Revision to Proposed Collection; Comment Request; Formative Research Methodology Studies for the National Children's Study, 23608-23609 [2011-10171]

Download as PDF 23608 Federal Register / Vol. 76, No. 81 / Wednesday, April 27, 2011 / Notices Health, 6011 Executive Blvd., Room 206 (MSC 7650), Bethesda, Maryland 20892–7650. Dr. Hernandez may be contacted via e-mail at mh35c@.nih.gov or by calling 301–496–0180. Comments 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. Dated: April 20, 2011. Lawrence A. Tabak, Deputy Director, National Institutes of Health. [FR Doc. 2011–10186 Filed 4–26–11; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES (2) Investigate basic mechanisms of developmental disorders and environmental factors, both risk and protective, that influence health and developmental processes. (c) REQUIREMENT.—The study under subsection (b) shall— (1) Incorporate behavioral, emotional, educational, and contextual consequences to enable a complete assessment of the physical, chemical, biological, and psychosocial environmental influences on children’s wellbeing; (2) Gather data on environmental influences and outcomes on diverse populations of children, which may include the consideration of prenatal exposures; and (3) Consider health disparities among children, which may include the consideration of prenatal exposures. Title: Formative Research and Pilot Methodology Studies for the National Children’s Study (NCS). Type of Information Collection Request: RENEWAL of OMB Clearance 0925–0590, Expiration June 30, 2011. Need and Use of Information Collection: The Children’s Health Act of 2000 (Public Law 106–310) states: To fulfill the requirements of the Children’s Health Act, the results of formative research and pilot tests will be used to maximize the efficiency of NCS procedures, materials, and methods for outreach, engagement of stakeholders, recruitment and retention of Study subjects, and to ensure scientifically robust data collection methodologies for the National Children’s Study (NCS) Vanguard and Main Studies. With this submission, the NCS seeks to renew its OMB generic clearance to conduct survey and instrument design and administration, focus groups, cognitive interviews, and health and social service provider feedback information collection surrounding outreach, engagement, recruitment, consent and questionnaire design, and retention activities. Under separate notice, the NCS also requests OMB generic clearance for formative research featuring environmental, neurodevelopmental, and study logistic information collection. These separate and distinct generic clearances will facilitate the efficiency of submission and review of these projects as required by the OMB Office of Information and Regulatory Affairs. (a) PURPOSE.—It is the purpose of this section to authorize the National Institute of Child Health and Human Development* to conduct a national longitudinal study of environmental influences (including physical, chemical, biological, and psychosocial) on children’s health and development. (b) IN GENERAL.—The Director of the National Institute of Child Health and Human Development* shall establish a consortium of representatives from appropriate Federal agencies (including the Centers for Disease Control and Prevention, the Environmental Protection Agency) to— (1) Plan, develop, and implement a prospective cohort study, from birth to adulthood, to evaluate the effects of both chronic and intermittent exposures on child health and human development; and Background The National Children’s Study is a prospective, national longitudinal study of the interaction between environment, genetics on child health and development. The Study defines ‘‘environment’’ broadly, taking a number of natural and man-made environmental, biological, genetic, and psychosocial factors into account. By studying children through their different phases of growth and development, researchers will be better able to understand the role these factors have on health and disease. Findings from the Study will be made available as the research progresses, making potential benefits known to the public National Institutes of Health Revision to Proposed Collection; Comment Request; Formative Research Methodology Studies for the National Children’s Study In compliance with the requirement of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, for opportunity for public comment on proposed data collection projects, the National Institute of Child Health and Human Development (NICHD), the National Institutes of Health (NIH) will publish periodic summaries of proposed projects to be submitted to the Office of Management and Budget (OMB) for review and approval. SUMMARY: WReier-Aviles on DSKGBLS3C1PROD with NOTICES Proposed Collection VerDate Mar<15>2010 15:36 Apr 26, 2011 Jkt 223001 PO 00000 Frm 00073 Fmt 4703 Sfmt 4703 as soon as possible. The National Children’s Study is led by a consortium of Federal partners: The U.S. Department of Health and Human Services (including the Eunice Kennedy Shriver National Institute of Child Health and Human Development and the National Institute of Environmental Health Sciences of the National Institutes of Health and the Centers for Disease Control and Prevention), and the U.S. Environmental Protection Agency. To conduct the detailed preparation needed for a study of this size and complexity, the NCS was designed to include a preliminary pilot study known as the Vanguard Study. The purpose of the Vanguard Study is to assess the feasibility, acceptability, and cost of the recruitment strategy, study procedures, and outcome assessments that are to be used in the NCS Main Study. The Vanguard Study begins prior to the NCS Main Study and will run in parallel with the Main Study. At every phase of the NCS, the multiple methodological studies conducted during the Vanguard phase will inform the implementation and analysis plan for the Main Study. The results from formative research and pilot tests proposed will inform the feasibility (scientific robustness), acceptability (burden to participants and study logistics) and cost of NCS Vanguard and Main Study recruitment, retention, study visit measures and study logistics in a manner that minimizes public information collection burden compared to burden anticipated if these projects were incorporated directly into either the NCS Vanguard or Main Study. With this submission, the NCS seeks to renew its OMB generic clearance to conduct survey and instrument design and administration, focus groups, cognitive interviews, and health and social service provider feedback information collection surrounding outreach, engagement, recruitment, consent and questionnaire design, and retention activities. Under separate notice, the NCS also requests OMB generic clearance for formative research featuring environmental, neurodevelopmental, and study logistic information collection. These separate and distinct generic clearances will facilitate the efficiency of submission and review of these projects as required by the OMB Office of Information and Regulatory Affairs. Frequency of Response: Annual [As needed on an on-going and concurrent basis]. E:\FR\FM\27APN1.SGM 27APN1 23609 Federal Register / Vol. 76, No. 81 / Wednesday, April 27, 2011 / Notices Affected Public: Members of the public, researchers, practitioners, and other health professionals. Type of Respondents: Women of child-bearing age, fathers, community leaders, members, and organizations, health care facilities and professionals, public health, environmental, social and cognitive science professional organizations and practitioners, hospital administrators, cultural and faith-based centers, and schools and child care organizations. These include both persons enrolled in the NCS Vanguard Study and their peers who are not participating in the NCS Vanguard Study. Annual reporting burden: See Table 1. The annualized cost to respondents is estimated at: $300,000 (based on $10 per hour). There are no Capital Costs to report. There are no Operating or Maintenance Costs to report. TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN SUMMARY Estimated number of responses per respondent Estimated number of respondents Average burden hours per response Estimated total annual burden hours requested Data collection activity Type of respondent Small, focused survey and instrument design and administration. NCS participants .............................. 4,000 2 1 8,000 Members of NCS target population (not NCS participants). Health and Social Service Providers Community Stakeholders ................. NCS participants .............................. Members of NCS target population (not NCS participants). Health and Social Service Providers Community Stakeholders ................. NCS participants .............................. Members of NCS target population (not NCS participants). 4,000 2 1 8,000 2,000 2,000 2,000 2,000 1 1 1 1 1 1 2 2 2,000 2,000 2,000 2,000 2,000 2,000 500 500 1 1 1 1 2 2 2 2 2,000 2,000 1,000 1,000 ........................................................... 21,000 ........................ ........................ 30,000 hrs Focus groups .................................... Cognitive interviews .......................... Total ........................................... Request for Comments: Written comments and/or suggestions from the public and affected agencies are invited on one or more of the following points: (1) Whether the proposed collection of information is necessary for the proper performance of the function of the agency, including whether the information will have practical utility; (2) The accuracy of the agency’s estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (3) Ways to minimize the burden of the collection of information on those who are to respond, including the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology. To request more information on the proposed project or to obtain a copy of the data collection plans and instruments, contact Dr. Sarah L. Glavin, Deputy Director, Office of Science Policy, Analysis and Communication, National Institute of Child Health and Human Development, 31 Center Drive Room 2A18, Bethesda, Maryland 20892, or call non-toll free number (301) 496–1877 or E-mail your request, including your address to glavins@mail.nih.gov. WReier-Aviles on DSKGBLS3C1PROD with NOTICES FOR FURTHER INFORMATION CONTACT: VerDate Mar<15>2010 15:36 Apr 26, 2011 Jkt 223001 Comments Due Date: Comments regarding this information collection are best assured of having their full effect if received within 60 days of the date of this publication. Dated: April 20, 2011. Sarah L. Glavin, Deputy Director, Office of Science Policy, Analysis and Communications, National Institute of Child Health and Human Development. [FR Doc. 2011–10171 Filed 4–26–11; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health New Proposed Collection; Comment Request; Biospecimen and Physical Measures Formative Research Methodology Studies for the National Children’s Study In compliance with the requirement of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, for opportunity for public comment on proposed data collection projects, the National Institute of Child Health and Human Development (NICHD), the National Institutes of Health (NIH) will publish periodic summaries of proposed projects to be submitted to the Office of SUMMARY: PO 00000 Frm 00074 Fmt 4703 Sfmt 4703 Management and Budget (OMB) for review and approval. Proposed Collection: Title: Biospecimen and Physical Measures Formative Research Methodology Studies for the National Children’s Study (NCS) Type of Information Collection Request: Generic Clearance Need and Use of Information Collection: The Children’s Health Act of 2000 (Pub. L. 106–310) states: (a) PURPOSE.—It is the purpose of this section to authorize the National Institute of Child Health and Human Development* to conduct a national longitudinal study of environmental influences (including physical, chemical, biological, and psychosocial) on children’s health and development. (b) IN GENERAL.—The Director of the National Institute of Child Health and Human Development * shall establish a consortium of representatives from appropriate Federal agencies (including the Centers for Disease Control and Prevention, the Environmental Protection Agency) to— (1) Plan, develop, and implement a prospective cohort study, from birth to adulthood, to evaluate the effects of both chronic and intermittent exposures on child health and human development; and (2) Investigate basic mechanisms of developmental disorders and environmental factors, both risk and protective, that influence health and developmental processes. (c) REQUIREMENT.—The study under subsection (b) shall— E:\FR\FM\27APN1.SGM 27APN1

Agencies

[Federal Register Volume 76, Number 81 (Wednesday, April 27, 2011)]
[Notices]
[Pages 23608-23609]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-10171]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Revision to Proposed Collection; Comment Request; Formative 
Research Methodology Studies for the National Children's Study

SUMMARY: In compliance with the requirement of Section 3506(c)(2)(A) of 
the Paperwork Reduction Act of 1995, for opportunity for public comment 
on proposed data collection projects, the National Institute of Child 
Health and Human Development (NICHD), the National Institutes of Health 
(NIH) will publish periodic summaries of proposed projects to be 
submitted to the Office of Management and Budget (OMB) for review and 
approval.

Proposed Collection

    Title: Formative Research and Pilot Methodology Studies for the 
National Children's Study (NCS).
    Type of Information Collection Request: RENEWAL of OMB Clearance 
0925-0590, Expiration June 30, 2011.
    Need and Use of Information Collection: The Children's Health Act 
of 2000 (Public Law 106-310) states:

    (a) PURPOSE.--It is the purpose of this section to authorize the 
National Institute of Child Health and Human Development* to conduct 
a national longitudinal study of environmental influences (including 
physical, chemical, biological, and psychosocial) on children's 
health and development.
    (b) IN GENERAL.--The Director of the National Institute of Child 
Health and Human Development* shall establish a consortium of 
representatives from appropriate Federal agencies (including the 
Centers for Disease Control and Prevention, the Environmental 
Protection Agency) to--
    (1) Plan, develop, and implement a prospective cohort study, 
from birth to adulthood, to evaluate the effects of both chronic and 
intermittent exposures on child health and human development; and
    (2) Investigate basic mechanisms of developmental disorders and 
environmental factors, both risk and protective, that influence 
health and developmental processes.
    (c) REQUIREMENT.--The study under subsection (b) shall--
    (1) Incorporate behavioral, emotional, educational, and 
contextual consequences to enable a complete assessment of the 
physical, chemical, biological, and psychosocial environmental 
influences on children's well-being;
    (2) Gather data on environmental influences and outcomes on 
diverse populations of children, which may include the consideration 
of prenatal exposures; and
    (3) Consider health disparities among children, which may 
include the consideration of prenatal exposures.

    To fulfill the requirements of the Children's Health Act, the 
results of formative research and pilot tests will be used to maximize 
the efficiency of NCS procedures, materials, and methods for outreach, 
engagement of stakeholders, recruitment and retention of Study 
subjects, and to ensure scientifically robust data collection 
methodologies for the National Children's Study (NCS) Vanguard and Main 
Studies. With this submission, the NCS seeks to renew its OMB generic 
clearance to conduct survey and instrument design and administration, 
focus groups, cognitive interviews, and health and social service 
provider feedback information collection surrounding outreach, 
engagement, recruitment, consent and questionnaire design, and 
retention activities. Under separate notice, the NCS also requests OMB 
generic clearance for formative research featuring environmental, 
neurodevelopmental, and study logistic information collection. These 
separate and distinct generic clearances will facilitate the efficiency 
of submission and review of these projects as required by the OMB 
Office of Information and Regulatory Affairs.

Background

    The National Children's Study is a prospective, national 
longitudinal study of the interaction between environment, genetics on 
child health and development. The Study defines ``environment'' 
broadly, taking a number of natural and man-made environmental, 
biological, genetic, and psychosocial factors into account. By studying 
children through their different phases of growth and development, 
researchers will be better able to understand the role these factors 
have on health and disease. Findings from the Study will be made 
available as the research progresses, making potential benefits known 
to the public as soon as possible. The National Children's Study is led 
by a consortium of Federal partners: The U.S. Department of Health and 
Human Services (including the Eunice Kennedy Shriver National Institute 
of Child Health and Human Development and the National Institute of 
Environmental Health Sciences of the National Institutes of Health and 
the Centers for Disease Control and Prevention), and the U.S. 
Environmental Protection Agency.
    To conduct the detailed preparation needed for a study of this size 
and complexity, the NCS was designed to include a preliminary pilot 
study known as the Vanguard Study. The purpose of the Vanguard Study is 
to assess the feasibility, acceptability, and cost of the recruitment 
strategy, study procedures, and outcome assessments that are to be used 
in the NCS Main Study. The Vanguard Study begins prior to the NCS Main 
Study and will run in parallel with the Main Study. At every phase of 
the NCS, the multiple methodological studies conducted during the 
Vanguard phase will inform the implementation and analysis plan for the 
Main Study.
    The results from formative research and pilot tests proposed will 
inform the feasibility (scientific robustness), acceptability (burden 
to participants and study logistics) and cost of NCS Vanguard and Main 
Study recruitment, retention, study visit measures and study logistics 
in a manner that minimizes public information collection burden 
compared to burden anticipated if these projects were incorporated 
directly into either the NCS Vanguard or Main Study.
    With this submission, the NCS seeks to renew its OMB generic 
clearance to conduct survey and instrument design and administration, 
focus groups, cognitive interviews, and health and social service 
provider feedback information collection surrounding outreach, 
engagement, recruitment, consent and questionnaire design, and 
retention activities. Under separate notice, the NCS also requests OMB 
generic clearance for formative research featuring environmental, 
neurodevelopmental, and study logistic information collection. These 
separate and distinct generic clearances will facilitate the efficiency 
of submission and review of these projects as required by the OMB 
Office of Information and Regulatory Affairs.
    Frequency of Response: Annual [As needed on an on-going and 
concurrent basis].

[[Page 23609]]

    Affected Public: Members of the public, researchers, practitioners, 
and other health professionals.
    Type of Respondents: Women of child-bearing age, fathers, community 
leaders, members, and organizations, health care facilities and 
professionals, public health, environmental, social and cognitive 
science professional organizations and practitioners, hospital 
administrators, cultural and faith-based centers, and schools and child 
care organizations. These include both persons enrolled in the NCS 
Vanguard Study and their peers who are not participating in the NCS 
Vanguard Study.
    Annual reporting burden: See Table 1. The annualized cost to 
respondents is estimated at: $300,000 (based on $10 per hour). There 
are no Capital Costs to report. There are no Operating or Maintenance 
Costs to report.

                               Table 1--Estimated Annual Reporting Burden Summary
----------------------------------------------------------------------------------------------------------------
                                                                     Estimated                       Estimated
                                     Type of         Estimated       number of        Average      total annual
   Data collection activity        respondent        number of    responses  per   burden hours    burden hours
                                                    respondents      respondent    per response      requested
----------------------------------------------------------------------------------------------------------------
Small, focused survey and       NCS participants           4,000               2               1           8,000
 instrument design and
 administration.
                                Members of NCS             4,000               2               1           8,000
                                 target
                                 population (not
                                 NCS
                                 participants).
                                Health and                 2,000               1               1           2,000
                                 Social Service
                                 Providers.
                                Community                  2,000               1               1           2,000
                                 Stakeholders.
Focus groups..................  NCS participants           2,000               1               2           2,000
                                Members of NCS             2,000               1               2           2,000
                                 target
                                 population (not
                                 NCS
                                 participants).
                                Health and                 2,000               1               2           2,000
                                 Social Service
                                 Providers.
                                Community                  2,000               1               2           2,000
                                 Stakeholders.
Cognitive interviews..........  NCS participants             500               1               2           1,000
                                Members of NCS               500               1               2           1,000
                                 target
                                 population (not
                                 NCS
                                 participants).
                                                 ---------------------------------------------------------------
    Total.....................  ................          21,000  ..............  ..............      30,000 hrs
----------------------------------------------------------------------------------------------------------------

    Request for Comments: Written comments and/or suggestions from the 
public and affected agencies are invited on one or more of the 
following points: (1) Whether the proposed collection of information is 
necessary for the proper performance of the function of the agency, 
including whether the information will have practical utility; (2) The 
accuracy of the agency's estimate of the burden of the proposed 
collection of information, including the validity of the methodology 
and assumptions used; (3) Ways to minimize the burden of the collection 
of information on those who are to respond, including the use of 
appropriate automated, electronic, mechanical, or other technological 
collection techniques or other forms of information technology.

FOR FURTHER INFORMATION CONTACT: To request more information on the 
proposed project or to obtain a copy of the data collection plans and 
instruments, contact Dr. Sarah L. Glavin, Deputy Director, Office of 
Science Policy, Analysis and Communication, National Institute of Child 
Health and Human Development, 31 Center Drive Room 2A18, Bethesda, 
Maryland 20892, or call non-toll free number (301) 496-1877 or E-mail 
your request, including your address to glavins@mail.nih.gov.
    Comments Due Date: Comments regarding this information collection 
are best assured of having their full effect if received within 60 days 
of the date of this publication.

    Dated: April 20, 2011.
Sarah L. Glavin,
Deputy Director, Office of Science Policy, Analysis and Communications, 
National Institute of Child Health and Human Development.
[FR Doc. 2011-10171 Filed 4-26-11; 8:45 am]
BILLING CODE 4140-01-P
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