Agency Information Collection Activities: Submission for OMB Review; Comment Request, 61108-61110 [2011-25374]

Download as PDF 61108 Federal Register / Vol. 76, No. 191 / Monday, October 3, 2011 / Notices anonymity. Counselors will be asked to complete the form for 100% of imminent risk callers to the eight centers participating in the evaluation. This form requests information in 14 content areas, each with multiple subitems and response options. Response options include open-ended, yes/no, Likert-type ratings, and multiple choice/ check all that apply. The form also requests demographic information on the caller, the identification of the center and counselor submitting the form, and the date of the call. Specifically, the form is divided into the following sections: (1) Call type, (2) gender, (3) age, (4) suicidal desire, (5) suicidal intent, (6) suicidal capability, (7) buffers to suicide, (8) interventions agreed to by caller or implemented by counselor without consent, (9) whether imminent risk was reduced enough such that active rescue was not needed, (10) interventions for third party callers calling about a person at imminent risk, (11) if supervisory consultation occurred, (12) barriers to getting needed help to the person at imminent risk, (13) steps taken to confirm emergency contact was made with person at risk, and (14) steps taken when emergency contact was NOT made with person at risk. The form will take approximately 15 minutes to complete and may be completed by the counselor during or after the call. It is expected that a total of 1,440 forms will be completed by 360 counselors over the two-year data collection period. The estimated response burden to collect this information is annualized over the requested two-year clearance period and is presented below: TOTAL AND ANNUALIZED AVERAGES: RESPONDENTS, RESPONSES AND HOURS Instrument Number of respondents Responses/ respondent Total responses Hours per response Total hour burden National Suicide Prevention Lifeline—Imminent Risk Form 360 2 720 .25 180 Written comments and recommendations concerning the proposed information collection should be sent by November 2, 2011 to the SAMHSA Desk Officer at the Office of Information and Regulatory Affairs, Office of Management and Budget (OMB). To ensure timely receipt of comments, and to avoid potential delays in OMB’s receipt and processing of mail sent through the U.S. Postal Service, commenters are encouraged to submit their comments to OMB via e-mail to: OIRA_Submission@omb.eop.gov. Although commenters are encouraged to send their comments via e-mail, commenters may also fax their comments to: 202–395–7285. Commenters may also mail them to: Office of Management and Budget, Office of Information and Regulatory Affairs, New Executive Office Building, Room 10102, Washington, DC 20503. Rose Shannon, Director, Division of Executive Correspondence. [FR Doc. 2011–25375 Filed 9–30–11; 8:45 am] BILLING CODE 4162–20–P DEPARTMENT OF HEALTH AND HUMAN SERVICES srobinson on DSK4SPTVN1PROD with NOTICES Substance Abuse and Mental Health Services Administration Agency Information Collection Activities: Submission for OMB Review; Comment Request Periodically, the Substance Abuse and Mental Health Services Administration (SAMHSA) will publish a summary of information collection requests under OMB review, in compliance with the VerDate Mar<15>2010 16:42 Sep 30, 2011 Jkt 223001 Paperwork Reduction Act (44 U.S.C. Chapter 35). To request a copy of these documents, call the SAMHSA Reports Clearance Officer on (240) 276–1243. Project: Cross-Site Evaluation of the Minority Substance Abuse/HIV Prevention Program—(OMB No. 0930– 0298)—Revision The Substance Abuse and Mental Health Services Administration (SAMHSA), Center for Substance Abuse Prevention (CSAP) is requesting from the Office of Management and Budget (OMB) approval for the revision of data collection activities for the cross-site study of the Minority HIV/AIDS Initiative (MAI), which includes both youth and adult questionnaires. This revision includes the addition of 4 cohorts, changes to the data collection procedures based on intervention duration, and the addition of two questions on binge drinking behavior. The current approval is under OMB No. 0930–0298, which expires on 4/30/12. This cross-site evaluation supports two of SAMHSA’s 8 Strategic Initiatives: Prevention of Substance Abuse and Mental Illness and Data, Outcomes, and Quality. It builds on six previous grant programs funded by SAMHSA’s CSAP to provide substance abuse and HIV prevention services for minority populations. The first two were planning grant programs and the last four were service grant programs. The goals for the Cohort 3–6 grants were to add, increase, or enhance integrated substance abuse (SA) and HIV prevention services by providing supportive services and strengthening linkages between service providers for at-risk minority populations. The HIV Cohort 1–3 previously received PO 00000 Frm 00037 Fmt 4703 Sfmt 4703 clearance under OMB No. 0930–0208 and Cohort 6 grants previously received clearance under OMB No. 0930–0298. Since neither the HIV Cohort 4 nor the Cohort 5 Programs were cross-site studies, they did not require OMB clearance. The current HIV Minority SA/HIV Prevention Program funded: • Cohorts 7 and 8 Prevention of Substance Abuse (SA) and HIV for AtRisk Racial/Ethnic Minority Subpopulations Cooperative Agreements—60 grants for 5 years, • Cohort 9 Ready-To-Respond Initiative—35 grants for 5 years and, • Cohort 10 Capacity Building Initiative—27 grants for 5 years. Grantees are community based organizations that are required to address the SAMHSA Strategic Prevention Framework (SPF) and participate in this cross-site evaluation. The grantees are expected to provide leadership and coordination on the planning and implementation of the SPF that targets minority populations, the minority reentry population, as well as other high risk groups residing in communities of color with high prevalence of SA and HIV/AIDS. The primary objectives of the cross-site study are to: (1) Determine the success of the MAI in preventing, delaying, and/ or reducing the use of alcohol, tobacco, and other drugs (ATOD) among the target populations. The results of this cross-site study will assist SAMHSA/ CSAP in promoting and disseminating optimally effective prevention programs; (2) Measure the effectiveness of evidence-based programs and infrastructure development activities such as: outreach and training, mobilization of key stakeholders, substance abuse and HIV/AIDS E:\FR\FM\03OCN1.SGM 03OCN1 61109 Federal Register / Vol. 76, No. 191 / Monday, October 3, 2011 / Notices counseling and education, referrals to appropriate medical treatment and/or other intervention strategies (i.e., cultural enrichment activities, educational and vocational resources, and computer-based curricula); and (3) Assess the process of adopting and implementing the Strategic Prevention Framework (SPF) with the target populations. The grantees are expected to provide an effective prevention process, direction, and a common set of goals, expectations, and accountabilities to be adapted and integrated at the community level. While the grantees have substantial flexibility in choosing their individual evidence-based programs, they are all required to base them on the five steps of the SPF to build service capacity specific to SA and HIV prevention services. Conducting this cross-site evaluation will assist SAMHSA/CSAP in promoting and disseminating optimally effective prevention programs. Grantees must also conduct ongoing monitoring and evaluation of their projects to assess program effectiveness including Federal reporting of the Government Performance and Results Act (GPRA) of 1993, SAMHSA/CSAP National Outcome Measures (NOMs), and HIV Counseling and Testing. All of this information will be collected through self-report questionnaires administered to program participants. All grantees will use two instruments, one for youth aged between 12 and 17 and one for adults aged 18 and older. Participants in interventions lasting 30 days or longer will complete questionnaires three times, taking an average of 50 minutes for baseline, exit, and follow-up questionnaires. Participants in interventions lasting 2– 29 days will complete questionnaires two times taking an average of 30 minutes to complete. Single-session intervention participants will complete one questionnaire at exit only. The GPRA and NOMs measures on the instruments have already been approved by OMB (OMB No. 0930–0230), and the remaining HIV-related questions have been approved under OMB No. 0930– 0298.The youth questionnaire contains 125 questions, of which 28 relate to HIV/AIDS and the adult questionnaire contains 118 items, 47 of which relate to HIV/AIDS. Two additional questions have been added to address SAMHSA’s need to collect information on binge drinking behavior. These questions are: 1. Females only: During the past 30 days, on how many days did you have 4 or more drinks on the same occasion? 2. Males only: During the past 30 days, on how many days did you have 5 or more drinks on the same occasion? Sample size, respondent burden, and intrusiveness have been minimized to be consistent with the cross-site objectives. Procedures are employed to safeguard the privacy and confidentiality of participants. Every effort has been made to coordinate cross-site data collection with local data collection efforts in an attempt to minimize respondent burden. The cross-site evaluation results will have significant implications for the substance abuse and HIV/AIDS prevention fields, the allocation of grant funds, and other evaluation activities conducted by multiple Federal, State, and local government agencies. They will be used to develop Federal policy in support of SAMHSA/CSAP program initiatives, inform the public of lessons learned and findings, improve existing programs, and promote replication and dissemination of effective prevention strategies. Total Estimates of Annualized Hour Burden The following table shows the estimated annualized burden for data collection. TABLE 1A—ESTIMATES OF ANNUALIZED HOUR BURDEN BY INTERVENTION LENGTH Number of respondents Intervention length 30-Days or More Intervention: Base line ....................................................................... Exit ................................................................................ Follow-up ...................................................................... Subtotal ......................................................................... 2 to 29 Day Intervention: Base line ....................................................................... Exit ................................................................................ Subtotal ......................................................................... Single Day Intervention: Exit ................................................................................ Annualized Total ........................................................... Responses per respondent Total responses Hours per response Total hour burden 7,937 4,887 2,942 7,937 1 1 1 ........................ 7,937 4,887 2,942 15,766 0.83 0.83 0.83 ........................ 6,588 4,056 2442 13,086 1,416 872 1,416 1 1 ........................ 1,416 872 2,288 0.5 0.5 ........................ 708 436 1,144 2,458 11,811 1 ........................ 2,458 20,512 0.25 ........................ 614 14,844 TABLE 1B—ESTIMATES OF ANNUALIZED HOUR BURDEN BY SURVEY TYPE Questionnaire Number of respondents Total responses Total hour burden 9,682 2,128 16,899 3,612 12,234 2,610 Annualized Total .............................. srobinson on DSK4SPTVN1PROD with NOTICES Annualized Total Adult ................................... Annualized Total Youth ................................. 11,811 20,512 14,844 Written comments and recommendations concerning the proposed information collection should be sent by November 2, 2011 to the SAMHSA Desk Officer at the Office of Information and Regulatory Affairs, VerDate Mar<15>2010 16:42 Sep 30, 2011 Jkt 223001 Office of Management and Budget (OMB). To ensure timely receipt of comments, and to avoid potential delays in OMB’s receipt and processing of mail sent through the U.S. Postal Service, commenters are encouraged to submit PO 00000 Frm 00038 Fmt 4703 Sfmt 4703 their comments to OMB via e-mail to: OIRA_Submission@omb.eop.gov. Although commenters are encouraged to send their comments via e-mail, commenters may also fax their comments to: 202–395–7285. E:\FR\FM\03OCN1.SGM 03OCN1 61110 Federal Register / Vol. 76, No. 191 / Monday, October 3, 2011 / Notices Commenters may also mail them to: Office of Management and Budget, Office of Information and Regulatory Affairs, New Executive Office Building, Room 10102, Washington, DC 20503. Rose Shannon, Director, Division of Executive Correspondence. [FR Doc. 2011–25374 Filed 9–30–11; 8:45 am] BILLING CODE 4162–20–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Substance Abuse and Mental Health Services Administration Current List of Laboratories and Instrumented Initial Testing Facilities Which Meet Minimum Standards To Engage in Urine Drug Testing for Federal Agencies Substance Abuse and Mental Health Services Administration, HHS. ACTION: Notice. AGENCY: The Department of Health and Human Services (HHS) notifies Federal agencies of the Laboratories and Instrumented Initial Testing Facilities (IITF) currently certified to meet the standards of the Mandatory Guidelines for Federal Workplace Drug Testing Programs (Mandatory Guidelines). The Mandatory Guidelines were first published in the Federal Register on April 11, 1988 (53 FR 11970), and subsequently revised in the Federal Register on June 9, 1994 (59 FR 29908); September 30, 1997 (62 FR 51118); April 13, 2004 (69 FR 19644); November 25, 2008 (73 FR 71858); December 10, 2008 (73 FR 75122); and on April 30, 2010 (75 FR 22809). A notice listing all currently certified Laboratories and Instrumented Initial Testing Facilities (IITF) is published in the Federal Register during the first week of each month. If any Laboratory/ IITF’s certification is suspended or revoked, the Laboratory/IITF will be omitted from subsequent lists until such time as it is restored to full certification under the Mandatory Guidelines. If any Laboratory/IITF has withdrawn from the HHS National Laboratory Certification Program (NLCP) during the past month, it will be listed at the end and will be omitted from the monthly listing thereafter. This notice is also available on the Internet at http:// www.workplace.samhsa.gov and http:// www.drugfreeworkplace.gov. FOR FURTHER INFORMATION CONTACT: Mrs. Giselle Hersh, Division of Workplace Programs, SAMHSA/CSAP, Room srobinson on DSK4SPTVN1PROD with NOTICES SUMMARY: VerDate Mar<15>2010 16:42 Sep 30, 2011 Jkt 223001 2–1042, One Choke Cherry Road, Rockville, Maryland 20857; 240–276– 2600 (voice), 240–276–2610 (fax). SUPPLEMENTARY INFORMATION: The Mandatory Guidelines were initially developed in accordance with Executive Order 12564 and section 503 of Public Law 100–71. The ‘‘Mandatory Guidelines for Federal Workplace Drug Testing Programs,’’ as amended in the revisions listed above, requires {or set} strict standards that Laboratories and Instrumented Initial Testing Facilities (IITF) must meet in order to conduct drug and specimen validity tests on urine specimens for Federal agencies. To become certified, an applicant Laboratory/IITF must undergo three rounds of performance testing plus an on-site inspection. To maintain that certification, a Laboratory/IITF must participate in a quarterly performance testing program plus undergo periodic, on-site inspections. Laboratories and Instrumented Initial Testing Facilities (IITF) in the applicant stage of certification are not to be considered as meeting the minimum requirements described in the HHS Mandatory Guidelines. A Laboratory/ IITF must have its letter of certification from HHS/SAMHSA (formerly: HHS/ NIDA) which attests that it has met minimum standards. In accordance with the Mandatory Guidelines dated November 25, 2008 (73 FR 71858), the following Laboratories and Instrumented Initial Testing Facilities (IITF) meet the minimum standards to conduct drug and specimen validity tests on urine specimens: Instrumented Initial Testing Facilities (IITF) None. Laboratories ACL Laboratories, 8901 W. Lincoln Ave., West Allis, WI 53227, 414–328– 7840/800–877–7016. (Formerly: Bayshore Clinical Laboratory). ACM Medical Laboratory, Inc., 160 Elmgrove Park, Rochester, NY 14624, 585–429–2264. Advanced Toxicology Network, 3560 Air Center Cove, Suite 101, Memphis, TN 38118, 901–794–5770/888–290– 1150. Aegis Analytical Laboratories, 345 Hill Ave., Nashville, TN 37210, 615–255– 2400. (Formerly: Aegis Sciences Corporation, Aegis Analytical Laboratories, Inc.) Alere Toxicology Services, 1111 Newton St., Gretna, LA 70053, 504–361–8989/ 800–433 –3823. (Formerly: Kroll Laboratory Specialists, Inc., Laboratory Specialists, Inc.) PO 00000 Frm 00039 Fmt 4703 Sfmt 4703 Alere Toxicology Services, 450 Southlake Blvd., Richmond, VA 23236, 804–378–9130. (Formerly: Kroll Laboratory Specialists, Inc., Scientific Testing Laboratories, Inc.; Kroll Scientific Testing Laboratories, Inc.) Baptist Medical Center-Toxicology Laboratory, 11401 I–30, Little Rock, AR 72209–7056, 501–202–2783. (Formerly: Forensic Toxicology Laboratory Baptist Medical Center.) Clinical Reference Lab, 8433 Quivira Road, Lenexa, KS 66215–2802, 800– 445–6917. Doctors Laboratory, Inc., 2906 Julia Drive, Valdosta, GA 31602, 229–671– 2281. DrugScan, Inc., P.O. Box 2969, 1119 Mearns Road, Warminster, PA 18974, 215–674–9310. ElSohly Laboratories, Inc., 5 Industrial Park Drive, Oxford, MS 38655, 662– 236–2609. Gamma-Dynacare Medical Laboratories,* A Division of the Gamma-Dynacare Laboratory Partnership, 245 Pall Mall Street, London, ONT, Canada N6A 1P4, 519– 679–1630. Laboratory Corporation of America Holdings, 7207 N. Gessner Road, Houston, TX 77040, 713–856–8288/ 800–800–2387. Laboratory Corporation of America Holdings, 69 First Ave., Raritan, NJ 08869, 908–526–2400/800–437–4986. (Formerly: Roche Biomedical Laboratories, Inc.) Laboratory Corporation of America Holdings, 1904 Alexander Drive, Research Triangle Park, NC 27709, 919–572–6900/800–833–3984. (Formerly: LabCorp Occupational Testing Service Inc., CompuChem Laboratories, Inc.; CompuChem Laboratories, Inc., A Subsidiary of Roche Biomedical Laboratory; Roche CompuChem Laboratories, Inc., A Member of the Roche Group.) Laboratory Corporation of America Holdings, 1120 Main Street, Southaven, MS 38671, 866–827–8042/ 800–233–6339. (Formerly: LabCorp Occupational Testing Services, Inc.; MedExpress/National Laboratory Center.) LabOne, Inc. d/b/a Quest Diagnostics, 10101 Renner Blvd., Lenexa, KS 66219, 913–888–3927/800–873–8845. (Formerly: Quest Diagnostics Incorporated; LabOne, Inc.; Center for Laboratory Services, a Division of LabOne, Inc.) Maxxam Analytics,* 6740 Campobello Road, Mississauga, ON, Canada L5N 2L8, 905–817–5700. (Formerly: Maxxam Analytics Inc., NOVAMANN (Ontario), Inc.) E:\FR\FM\03OCN1.SGM 03OCN1

Agencies

[Federal Register Volume 76, Number 191 (Monday, October 3, 2011)]
[Notices]
[Pages 61108-61110]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-25374]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Substance Abuse and Mental Health Services Administration


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

    Periodically, the Substance Abuse and Mental Health Services 
Administration (SAMHSA) will publish a summary of information 
collection requests under OMB review, in compliance with the Paperwork 
Reduction Act (44 U.S.C. Chapter 35). To request a copy of these 
documents, call the SAMHSA Reports Clearance Officer on (240) 276-1243.

Project: Cross-Site Evaluation of the Minority Substance Abuse/HIV 
Prevention Program--(OMB No. 0930-0298)--Revision

    The Substance Abuse and Mental Health Services Administration 
(SAMHSA), Center for Substance Abuse Prevention (CSAP) is requesting 
from the Office of Management and Budget (OMB) approval for the 
revision of data collection activities for the cross-site study of the 
Minority HIV/AIDS Initiative (MAI), which includes both youth and adult 
questionnaires. This revision includes the addition of 4 cohorts, 
changes to the data collection procedures based on intervention 
duration, and the addition of two questions on binge drinking behavior. 
The current approval is under OMB No. 0930-0298, which expires on 4/30/
12.
    This cross-site evaluation supports two of SAMHSA's 8 Strategic 
Initiatives: Prevention of Substance Abuse and Mental Illness and Data, 
Outcomes, and Quality. It builds on six previous grant programs funded 
by SAMHSA's CSAP to provide substance abuse and HIV prevention services 
for minority populations. The first two were planning grant programs 
and the last four were service grant programs. The goals for the Cohort 
3-6 grants were to add, increase, or enhance integrated substance abuse 
(SA) and HIV prevention services by providing supportive services and 
strengthening linkages between service providers for at-risk minority 
populations. The HIV Cohort 1-3 previously received clearance under OMB 
No. 0930-0208 and Cohort 6 grants previously received clearance under 
OMB No. 0930-0298. Since neither the HIV Cohort 4 nor the Cohort 5 
Programs were cross-site studies, they did not require OMB clearance. 
The current HIV Minority SA/HIV Prevention Program funded:
     Cohorts 7 and 8 Prevention of Substance Abuse (SA) and HIV 
for At-Risk Racial/Ethnic Minority Subpopulations Cooperative 
Agreements--60 grants for 5 years,
     Cohort 9 Ready-To-Respond Initiative--35 grants for 5 
years and,
     Cohort 10 Capacity Building Initiative--27 grants for 5 
years.
    Grantees are community based organizations that are required to 
address the SAMHSA Strategic Prevention Framework (SPF) and participate 
in this cross-site evaluation. The grantees are expected to provide 
leadership and coordination on the planning and implementation of the 
SPF that targets minority populations, the minority reentry population, 
as well as other high risk groups residing in communities of color with 
high prevalence of SA and HIV/AIDS. The primary objectives of the 
cross-site study are to: (1) Determine the success of the MAI in 
preventing, delaying, and/or reducing the use of alcohol, tobacco, and 
other drugs (ATOD) among the target populations. The results of this 
cross-site study will assist SAMHSA/CSAP in promoting and disseminating 
optimally effective prevention programs; (2) Measure the effectiveness 
of evidence-based programs and infrastructure development activities 
such as: outreach and training, mobilization of key stakeholders, 
substance abuse and HIV/AIDS

[[Page 61109]]

counseling and education, referrals to appropriate medical treatment 
and/or other intervention strategies (i.e., cultural enrichment 
activities, educational and vocational resources, and computer-based 
curricula); and (3) Assess the process of adopting and implementing the 
Strategic Prevention Framework (SPF) with the target populations.
    The grantees are expected to provide an effective prevention 
process, direction, and a common set of goals, expectations, and 
accountabilities to be adapted and integrated at the community level. 
While the grantees have substantial flexibility in choosing their 
individual evidence-based programs, they are all required to base them 
on the five steps of the SPF to build service capacity specific to SA 
and HIV prevention services. Conducting this cross-site evaluation will 
assist SAMHSA/CSAP in promoting and disseminating optimally effective 
prevention programs.
    Grantees must also conduct ongoing monitoring and evaluation of 
their projects to assess program effectiveness including Federal 
reporting of the Government Performance and Results Act (GPRA) of 1993, 
SAMHSA/CSAP National Outcome Measures (NOMs), and HIV Counseling and 
Testing. All of this information will be collected through self-report 
questionnaires administered to program participants. All grantees will 
use two instruments, one for youth aged between 12 and 17 and one for 
adults aged 18 and older. Participants in interventions lasting 30 days 
or longer will complete questionnaires three times, taking an average 
of 50 minutes for baseline, exit, and follow-up questionnaires. 
Participants in interventions lasting 2-29 days will complete 
questionnaires two times taking an average of 30 minutes to complete. 
Single-session intervention participants will complete one 
questionnaire at exit only. The GPRA and NOMs measures on the 
instruments have already been approved by OMB (OMB No. 0930-0230), and 
the remaining HIV-related questions have been approved under OMB No. 
0930-0298.The youth questionnaire contains 125 questions, of which 28 
relate to HIV/AIDS and the adult questionnaire contains 118 items, 47 
of which relate to HIV/AIDS. Two additional questions have been added 
to address SAMHSA's need to collect information on binge drinking 
behavior.
    These questions are:
    1. Females only: During the past 30 days, on how many days did you 
have 4 or more drinks on the same occasion?
    2. Males only: During the past 30 days, on how many days did you 
have 5 or more drinks on the same occasion?
    Sample size, respondent burden, and intrusiveness have been 
minimized to be consistent with the cross-site objectives. Procedures 
are employed to safeguard the privacy and confidentiality of 
participants. Every effort has been made to coordinate cross-site data 
collection with local data collection efforts in an attempt to minimize 
respondent burden.
    The cross-site evaluation results will have significant 
implications for the substance abuse and HIV/AIDS prevention fields, 
the allocation of grant funds, and other evaluation activities 
conducted by multiple Federal, State, and local government agencies. 
They will be used to develop Federal policy in support of SAMHSA/CSAP 
program initiatives, inform the public of lessons learned and findings, 
improve existing programs, and promote replication and dissemination of 
effective prevention strategies.

Total Estimates of Annualized Hour Burden

    The following table shows the estimated annualized burden for data 
collection.

                      Table 1a--Estimates of Annualized Hour Burden by Intervention Length
----------------------------------------------------------------------------------------------------------------
                                     Number of     Responses per       Total         Hours per      Total hour
       Intervention length          respondents     respondent       responses       response         burden
----------------------------------------------------------------------------------------------------------------
30-Days or More Intervention:
    Base line...................           7,937               1           7,937            0.83           6,588
    Exit........................           4,887               1           4,887            0.83           4,056
    Follow-up...................           2,942               1           2,942            0.83            2442
    Subtotal....................           7,937  ..............          15,766  ..............          13,086
2 to 29 Day Intervention:
    Base line...................           1,416               1           1,416             0.5             708
    Exit........................             872               1             872             0.5             436
    Subtotal....................           1,416  ..............           2,288  ..............           1,144
Single Day Intervention:
    Exit........................           2,458               1           2,458            0.25             614
    Annualized Total............          11,811  ..............          20,512  ..............          14,844
----------------------------------------------------------------------------------------------------------------


                                              Table 1b--Estimates of Annualized Hour Burden by Survey Type
--------------------------------------------------------------------------------------------------------------------------------------------------------
                         Questionnaire                              Number of respondents            Total responses              Total hour burden
--------------------------------------------------------------------------------------------------------------------------------------------------------
Annualized Total Adult........................................                         9,682                        16,899                        12,234
Annualized Total Youth........................................                         2,128                         3,612                         2,610
                                                               -----------------------------------------------------------------------------------------
        Annualized Total......................................                        11,811                        20,512                        14,844
--------------------------------------------------------------------------------------------------------------------------------------------------------

    Written comments and recommendations concerning the proposed 
information collection should be sent by November 2, 2011 to the SAMHSA 
Desk Officer at the Office of Information and Regulatory Affairs, 
Office of Management and Budget (OMB). To ensure timely receipt of 
comments, and to avoid potential delays in OMB's receipt and processing 
of mail sent through the U.S. Postal Service, commenters are encouraged 
to submit their comments to OMB via e-mail to: OIRA_Submission@omb.eop.gov. Although commenters are encouraged to send 
their comments via e-mail, commenters may also fax their comments to: 
202-395-7285.

[[Page 61110]]

Commenters may also mail them to: Office of Management and Budget, 
Office of Information and Regulatory Affairs, New Executive Office 
Building, Room 10102, Washington, DC 20503.

Rose Shannon,
Director, Division of Executive Correspondence.
[FR Doc. 2011-25374 Filed 9-30-11; 8:45 am]
BILLING CODE 4162-20-P