Submission for OMB Review; 30-Day Comment Request, 46445-46446 [2014-18777]

Download as PDF Federal Register / Vol. 79, No. 153 / Friday, August 8, 2014 / Notices mstockstill on DSK4VPTVN1PROD with NOTICES Charter, presentations, and other meeting materials are located on the Advisory Committee’s Web site at https://www.hrsa.gov/advisory committees/mchbadvisory/heritable disorders. Public Comments: Members of the public may present oral comments and/ or submit written comments. Comments are part of the official Committee record. The public comment period is tentatively scheduled for September 11, 2014. Advance registration is required to present oral comments and/or submit written comments at https://www.bls meetings.net/ACHDNCSeptember2014/. The registration deadline is Thursday, August 28, 2014, 11:59 p.m. Eastern Time. Written comments must be received by the deadline in order to be included in the September meeting briefing book. Written comments should identify the individual’s name, address, email, telephone number, professional or business affiliation, type of expertise (i.e., parent, researcher, clinician, public health, etc.), and the topic/subject matter of comments. To ensure that all individuals who have registered to make oral comments can be accommodated, the allocated time may be limited. Individuals who are associated with groups or have similar interests may be requested to combine their comments and present them through a single representative. No audiovisual presentations are permitted. For additional information or questions on public comments, please contact Lisa Vasquez, Maternal and Child Health Bureau, Health Resources and Services Administration; email: lvasquez@ hrsa.gov. For More Information Contact: Anyone interested in obtaining other relevant information should contact Debi Sarkar, Maternal and Child Health Bureau, Health Resources and Services Administration, Room 18A–19, Parklawn Building, 5600 Fishers Lane, Rockville, Maryland 20857; email: dsarkar@hrsa.gov. More information on the Advisory Committee is available at https://www. hrsa.gov/advisorycommittees/mchb advisory/heritabledisorders. Dated: August 1, 2014. Jackie Painter, Acting Director, Division of Policy and Information Coordination. [FR Doc. 2014–18737 Filed 8–7–14; 8:45 am] BILLING CODE 4165–15–P VerDate Mar<15>2010 16:51 Aug 07, 2014 Jkt 232001 DEPARTMENT OF HEALTH AND HUMAN SERVICES Health Resources and Services Administration National Advisory Committee on Rural Health and Human Services; Notice of Meeting In accordance with section 10(a)(2) of the Federal Advisory Committee Act (Pub. L. 92–463), announcement is made of the following National Advisory body scheduled to meet during the month of September 2014. The National Advisory Committee on Rural Health and Human Services will convene its seventy sixth meeting in the time and place specified below: Name: National Advisory Committee on Rural Health and Human Services. Dates and Time: September 24, 2014, 8:45 a.m.–5:00 p.m. September 25, 2014, 8:30 a.m.–5:30 p.m. September 26, 2014, 8:30 a.m.–11:00 a.m. Place: Avera eHelm, 4500 N Lewis Ave, Sioux Falls, SD 57104, (605) 322– 4669. Status: The meeting will be open to the public. Purpose: The National Advisory Committee on Rural Health and Human Services provides counsel and recommendations to the Secretary with respect to the delivery, research, development, and administration of health and human services in rural areas. Agenda: Wednesday morning, at 8:45 a.m., the meeting will be called to order by the Chairperson of the Committee: The Honorable Ronnie Musgrove. The Committee will assess how telehealth coverage opportunities in rural areas are affected by the Affordable Care Act. The Committee will also examine the issue of rural domestic violence. The day will conclude with a period of public comment at approximately 4:45 p.m. Thursday morning at approximately 8:30 a.m., the Committee will break into Subcommittees and depart for site visits to health care and human services providers in South Dakota and Minnesota. Subcommittees will visit the Pipestone County Medical Center and the Good Samaritan Society in Pipestone, Minnesota, and the Horizon Health Clinic in Howard, South Dakota. The day will conclude at the Avera eHelm with a period of public comment at approximately 5:15 p.m. Friday morning at 8:30 a.m., the Committee will meet to summarize key findings and develop a work plan for the next quarter and the following meeting. FOR FURTHER INFORMATION CONTACT: Steve Hirsch, MSLS, Executive PO 00000 Frm 00051 Fmt 4703 Sfmt 4703 46445 Secretary, National Advisory Committee on Rural Health and Human Services, Health Resources and Services Administration, Parklawn Building, 17W29–C, 5600 Fishers Lane, Rockville, Maryland 20857, telephone (301) 443– 0835, or fax (301) 443–2803. Persons interested in attending any portion of the meeting should contact Catherine Fontenot at the Office of Rural Health Policy (ORHP) via telephone at (301) 945–0897or by email at cfontenot@ hrsa.gov. The Committee meeting agenda will be posted on the Committee’s Web site at https://www. hrsa.gov/advisorycommittees/rural/. Dated: August 1, 2014. Jackie Painter, Acting Director, Division of Policy and Information Coordination. [FR Doc. 2014–18735 Filed 8–7–14; 8:45 am] BILLING CODE 4165–15–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Submission for OMB Review; 30-Day Comment Request The Social Security Administration (SSA)—National Institutes of Health (NIH) Collaboration to Improve the Disability Determination Process: Calibration II, Predictive Validity Testing & Validation of Item Response Theory-Computer Adaptive Testing Tools (IRT–CAT) (CC) SUMMARY: Under the provisions of Section 3507(a)(1)(D) of the Paperwork Reduction Act of 1995, the National Institutes of Health (NIH) has submitted to the Office of Management and Budget (OMB) a request for review and approval of the information collection listed below. This proposed information collection was previously published in the Federal Register on April 22, 2014, page 22507 and allowed 60-days for public comment. No public comments were received. The purpose of this notice is to allow an additional 30 days for public comment. The Clinical Center, National Institutes of Health, may not conduct or sponsor, and the respondent is not required to respond to, an information collection that has been extended, revised, or implemented on or after October 1, 1995, unless it displays a currently valid OMB control number. Direct Comments to OMB: Written comments and/or suggestions regarding the item(s) contained in this notice, especially regarding the estimated public burden and associated response time, should be directed to the: Office E:\FR\FM\08AUN1.SGM 08AUN1 46446 Federal Register / Vol. 79, No. 153 / Friday, August 8, 2014 / Notices of Management and Budget, Office of Regulatory Affairs, OIRA_submission@ omb.eop.gov or by fax to 202–395–6974, Attention: NIH Desk Officer. DATES: Comment Due Date: Comments regarding this information collection are best assured of having their full effect if received within 30 days of the date of this publication. FOR FURTHER INFORMATION CONTACT: To obtain a copy of the data collection plans and instruments or request more information on the proposed project contact: Daniel Hobbs, Management Analyst, Epidemiology & Biostatistics Section, Rehabilitation Medicine Department, Clinical Center, NIH, 6100 Executive Blvd. Suite 3C01, Bethesda, MD 20892, or call non-toll-free number (301) 496–3817 or Email your request, including your address to: daniel.hobbs@nih.gov. Formal requests for additional plans and instruments must be requested in writing. Proposed Collection: The SSA–NIH Collaboration to Improve the Disability development of tests such as the Graduate Record Examination (GRE) and the Graduate Management Admission Test (GMAT). Development of these instruments is an iterative process, involving sequential phases of study in the areas of item bank development, calibration, validation, reliability testing and replenishment of the item banks. CAT instruments for the Applied Cognition and Activities of Daily Living domains will undergo calibration; predictive validity will be examined; concurrent validity will be tested against legacy functional assessment instruments; reliability and sensitivity will be examined; and, the item banks will undergo replenishment to refine the scope of the questions. OMB approval is requested for 3 years. There are no costs to respondents other than their time. The total estimated annualized burden hours are 12,835. Determination Process: Calibration II, Predictive Validity Testing & Validation of IRT–CAT Tools, 0925– New, Clinical Center (CC), National Institutes of Health (NIH). Need and Use of Information Collection: The Social Security Administration (SSA) entered into an interagency agreement (IAA) with the National Institutes of Health (NIH), Clinical Center (CC), Rehabilitation Medicine Department (RMD), to explore innovative methods of functional assessment to improve SSA’s disability determination process. As part of its study, NIH recommended item response theory (IRT) coupled with computer adaptive testing (CAT) as a promising approach to efficiently and consistently capture claimant functional information to assist SSA adjudicators. IRT is a framework for the design, analysis, and scoring of tests, questionnaires, and similar instruments measuring abilities, aptitudes, and other variables. It is often the preferred method for the ESTIMATED ANNUALIZED BURDEN HOURS Type of respondents Number of respondents Frequency of response Average time per response (in hours) Annual hour burden Calibration Phase Survey 1—Screener Call (Not Interested) ....................................................... Survey 1—Screener Call (Participate/Eligible) ................................................ Survey 1—Consent Form ................................................................................ SSA Claimant Survey 1 ................................................................................... Survey 2—Screener Call (Not Interested) ....................................................... Survey 2—Screener Call (Participate Eligible) ................................................ Survey 2—Consent Form ................................................................................ SSA Claimant Survey 2 ................................................................................... Normative Population Survey 1 ....................................................................... Normative Population Survey 2 ....................................................................... Dated: July 31, 2014. David Henderson, Deputy Director, Clinical Center, NIH. BILLING CODE 4140–01–P DEPARTMENT OF HOMELAND SECURITY U.S. Citizenship and Immigration Services mstockstill on DSK4VPTVN1PROD with NOTICES [OMB Control Number 1615–0049] Agency Information Collection Activities: Request for Verification of Naturalization, Form N–25; Extension, Without Change, of a Currently Approved Collection ACTION: 60-Day Notice. VerDate Mar<15>2010 16:51 Aug 07, 2014 Jkt 232001 The Department of Homeland Security (DHS), U.S. Citizenship and Immigration Services (USCIS) invites the general public and other Federal agencies to comment upon this proposed extension of a currently approved collection of information. In accordance with the Paperwork Reduction Act (PRA) of 1995, the information collection notice is published in the Federal Register to obtain comments regarding the nature of the information collection, the categories of respondents, the estimated burden (i.e. the time, effort, and resources used by the respondents to respond), the estimated cost to the respondent, and the actual information collection instruments. DATES: Comments are encouraged and will be accepted for 60 days until October 7, 2014. SUMMARY: [FR Doc. 2014–18777 Filed 8–7–14; 8:45 am] 12,200 7,800 3,500 3,500 500 3,000 3,000 3,000 2,000 2,000 PO 00000 Frm 00052 Fmt 4703 Sfmt 4703 1 1 1 1 1 1 1 1 1 1 3/60 15/60 15/60 45/60 3/60 15/60 15/60 45/60 45/60 45/60 610 1,950 875 2,625 25 750 750 2,250 1,500 1,500 All submissions received must include the OMB Control Number 1615–0049 in the subject box, the agency name and Docket ID USCIS– 2005–0036. To avoid duplicate submissions, please use only one of the following methods to submit comments: (1) Online. Submit comments via the Federal eRulemaking Portal Web site at www.regulations.gov under e-Docket ID number USCIS–2005–0036; (2) Email. Submit comments to USCISFRComment@uscis.dhs.gov; (3) Mail. Submit written comments to DHS, USCIS, Office of Policy and Strategy, Chief, Regulatory Coordination Division, 20 Massachusetts Avenue NW., Washington, DC 20529–2140. ADDRESSES: SUPPLEMENTARY INFORMATION: E:\FR\FM\08AUN1.SGM 08AUN1

Agencies

[Federal Register Volume 79, Number 153 (Friday, August 8, 2014)]
[Notices]
[Pages 46445-46446]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-18777]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Submission for OMB Review; 30-Day Comment Request

The Social Security Administration (SSA)--National Institutes of Health 
(NIH) Collaboration to Improve the Disability Determination Process: 
Calibration II, Predictive Validity Testing & Validation of Item 
Response Theory-Computer Adaptive Testing Tools (IRT-CAT) (CC)
SUMMARY: Under the provisions of Section 3507(a)(1)(D) of the Paperwork 
Reduction Act of 1995, the National Institutes of Health (NIH) has 
submitted to the Office of Management and Budget (OMB) a request for 
review and approval of the information collection listed below. This 
proposed information collection was previously published in the Federal 
Register on April 22, 2014, page 22507 and allowed 60-days for public 
comment. No public comments were received. The purpose of this notice 
is to allow an additional 30 days for public comment. The Clinical 
Center, National Institutes of Health, may not conduct or sponsor, and 
the respondent is not required to respond to, an information collection 
that has been extended, revised, or implemented on or after October 1, 
1995, unless it displays a currently valid OMB control number.
    Direct Comments to OMB: Written comments and/or suggestions 
regarding the item(s) contained in this notice, especially regarding 
the estimated public burden and associated response time, should be 
directed to the: Office

[[Page 46446]]

of Management and Budget, Office of Regulatory Affairs, OIRA_submission@omb.eop.gov or by fax to 202-395-6974, Attention: NIH Desk 
Officer.

DATES: Comment Due Date: Comments regarding this information collection 
are best assured of having their full effect if received within 30 days 
of the date of this publication.

FOR FURTHER INFORMATION CONTACT: To obtain a copy of the data 
collection plans and instruments or request more information on the 
proposed project contact: Daniel Hobbs, Management Analyst, 
Epidemiology & Biostatistics Section, Rehabilitation Medicine 
Department, Clinical Center, NIH, 6100 Executive Blvd. Suite 3C01, 
Bethesda, MD 20892, or call non-toll-free number (301) 496-3817 or 
Email your request, including your address to: daniel.hobbs@nih.gov. 
Formal requests for additional plans and instruments must be requested 
in writing.
    Proposed Collection: The SSA-NIH Collaboration to Improve the 
Disability Determination Process: Calibration II, Predictive Validity 
Testing & Validation of IRT-CAT Tools, 0925- New, Clinical Center (CC), 
National Institutes of Health (NIH).
    Need and Use of Information Collection: The Social Security 
Administration (SSA) entered into an interagency agreement (IAA) with 
the National Institutes of Health (NIH), Clinical Center (CC), 
Rehabilitation Medicine Department (RMD), to explore innovative methods 
of functional assessment to improve SSA's disability determination 
process. As part of its study, NIH recommended item response theory 
(IRT) coupled with computer adaptive testing (CAT) as a promising 
approach to efficiently and consistently capture claimant functional 
information to assist SSA adjudicators. IRT is a framework for the 
design, analysis, and scoring of tests, questionnaires, and similar 
instruments measuring abilities, aptitudes, and other variables. It is 
often the preferred method for the development of tests such as the 
Graduate Record Examination (GRE) and the Graduate Management Admission 
Test (GMAT).
    Development of these instruments is an iterative process, involving 
sequential phases of study in the areas of item bank development, 
calibration, validation, reliability testing and replenishment of the 
item banks. CAT instruments for the Applied Cognition and Activities of 
Daily Living domains will undergo calibration; predictive validity will 
be examined; concurrent validity will be tested against legacy 
functional assessment instruments; reliability and sensitivity will be 
examined; and, the item banks will undergo replenishment to refine the 
scope of the questions.
    OMB approval is requested for 3 years. There are no costs to 
respondents other than their time. The total estimated annualized 
burden hours are 12,835.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                   Average time
               Type of respondents                   Number of     Frequency of    per response     Annual hour
                                                    respondents      response       (in hours)        burden
----------------------------------------------------------------------------------------------------------------
                                                Calibration Phase
----------------------------------------------------------------------------------------------------------------
Survey 1--Screener Call (Not Interested)........          12,200               1            3/60             610
Survey 1--Screener Call (Participate/Eligible)..           7,800               1           15/60           1,950
Survey 1--Consent Form..........................           3,500               1           15/60             875
SSA Claimant Survey 1...........................           3,500               1           45/60           2,625
Survey 2--Screener Call (Not Interested)........             500               1            3/60              25
Survey 2--Screener Call (Participate Eligible)..           3,000               1           15/60             750
Survey 2--Consent Form..........................           3,000               1           15/60             750
SSA Claimant Survey 2...........................           3,000               1           45/60           2,250
Normative Population Survey 1...................           2,000               1           45/60           1,500
Normative Population Survey 2...................           2,000               1           45/60           1,500
----------------------------------------------------------------------------------------------------------------


    Dated: July 31, 2014.
David Henderson,
Deputy Director, Clinical Center, NIH.
[FR Doc. 2014-18777 Filed 8-7-14; 8:45 am]
BILLING CODE 4140-01-P
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