act (FD&C Act) (21
                                               Administration for Children and
                                                                                                                 Agency Information Collection                               U.S.C. 360i(e)(1) and (2)) that were
                                               Families is soliciting public comment
                                                                                                                 Activities; Submission for Office of                        added by the Safe Medical Devices Act
                                               on the specific aspects of the                                                                                                of 1990 (SMDA) (Pub. L. 101–629).
                                                                                                                 Management and Budget Review;
                                               information collection described above.                                                                                       Unlike the tracking provisions under
                                                                                                                 Comment Request; Medical Devices;
                                               Copies of the proposed collection of                                                                                          SMDA, which required tracking of any
                                                                                                                 Device Tracking
                                               information can be obtained and                                                                                               medical device meeting certain criteria,
                                               comments may be forwarded by writing                              AGENCY:       Food and Drug Administration,                 FDAMA allows FDA discretion in
                                               to the Administration for Children and                            HHS.                                                        applying tracking provisions to medical
                                               Families, Office of Planning, Research,                           ACTION:      Notice.                                        devices meeting certain criteria and
                                               and Evaluation, 330 C Street SW,                                                                                              provides that tracking requirements for
                                               Washington, DC 20201, Attn: OPRE                                  SUMMARY:   The Food and Drug
                                                                                                                                                                             medical devices can be imposed only
                                               Reports Clearance Officer. Email                                  Administration (FDA) is announcing
                                                                                                                                                                             after FDA issues an order. In the Federal
                                                                                                                 that a proposed collection of
                                               address: OPREinfocollection@                                                                                                  Register of February 8, 2002 (67 FR
                                                                                                                 information has been submitted to the
                                               acf.hhs.gov. All requests should be                                                                                           5943), FDA issued a final rule that
                                                                                                                 Office of Management and Budget
                                               identified by the title of the information                                                                                    conformed existing tracking regulations
                                                                                                                 (OMB) for review and clearance under
                                               collection.                                                                                                                   to changes in tracking provisions
                                                                                                                 the Paperwork Reduction Act of 1995.
                                                 The Department specifically requests                                                                                        effected by FDAMA under part 821 (21
                                                                                                                 DATES: Fax written comments on the                          CFR part 821).
                                               comments on (a) whether the proposed                              collection of information by February                          Section 519(e)(1) of the FD&C Act, as
                                               collection of information is necessary                            15, 2018.                                                   amended by FDAMA, provides that
                                               for the proper performance of the                                 ADDRESSES: To ensure that comments on                       FDA may require by order that a
                                               functions of the agency, including                                the information collection are received,                    manufacturer adopt a method for
                                               whether the information shall have                                OMB recommends that written                                 tracking a class II or III medical device,
                                               practical utility; (b) the accuracy of the                        comments be faxed to the Office of                          if the device meets one of the three
                                               agency’s estimate of the burden of the                            Information and Regulatory Affairs,                         following criteria: (1) The failure of the
                                               proposed collection of information; (c)                           OMB, Attn: FDA Desk Officer, Fax: 202–                      device would be reasonably likely to
                                               the quality, utility, and clarity of the                          395–7285, or emailed to oira_                               have serious adverse health
                                               information to be collected; and (d)                              submission@omb.eop.gov. All                                 consequences, (2) the device is intended
                                               ways to minimize the burden of the                                comments should be identified with the                      to be implanted in the human body for
                                               collection of information on                                      OMB control number 0910–0442. Also                          more than 1 year (referred to as a
                                               respondents, including through the use                            include the FDA docket number found                         ‘‘tracked implant’’), or (3) the device is
                                               of automated collection techniques or                             in brackets in the heading of this                          life-sustaining or life-supporting
                                               other forms of information technology.                            document.                                                   (referred to as a ‘‘tracked l/s-l/s device’’)
                                               Consideration will be given to                                    FOR FURTHER INFORMATION CONTACT:                            and is used outside a device user
                                               comments and suggestions submitted                                Amber Sanford, Office of Operations,                        facility.
                                               within 60 days of this publication.                               Food and Drug Administration, Three                            Tracked device information is
                                                                                                                 White Flint North, 10A–12M, 11601                           collected to facilitate identifying the
                                               Mary Jones,                                                                                                                   current location of medical devices and
                                                                                                                 Landsdown St., North Bethesda, MD
                                               ACF/OPRE Certifying Officer.                                      20852, 301–796–8867, PRAStaff@                              patients possessing those devices, to the
                                               [FR Doc. 2018–00612 Filed 1–12–18; 8:45 am]                       fda.hhs.gov.                                                extent that patients permit the
                                               BILLING CODE 4184–09–P                                                                                                        collection of identifying information.
                                                                                                                 SUPPLEMENTARY INFORMATION:    In                            Manufacturers and FDA (where
                                                                                                                 compliance with 44 U.S.C. 3507, FDA                         necessary) use the data to: (1) Expedite
                                                                                                                 has submitted the following proposed                        the recall of distributed medical devices
                                                                                                                 collection of information to OMB for                        that are dangerous or defective and (2)
                                                                                                                 review and clearance.                                       facilitate the timely notification of
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                                                                                                                 Medical Devices; Device Tracking—21                         patients or licensed practitioners of the
                                                                                                                 CFR Part 821                                                risks associated with the medical
                                                                                                                                                                             device.
                                                                                                                 OMB Control Number 0910–0442—                                  In addition, the regulations include
                                                                                                                 Extension                                                   provisions for: (1) Exemptions and
                                                                                                                   Section 211 of the Food and Drug                          variances; (2) system and content
                                                                                                                 Administration Modernization Act of                         requirements for tracking; (3)


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Document Created: 2018-01-13 02:02:45
Document Modified: 2018-01-13 02:02:45
CategoryRegulatory Information
CollectionFederal Register
sudoc ClassAE 2.7:
GS 4.107:
AE 2.106:
PublisherOffice of the Federal Register, National Archives and Records Administration
SectionNotices
FR Citation83 FR 2162 

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