Agency Information Collection Activities: Submission for OMB Review; Comment Request, 63931-63932 [2011-26590]

Download as PDF 63931 Federal Register / Vol. 76, No. 199 / Friday, October 14, 2011 / Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES Health Resources and Services Administration Agency Information Collection Activities: Submission for OMB Review; Comment Request Periodically, the Health Resources and Services Administration (HRSA) publishes abstracts of information collection requests under review by the Office of Management and Budget (OMB), in compliance with the Paperwork Reduction Act of 1995 (44 U.S.C. chapter 35). To request a copy of the clearance requests submitted to OMB for review, e-mail paperwork@hrsa.gov or call the HRSA Reports Clearance Office at (301) 443– 1129. The following request has been submitted to the Office of Management and Budget for review under the Paperwork Reduction Act of 1995: Proposed Project Title: Evaluation of the Text4baby Program—(OMB No. 0915–xxxx)—[NEW] Background: Text4baby is a mobile health education program that provides free, brief, evidence-based, health messages to women who are pregnant or have an infant under one year of age. An educational program led by the National Healthy Mothers, Healthy Babies coalition (HMHB), Text4baby is Instrument Consent Training and Coordination. Prenatal Patient Consent .... Parent-of-Minor Consent ..... intended to help women have safe and healthy pregnancies by empowering them with information they need to give their babies the best possible start in life. The Text4baby program was launched nationally in February 2010. Text4baby is made possible through a broad, public-private partnership that includes government and Tribal agencies, corporations, academic institutions, professional associations, and non-profit organizations. The goal of this program evaluation is to examine the characteristics of women who utilize the Text4baby mobile phone-based program, to assess their experience with the program, and to determine whether enrollment in Text4baby is associated with healthy behaviors and timely access to health care during pregnancy and an infant’s first year of life. This information will help the Department of Health and Human Services understand the usefulness of mobile health technology and the potential for expanding and/or adapting mobile phone messaging to additional health topics or conditions. The study also may offer insight into planning and implementing similar projects. Purpose: The purpose of the evaluation is to assess the usefulness of the Text4baby program. The four data collection components are as follows: • Safety Consumer Net Survey with subscribers and non-subscribers to the Text4baby program who receive Responses per respondent Number of respondents Person incurring burden prenatal care in community health centers in four communities. The health centers will recruit eligible women, obtain their signed consent to participate in the study, and convey their contact information to the data collection contractor. Data from the telephone survey will be linked to selected data from electronic health records (EHRs) for respondents who consent to the release of their EHRs. The survey will be conducted in two rounds: Round 1 will include pregnant women and Round 2 will include the same women approximately nine months later during the postpartum period. • Focus Groups with current subscribers in four communities to obtain more in-depth qualitative data regarding the usefulness of the messages and the program. • Key Informant Interviews of a diverse mix of providers in four communities to obtain provider perspectives on the usefulness of the Text4baby programs. Providers could include physicians, midwives, nurses, case managers, outreach workers, and health educators. • Stakeholder Interviews with Text4baby partners (public and private) to examine the implementation of Text4baby at the national, regional, state, or local level, including outreach, enrollment, coalition building, sustainability, and replication. The annual estimate of burden is as follows: Total responses Hours per response Total burden hours Health Center Study Coordinators. Health Center Staff ............ Health Center Staff ............ Prenatal Patient .................. Health Center Staff ............ Parent of Minor .................. Prenatal Patient .................. 8 12 96 1.00 96 32 1630 1630 195 195 960 1 1 1 1 1 1 32 1630 1630 195 195 960 1.00 0.08 0.08 0.25 0.08 0.33 32 130 130 49 16 317 Postpartum Patient ............. 768 1 768 0.33 253 Prenatal/Postpartum Patient Providers ............................ Stakeholders ...................... 80 40 30 1 1 1 80 40 30 1.50 0.75 0.75 120 30 23 Total ............................. tkelley on DSK3SPTVN1PROD with NOTICES Safety Net Consumer Survey Round 1. Safety Net Consumer Survey Round 2. Focus Groups ..................... Key Informant Interviews .... Stakeholder Interviews ........ ............................................. ........................ ........................ ........................ ........................ 1196 VerDate Mar<15>2010 15:20 Oct 13, 2011 Jkt 226001 PO 00000 Frm 00031 Fmt 4703 Sfmt 9990 E:\FR\FM\14OCN1.SGM 14OCN1 63932 Federal Register / Vol. 76, No. 199 / Friday, October 14, 2011 / Notices Written comments and recommendations concerning the proposed information collection should be sent within 30 days of this notice to the desk officer for HRSA, either by email to OIRA_submission@omb.eop.gov or by fax to 202–395–6974. Please direct all correspondence to the ‘‘attention of the desk officer for HRSA.’’ Dated: October 7, 2011. Reva Harris, Acting Director, Division of Policy and Information Coordination. [FR Doc. 2011–26590 Filed 10–13–11; 8:45 am] BILLING CODE 4165–15–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Human Genome Research Institute; Notice of Closed Meeting Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of the following meeting. The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. tkelley on DSK3SPTVN1PROD with NOTICES Name of Committee: National Human Genome Research Institute Special Emphasis Panel, ENCODE Technology RFA–SEP. Date: November 29, 2011. Time: 8 a.m. to 5 p.m. Agenda: To review and evaluate grant applications. Place: Residence Inn Bethesda, 7335 Wisconsin Avenue, Bethesda, MD 20814. Contact Person: Keith McKenney, PhD, Scientific Review Officer, NHGRI, 5635 Fishers Lane, Suite 4076, Bethesda, MD 20814, 301–594–4280, mckenneyk@mail.nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.172, Human Genome Research, National Institutes of Health, HHS) Dated: October 7, 2011 . Jennifer S. Spaeth, Director, Office of Federal Advisory Committee Policy. [FR Doc. 2011–26617 Filed 10–13–11; 8:45 am] BILLING CODE 4140–01–P VerDate Mar<15>2010 15:20 Oct 13, 2011 Jkt 226001 DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute of Diabetes and Digestive and Kidney Diseases; Notice of Closed Meetings Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of the following meetings. The meetings will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: National Institute of Diabetes and Digestive and Kidney Diseases Special Emphasis Panel, NIDDK Ancillary RO1 Telephone Review SEP. Date: November 14, 2011. Time: 1 p.m. to 2:30 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, Two Democracy Plaza, 6707 Democracy Boulevard, Bethesda, MD 20892, (Telephone Conference Call). Contact Person: Xiaodu Guo, M.D., PhD, Scientific Review Officer, Review Branch, DEA, NIDDK, National Institutes of Health, Room 761, 6707 Democracy Boulevard, Bethesda, MD 20892–5452, (301) 594–4719, guox@extra.niddk.nih.gov. Name of Committee: National Institute of Diabetes and Digestive and Kidney Diseases Special Emphasis Panel, NIDDK PO1 Telephone Review SEP. Date: November 29, 2011. Time: 1 p.m. to 3 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, Two Democracy Plaza, 6707 Democracy Boulevard, Bethesda, MD 20892, (Telephone Conference Call). Contact Person: Xiaodu Guo, M.D., PhD, Scientific Review Officer, Review Branch, DEA, NIDDK, National Institutes of Health, Room 761, 6707 Democracy Boulevard, Bethesda, MD 20892–5452, (301) 594–4719, guox@extra.niddk.nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.847, Diabetes, Endocrinology and Metabolic Research; 93.848, Digestive Diseases and Nutrition Research; 93.849, Kidney Diseases, Urology and Hematology Research, National Institutes of Health, HHS) PO 00000 Frm 00032 Fmt 4703 Sfmt 4703 Dated: October 7, 2011. Jennifer S. Spaeth, Director, Office of Federal Advisory Committee Policy. [FR Doc. 2011–26620 Filed 10–13–11; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Eunice Kennedy Shriver National Institute of Child Health & Human Development; Notice of Meeting Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of a meeting of the Board of Scientific Counselors, NICHD. The meeting will be open to the public as indicated below, with the attendance limited to space available. Individuals who plan to attend and need special assistance, such as sign language interpretation or other reasonable accommodations, should notify the Contact Person listed below in advance of the meeting. The meeting will be closed to the public as indicated below in accordance with the provisions set forth in section 552b(c)(6), Title 5 U.S.C., as amended for the review, discussion, and evaluation of individual intramural programs and projects conducted by the Eunice Kennedy Shriver National Institute of Child Health & Human Development, including consideration of personnel qualifications and performance, and the competence of individual investigators, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: Board of Scientific Counselors, NICHD. Date: December 2, 2011. Open: 8 a.m. to 11:30 a.m. Agenda: A report by the Scientific Director, NICHD, on the status of the NICHD Division of Intramural Research. Place: National Institutes of Health, Building 31, 9000 Rockville Pike, Room 2A48, Bethesda, MD 20892. Closed: 11:30 a.m. to 4 p.m. Agenda: To review and evaluate personal qualifications and performance, and competence of individual investigators. Place: National Institutes of Health, Building 31, 9000 Rockville Pike, Room 2A48, Bethesda, MD 20892. Contact Person: Constantine A. Stratakis, MD, D(med)Sci, Scientific Director, Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, 9000 Rockville Pike, Building 31, Room 2A46, Bethesda, MD 20892, 301–594–5984, stratakc@mail.nih.gov. E:\FR\FM\14OCN1.SGM 14OCN1

Agencies

[Federal Register Volume 76, Number 199 (Friday, October 14, 2011)]
[Notices]
[Pages 63931-63932]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-26590]



[[Page 63931]]

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Health Resources and Services Administration


Agency Information Collection Activities: Submission for OMB 
Review; Comment Request

    Periodically, the Health Resources and Services Administration 
(HRSA) publishes abstracts of information collection requests under 
review by the Office of Management and Budget (OMB), in compliance with 
the Paperwork Reduction Act of 1995 (44 U.S.C. chapter 35). To request 
a copy of the clearance requests submitted to OMB for review, e-mail 
paperwork@hrsa.gov or call the HRSA Reports Clearance Office at (301) 
443-1129.
    The following request has been submitted to the Office of 
Management and Budget for review under the Paperwork Reduction Act of 
1995:

Proposed Project Title: Evaluation of the Text4baby Program--(OMB No. 
0915-xxxx)--[NEW]

    Background: Text4baby is a mobile health education program that 
provides free, brief, evidence-based, health messages to women who are 
pregnant or have an infant under one year of age. An educational 
program led by the National Healthy Mothers, Healthy Babies coalition 
(HMHB), Text4baby is intended to help women have safe and healthy 
pregnancies by empowering them with information they need to give their 
babies the best possible start in life. The Text4baby program was 
launched nationally in February 2010. Text4baby is made possible 
through a broad, public-private partnership that includes government 
and Tribal agencies, corporations, academic institutions, professional 
associations, and non-profit organizations.
    The goal of this program evaluation is to examine the 
characteristics of women who utilize the Text4baby mobile phone-based 
program, to assess their experience with the program, and to determine 
whether enrollment in Text4baby is associated with healthy behaviors 
and timely access to health care during pregnancy and an infant's first 
year of life.
    This information will help the Department of Health and Human 
Services understand the usefulness of mobile health technology and the 
potential for expanding and/or adapting mobile phone messaging to 
additional health topics or conditions. The study also may offer 
insight into planning and implementing similar projects.
    Purpose: The purpose of the evaluation is to assess the usefulness 
of the Text4baby program.
    The four data collection components are as follows:
     Safety Consumer Net Survey with subscribers and non-
subscribers to the Text4baby program who receive prenatal care in 
community health centers in four communities. The health centers will 
recruit eligible women, obtain their signed consent to participate in 
the study, and convey their contact information to the data collection 
contractor. Data from the telephone survey will be linked to selected 
data from electronic health records (EHRs) for respondents who consent 
to the release of their EHRs. The survey will be conducted in two 
rounds: Round 1 will include pregnant women and Round 2 will include 
the same women approximately nine months later during the postpartum 
period.
     Focus Groups with current subscribers in four communities 
to obtain more in-depth qualitative data regarding the usefulness of 
the messages and the program.
     Key Informant Interviews of a diverse mix of providers in 
four communities to obtain provider perspectives on the usefulness of 
the Text4baby programs. Providers could include physicians, midwives, 
nurses, case managers, outreach workers, and health educators.
     Stakeholder Interviews with Text4baby partners (public and 
private) to examine the implementation of Text4baby at the national, 
regional, state, or local level, including outreach, enrollment, 
coalition building, sustainability, and replication.
    The annual estimate of burden is as follows:

--------------------------------------------------------------------------------------------------------------------------------------------------------
                                                                             Number of     Responses per       Total         Hours per     Total burden
                Instrument                     Person incurring burden      respondents     respondent       responses       response          hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Consent Training and Coordination.........  Health Center Study                        8              12              96            1.00              96
                                             Coordinators.
                                            Health Center Staff.........              32               1              32            1.00              32
Prenatal Patient Consent..................  Health Center Staff.........            1630               1            1630            0.08             130
                                            Prenatal Patient............            1630               1            1630            0.08             130
Parent-of-Minor Consent...................  Health Center Staff.........             195               1             195            0.25              49
                                            Parent of Minor.............             195               1             195            0.08              16
Safety Net Consumer Survey Round 1........  Prenatal Patient............             960               1             960            0.33             317
Safety Net Consumer Survey Round 2........  Postpartum Patient..........             768               1             768            0.33             253
Focus Groups..............................  Prenatal/Postpartum Patient.              80               1              80            1.50             120
Key Informant Interviews..................  Providers...................              40               1              40            0.75              30
Stakeholder Interviews....................  Stakeholders................              30               1              30            0.75              23
                                           -------------------------------------------------------------------------------------------------------------
    Total.................................  ............................  ..............  ..............  ..............  ..............            1196
--------------------------------------------------------------------------------------------------------------------------------------------------------


[[Page 63932]]

Written comments and recommendations concerning the proposed 
information collection should be sent within 30 days of this notice to 
the desk officer for HRSA, either by e-mail to OIRA_submission@omb.eop.gov or by fax to 202-395-6974. Please direct all 
correspondence to the ``attention of the desk officer for HRSA.''

    Dated: October 7, 2011.
Reva Harris,
Acting Director, Division of Policy and Information Coordination.
[FR Doc. 2011-26590 Filed 10-13-11; 8:45 am]
BILLING CODE 4165-15-P