Submission for OMB Review; Comment Request, 35257 [05-11969]

Download as PDF 35257 Federal Register / Vol. 70, No. 116 / Friday, June 17, 2005 / Notices relating health care choices with individual beliefs may help guide these educational efforts. The intent of this survey is to understand the role personal responsibility plays when people with Medicare make health care decisions; Affected Public: Individuals or Households; Number of Respondents: 1580; Total Annual Responses: 1580; Total Annual Hours: 300. To obtain copies of the supporting statement and any related forms for the proposed paperwork collections referenced above, access CMS’ Web site address at https://www.cms.hhs.gov/ regulations/pra/, or e-mail your request, including your address, phone number, OMB number, and CMS document identifier, to Paperwork@cms.hhs.gov, or call the Reports Clearance Office on (410) 786–1326. Written comments and recommendations for the proposed information collections must be mailed within 60 days of this notice to the address below: CMS, Office of Strategic Operations and Regulatory Affairs, Division of Regulations Development, Attention: Melissa Musotto, PRA Analyst, Room C4–26–05, 7500 Security Boulevard, Baltimore, Maryland 21244– 1850. Dated: June 10, 2005. Jimmy Wickliffe, Reports Clearance Officer, Office of Strategic Operations and Regulatory Affairs. [FR Doc. 05–11931 Filed 6–16–05; 8:45 am] BILLING CODE 4120–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Comment Request Title: Follow-up to the National Survey of Child and Adolescent WellBeing. OMB No.: 0970–0202. Description: The Department of Health and Human Services intends to collect data on a subset of children and families who have participated in the National Survey of Child and Adolescent Well-Being (NSCAW). The NSCAW was authorized under Section 429 of the Personal Responsibility and Work Opportunity Reconciliation Act of 1996. The survey began in November 1999 with a national sample of 5,501 children ages 0–14 who had been the subject of investigation by Child Protective Services (CPS) during the baseline data collection period, which extended from November 1999 through April 2000. Direct assessments and interviews were conducted with the children themselves, their primary caregivers, their caseworkers, and, for school-aged children, their teachers. Follow-up data collections were conducted 12 months, 18 months and 36 months post-baseline. The current data collection plan involves only a subset of 1,497 children from the original sample, that is, children who were ages 0–12 months during the baseline period. The original sample design for NSCAW was stratified to include an over-sample of infants; thus, the subset that is the subject of this data collection is a representative sample of infants who were the targets of CPS investigations during the survey’s baseline data collection period. This group will be at the beginning of their formal schooling as the next data collection begins, and will allow for the identification of early risk and protective factors, as well as the influence of services and service systems, on their functioning as they enter this critical transition period. The NSCAW is unique in that it is the only source of nationally representative, firsthand information about the functioning and well-being, service needs and service utilization of children and families who come to the attention of the child welfare system. Information is collected about children’s cognitive, social, emotional, behavioral and adaptive functioning, as well as family and community factors that are likely to influence their functioning. Family service needs and service utilization also are addressed in the data collection. The data collection for the follow-up will follow the same format as that used in previous rounds of data collection, and will employ the same instruments that have been used with 5- to 7-yearolds in previous rounds. Data from NSCAW are made available to the research community through licensing arrangements from the National Data Archive on Child Abuse and Neglect, housed at Cornell University. Respondents: Children, who are clients of the child welfare system, their primary caregivers, caseworkers, and teachers. ANNUAL BURDEN ESTIMATES Number of respondents Instrument Number of responses per respondent Average burden hours per response 1,017 1,017 299 790 299 1 1 1 1 1 1.10 1.40 .75 .75 1.25 Child Interview ................................................................................................. Caregiver Interview .......................................................................................... Caseworker Interview ...................................................................................... Teacher Questionnaire .................................................................................... Salivary cortisol collection ................................................................................ Estimated Total Annual Burden Hours: 3,733. Additional Information: Copies of the proposed collection may be obtained by writing to the Administration for Children and Families, Office of Administration, Office of Information Services, 370 L’Enfant Promnade, SW., Washington, DC 20447, Attn: ACF Reports Clearance Officer. All requests should be identified by the title of the VerDate jul<14>2003 17:59 Jun 16, 2005 Jkt 205001 information collection. E-mail address: grjohnson@acf.hhs.gov. OMB Comment: OMB is required to make a decision concerning the collection of information between 30 and 60 days after publication of this document in the Federal Register. Therefore, a comment is best assured of having its full effect if OMB receives it within 30 days of publication. Written comments and recommendations for the proposed information collection should PO 00000 Frm 00037 Fmt 4703 Sfmt 4703 Total burden hours 1,119 1,424 224 592 374 be sent directly to the following: Office of Management and Budget, Paperwork Reduction Project, Attn: Desk Officer for ACF, E-mail address: Katherine_T._ Astrich@omb.eo.gov. Dated: June 13, 2005. Robert Sargis, Reports Clearance Officer. [FR Doc. 05–11969 Filed 6–16–05; 8:45 am] BILLING CODE 4184–01–M E:\FR\FM\17JNN1.SGM 17JNN1

Agencies

[Federal Register Volume 70, Number 116 (Friday, June 17, 2005)]
[Notices]
[Page 35257]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-11969]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Submission for OMB Review; Comment Request

    Title: Follow-up to the National Survey of Child and Adolescent 
Well-Being.
    OMB No.: 0970-0202.
    Description: The Department of Health and Human Services intends to 
collect data on a subset of children and families who have participated 
in the National Survey of Child and Adolescent Well-Being (NSCAW). The 
NSCAW was authorized under Section 429 of the Personal Responsibility 
and Work Opportunity Reconciliation Act of 1996. The survey began in 
November 1999 with a national sample of 5,501 children ages 0-14 who 
had been the subject of investigation by Child Protective Services 
(CPS) during the baseline data collection period, which extended from 
November 1999 through April 2000. Direct assessments and interviews 
were conducted with the children themselves, their primary caregivers, 
their caseworkers, and, for school-aged children, their teachers.
    Follow-up data collections were conducted 12 months, 18 months and 
36 months post-baseline. The current data collection plan involves only 
a subset of 1,497 children from the original sample, that is, children 
who were ages 0-12 months during the baseline period. The original 
sample design for NSCAW was stratified to include an over-sample of 
infants; thus, the subset that is the subject of this data collection 
is a representative sample of infants who were the targets of CPS 
investigations during the survey's baseline data collection period. 
This group will be at the beginning of their formal schooling as the 
next data collection begins, and will allow for the identification of 
early risk and protective factors, as well as the influence of services 
and service systems, on their functioning as they enter this critical 
transition period.
    The NSCAW is unique in that it is the only source of nationally 
representative, firsthand information about the functioning and well-
being, service needs and service utilization of children and families 
who come to the attention of the child welfare system. Information is 
collected about children's cognitive, social, emotional, behavioral and 
adaptive functioning, as well as family and community factors that are 
likely to influence their functioning. Family service needs and service 
utilization also are addressed in the data collection. The data 
collection for the follow-up will follow the same format as that used 
in previous rounds of data collection, and will employ the same 
instruments that have been used with 5- to 7-year-olds in previous 
rounds. Data from NSCAW are made available to the research community 
through licensing arrangements from the National Data Archive on Child 
Abuse and Neglect, housed at Cornell University.
    Respondents: Children, who are clients of the child welfare system, 
their primary caregivers, caseworkers, and teachers.

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
                   Instrument                        Number of     responses per     hours per     Total burden
                                                    respondents     respondent       response          hours
----------------------------------------------------------------------------------------------------------------
Child Interview.................................           1,017               1            1.10           1,119
Caregiver Interview.............................           1,017               1            1.40           1,424
Caseworker Interview............................             299               1             .75             224
Teacher Questionnaire...........................             790               1             .75             592
Salivary cortisol collection....................             299               1            1.25             374
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 3,733.
    Additional Information: Copies of the proposed collection may be 
obtained by writing to the Administration for Children and Families, 
Office of Administration, Office of Information Services, 370 L'Enfant 
Promnade, SW., Washington, DC 20447, Attn: ACF Reports Clearance 
Officer. All requests should be identified by the title of the 
information collection. E-mail address: grjohnson@acf.hhs.gov.
    OMB Comment: OMB is required to make a decision concerning the 
collection of information between 30 and 60 days after publication of 
this document in the Federal Register. Therefore, a comment is best 
assured of having its full effect if OMB receives it within 30 days of 
publication. Written comments and recommendations for the proposed 
information collection should be sent directly to the following: Office 
of Management and Budget, Paperwork Reduction Project, Attn: Desk 
Officer for ACF, E-mail address: Katherine--T.-- Astrich@omb.eo.gov.

    Dated: June 13, 2005.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 05-11969 Filed 6-16-05; 8:45 am]
BILLING CODE 4184-01-M
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