Agency Forms Undergoing Paperwork Reduction Act Review, 69638-69640 [2023-22271]

Download as PDF 69638 Federal Register / Vol. 88, No. 193 / Friday, October 6, 2023 / Notices The Shigella Hypothesis Generating Questionnaire (SHGQ) will be administered by state and local public health officials via telephone interviews or self-administered web-based surveys with cases of shigellosis or their proxy who are part of a shigellosis cluster or outbreak. The SHGQ will collect information on demographics characteristics, household information and family member event and activity attendance, clinical signs and symptoms, medical care and treatment information, travel history, contact with international travelers or other ill individuals, event and activity attendance, limited food and water exposure, work, visit, and volunteer locations, childcare and school attendance, and recent sexual partner(s) and activity. This interview/survey activity is consistent with the state’s existing authority to investigate reports of notifiable diseases for routine surveillance purposes; therefore, formal consent to participate in the activity is not required. However, cases may choose not to participate and may choose not to answer any question they do not wish to answer. It will take health department personnel approximately 45 minutes to administer the questionnaire to an estimated 1,500 patient respondents. This results in an estimated annual burden to the public of 1,125 hours. ESTIMATED ANNUALIZED BURDEN HOURS Type of respondents Form name Number of respondents Number of responses per respondent Average burden per response (in hours) Shigellosis case patients identified as part of outbreak or cluster investigations. Shigella Hypothesis Generating Questionnaire. 1500 1 45/60 Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Public Health Ethics and Regulations, Office of Science, Centers for Disease Control and Prevention. [FR Doc. 2023–22273 Filed 10–5–23; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30Day–24–23AQ] lotter on DSK11XQN23PROD with NOTICES1 Agency Forms Undergoing Paperwork Reduction Act Review In accordance with the Paperwork Reduction Act of 1995, the Centers for Disease Control and Prevention (CDC) has submitted the information collection request titled ‘‘Understanding HIV/STD Risk and Enhancing PrEP Implementation Messaging in a Diverse Community-Based Sample of Gay, Bisexual, and Other Men Who Have Sex with Men in a Transformational Era (MIC–DROP)’’ to the Office of Management and Budget (OMB) for review and approval. CDC previously published a ‘‘Proposed Data Collection Submitted for Public Comment and Recommendations’’ notice on November 16, 2022, to obtain comments from the public and affected agencies. CDC received two comments related to the previous notice. This notice serves to allow an additional 30 days for public and affected agency comments. CDC will accept all comments for this proposed information collection project. The Office of Management and Budget is particularly interested in comments that: VerDate Sep<11>2014 17:00 Oct 05, 2023 Jkt 262001 (a) Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; (b) Evaluate the accuracy of the agencies estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (c) Enhance the quality, utility, and clarity of the information to be collected; (d) Minimize the burden of the collection of information on those who are to respond, including, through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submission of responses; and (e) Assess information collection costs. To request additional information on the proposed project or to obtain a copy of the information collection plan and instruments, call (404) 639–7570. Comments and recommendations for the proposed information collection should be sent within 30 days of publication of this notice to www.reginfo.gov/public/ do/PRAMain. Find this particular information collection by selecting ‘‘Currently under 30-day Review—Open for Public Comments’’ or by using the search function. Direct written comments and/or suggestions regarding the items contained in this notice to the Attention: CDC Desk Officer, Office of Management and Budget, 725 17th Street NW, Washington, DC 20503 or by fax to (202) 395–5806. Provide written PO 00000 Frm 00029 Fmt 4703 Sfmt 4703 comments within 30 days of notice publication. Proposed Project ‘‘Understanding HIV/STD Risk and Enhancing PrEP Implementation Messaging in a Diverse CommunityBased Sample of Gay, Bisexual, and Other Men Who Have Sex with Men in a Transformational Era (MIC–DROP)’’— New—National Center for HIV, Viral Hepatitis, STD, TB Prevention (NCHHSTP), Centers for Disease Control and Prevention (CDC). Background and Brief Description CDC is requesting approval for three years for a data collection titled ‘‘Understanding HIV/STD Risk and Enhancing PrEP Implementation Messaging in a Diverse CommunityBased Sample of Gay, Bisexual, and Other Men Who Have Sex with Men in a Transformational Era (MIC–DROP).’’ The purpose of the information collection is to understand men’s strategies to prevent HIV and sexually transmitted infections (STIs), including preexposure prophylaxis (PrEP) use and adherence, condom use, sexual risktaking behavior, and substance-using behaviors. This study will assess men’s use and preferences for prevention modalities and their awareness, knowledge, beliefs, and perceptions about products that prevent the transmission of HIV and other sexually transmitted diseases (STD). This study will also conduct structured assessments to identify HIV prevention gaps and test prevention messages for men who have sex with men (MSM). The information collected in this study will be used to: (1) describe realworld HIV and STI prevention strategies including PrEP and condom use and E:\FR\FM\06OCN1.SGM 06OCN1 69639 Federal Register / Vol. 88, No. 193 / Friday, October 6, 2023 / Notices adherence; (2) better understand men’s use, preferences, knowledge, and perceptions about prevention modalities; (3) develop rapid reports that will allow for summary recommendations concerning gaps in prevention protection and message testing; and (4) provide timely new information to public health programs and decision makers. The study will be carried out in three cities: Atlanta, GA; Chicago, IL; and San Diego, CA. Participants will include 1,275 HIVnegative men ages 18 and older. Cohort participants will identify as cisgender male; report sex with a man in the last six months; and be fluent in written/ spoken English or Spanish. We will use purposive sampling to ensure that 60% of participants will be PrEP users at baseline, and 40% will not be using PrEP at that point. We will also oversample Black/African American and Hispanic/Latino MSM to ensure that a minimum of 30% each are represented in the cohort sample. Participants will be recruited using a combination of approaches including social media, referral, and in-person outreach. A computer-assisted quantitative assessment will collect information about participants’ use of prevention modalities, as well as their awareness, knowledge, beliefs, and perceptions about HIV/STI prevention products and prevention messages. The study will utilize the SMaRT (Study Management and Retention Toolkit) system, a study management platform for participant management that includes a HIPPAcompliant companion mobile app that study participants install on their smart phones. The app supports several key functions of study participation including notifications of surveys available, administration of surveys, a messaging center, appointment scheduling, secure HIPPA-compliant document upload and return of laboratory results, and a HIPPAcompliant telehealth video conference platform. At six-month intervals starting at baseline, all participants will be mailed self-collection kits to provide samples for HIV and STI testing. Specimens for STI testing include urine, rectal, and pharyngeal swabs for gonorrhea and chlamydia and dried blood spot (DBS) for syphilis testing. HIV kits will collect DBS for 4th generation HIV testing. Tests will be shipped from, returned to, and processed by a CLIA-certified laboratory. Participants will also have the option to self-collect their specimens at a study site, where study staff will provide them with a selfcollection kit and a private room in which to collect their specimens. A subset of the participant cohort will be invited to further participate in qualitative data collection activities including focus groups and in-depth interviews. The focus groups will assess the participants’ awareness of PrEP messages, preferences for PrEP messages, and perceived impact/efficacy of HIV prevention and PrEP messages. The in-depth interviews will assess men’s PrEP experiences, their preferences for PrEP and other HIV prevention products, and further explore their reactions to prevention messages. Participants will have the option to join virtual or in-person focus groups and interview sessions. Total study enrollment is 1,275 over the three-year data collection period. Based on screening and enrollment numbers from similar studies, we estimate we will need to screen 2,550 individuals (850 annually) to reach total enrollment. The screening process will take approximately five minutes to complete. Participants will be rescreened at the time of the enrollment visit. Contact information will be collected from 1,275 participants (425 annually) and will take approximately five minutes to complete. The quantitative assessment will take 45 minutes to complete and will be delivered to 1,275 participants (850 annually) a total 8 times. The SMaRT app install will take 10 minutes to complete and will be completed by 1,275 participants (425 annually). The specimen kit for HIV testing will take approximately 20 minutes to complete and will be distributed to 1,275 participants (850 annually) a total of four times. The specimen kit for STI testing will take approximately 30 minutes to complete and will be distributed to 1,275 participants (850 annually) a total of four times. A subset of the cohort participants will be invited to participate in qualitative data collection activities. A total of 144 participants (48 annually) will engage in a focus group that is estimated to take 90 minutes to complete, and 45 participants will be invited to participate in a series of three in-depth interviews to be administered at sixmonth intervals. The interviews will take approximately 60 minutes to complete. CDC is requesting 12,996 total burden hours across 3 years of data collection. The total estimated annualized burden hours are 4,332. Total burden for each activity has been rounded to the nearest whole hour. Participation of respondents is voluntary. There is no cost to participants other than their time. ESTIMATED ANNUALIZED BURDEN HOURS Type of respondent lotter on DSK11XQN23PROD with NOTICES1 General General General General General General General General Public—Adults Public—Adults Public—Adults Public—Adults Public—Adults Public—Adults Public—Adults Public—Adults VerDate Sep<11>2014 ................................... ................................... ................................... ................................... ................................... ................................... ................................... ................................... 17:00 Oct 05, 2023 Number of respondents Form name Jkt 262001 Eligibility Screener .......................................... Locator Form .................................................. Quarterly Assessment .................................... SMaRT App Installation ................................. Sample Collection for HIV Test ..................... Sample Collection for STI Test ...................... Focus Group .................................................. In-Depth interview .......................................... PO 00000 Frm 00030 Fmt 4703 Sfmt 4703 E:\FR\FM\06OCN1.SGM 850 425 850 425 850 850 48 45 06OCN1 Number of responses per respondent 2 1 4 1 2 2 1 1 Average burden per response (in hr) 5/60 5/60 45/60 10/60 20/60 30/60 90/60 60/60 69640 Federal Register / Vol. 88, No. 193 / Friday, October 6, 2023 / Notices Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Public Health Ethics and Regulations, Office of Science, Centers for Disease Control and Prevention. [FR Doc. 2023–22271 Filed 10–5–23; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day-24–1402; Docket No. CDC–2023– 0081] Proposed Data Collection Submitted for Public Comment and Recommendations Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). ACTION: Notice with comment period. AGENCY: The Centers for Disease Control and Prevention (CDC), as part of its continuing effort to reduce public burden and maximize the utility of government information, invites the general public and other Federal agencies the opportunity to comment on a proposed or continuing information collection, as required by the Paperwork Reduction Act of 1995. This notice invites comments on a proposed information collection titled Surveillance of HIV-related service barriers among Individuals with Early or Late HIV Diagnoses (SHIELD), which collects information from people who were recently diagnosed with HIV at early (Stage 0) or late diagnosis (Stage 3) to understand barriers to HIV prevention and testing services to contributing to transmission. DATES: CDC must receive written comments on or before December 5, 2023. SUMMARY: You may submit comments, identified by Docket No. CDC–2023– 0081 by either of the following methods: • Federal eRulemaking Portal: www.regulations.gov. Follow the instructions for submitting comments. • Mail: Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS H21–8, Atlanta, Georgia 30329. Instructions: All submissions received must include the agency name and Docket Number. CDC will post, without change, all relevant comments to www.regulations.gov. Please note: Submit all comments through the Federal eRulemaking portal lotter on DSK11XQN23PROD with NOTICES1 ADDRESSES: VerDate Sep<11>2014 17:00 Oct 05, 2023 Jkt 262001 (www.regulations.gov) or by U.S. mail to the address listed above. FOR FURTHER INFORMATION CONTACT: To request more information on the proposed project or to obtain a copy of the information collection plan and instruments, contact Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road, NE, MS H21–8, Atlanta, Georgia 30329; Telephone: 404–639–7118; Email: omb@ cdc.gov. SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501–3520), Federal agencies must obtain approval from the Office of Management and Budget (OMB) for each collection of information they conduct or sponsor. In addition, the PRA also requires Federal agencies to provide a 60-day notice in the Federal Register concerning each proposed collection of information, including each new proposed collection, each proposed extension of the existing collection of information, and each reinstatement of previously approved information collection before submitting the collection to the OMB for approval. To comply with this requirement, we are publishing this notice of a proposed data collection as described below. The OMB is particularly interested in comments that will help: 1. Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; 2. Evaluate 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. Enhance the quality, utility, and clarity of the information to be collected; 4. Minimize the burden of the collection of information on those who are to respond, including using appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submissions of responses; and 5. Assess information collection costs. Proposed Project Surveillance of HIV-related service barriers among Individuals with Early or Late HIV Diagnoses (SHIELD) (OMB Control No. 0920–1402, Exp. 5/31/ 2026)—Revision—National Center for HIV, Viral Hepatitis, STD, and TB Prevention (NCHHSTP), Centers for Disease Control and Prevention (CDC). PO 00000 Frm 00031 Fmt 4703 Sfmt 4703 Background and Brief Description National HIV Surveillance System (NHSS) data indicate that 37,968 adolescents and adults received an HIV diagnosis in the United States and dependent areas in 2018. During 2015– 2019, the overall rate of annual diagnoses decreased only slightly, from 12.4 to 11.1 per 100,000. Although not every jurisdiction reports complete laboratory data needed to identify stage of infection, data from most jurisdictions show that many of these cases were classified as Stage 0 (7.9%) or Stage 3 (20.2%) infection (i.e., cases diagnosed in early infection or late infection, respectively). Early and late diagnoses represent recent failures in prevention and testing systems, respectively, and opportunities to understand needed improvements in these systems. The NHSS classifies HIV infections as Stage 0 if the first positive HIV test was within six months of a negative HIV test. Persons who received a diagnosis at Stage 0 (i.e., early diagnosis) were able to access HIV testing shortly after infection yet were unable to benefit from biomedical and behavioral interventions to prevent HIV infection. The federal Ending the HIV Epidemic in the U.S. (EHE) initiative prioritizes the provision of HIV preexposure prophylaxis (PrEP), syringe services programs, treatment as prevention efforts, and other proven interventions—as part of the Prevent pillar of the EHE initiative—to prevent new HIV infections. HIV infections are classified as Stage 3 (AIDS) by the presence of an AIDSdefining opportunistic infection or by the lowest CD4 lymphocyte test result. Persons with Stage 3 infection at the time of their initial HIV diagnosis (i.e., late diagnosis) did not benefit from timely receipt of testing or HIV prevention interventions and were likely unaware of their infection for a substantial time. Nationally, an estimated 13.3% of persons with HIV are unaware of their infection, contributing to an estimated 40% of all ongoing transmission. Increasing early diagnosis is a crucial pillar of efforts to end HIV in the United States. Given the continued occurrence of HIV infections in the United States, the barriers and gaps associated with low uptake of HIV testing and prevention services must be addressed to reduce new infections and facilitate timely diagnosis and treatment. Therefore, CDC is sponsoring this data collection to improve understanding of barriers and gaps associated with new infection and late diagnosis in the era of multiple testing E:\FR\FM\06OCN1.SGM 06OCN1

Agencies

[Federal Register Volume 88, Number 193 (Friday, October 6, 2023)]
[Notices]
[Pages 69638-69640]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-22271]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[30Day-24-23AQ]


Agency Forms Undergoing Paperwork Reduction Act Review

    In accordance with the Paperwork Reduction Act of 1995, the Centers 
for Disease Control and Prevention (CDC) has submitted the information 
collection request titled ``Understanding HIV/STD Risk and Enhancing 
PrEP Implementation Messaging in a Diverse Community-Based Sample of 
Gay, Bisexual, and Other Men Who Have Sex with Men in a 
Transformational Era (MIC-DROP)'' to the Office of Management and 
Budget (OMB) for review and approval. CDC previously published a 
``Proposed Data Collection Submitted for Public Comment and 
Recommendations'' notice on November 16, 2022, to obtain comments from 
the public and affected agencies. CDC received two comments related to 
the previous notice. This notice serves to allow an additional 30 days 
for public and affected agency comments.
    CDC will accept all comments for this proposed information 
collection project. The Office of Management and Budget is particularly 
interested in comments that:
    (a) Evaluate whether the proposed collection of information is 
necessary for the proper performance of the functions of the agency, 
including whether the information will have practical utility;
    (b) Evaluate the accuracy of the agencies estimate of the burden of 
the proposed collection of information, including the validity of the 
methodology and assumptions used;
    (c) Enhance the quality, utility, and clarity of the information to 
be collected;
    (d) Minimize the burden of the collection of information on those 
who are to respond, including, through the use of appropriate 
automated, electronic, mechanical, or other technological collection 
techniques or other forms of information technology, e.g., permitting 
electronic submission of responses; and
    (e) Assess information collection costs.
    To request additional information on the proposed project or to 
obtain a copy of the information collection plan and instruments, call 
(404) 639-7570. Comments and recommendations for the proposed 
information collection should be sent within 30 days of publication of 
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular 
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function. Direct 
written comments and/or suggestions regarding the items contained in 
this notice to the Attention: CDC Desk Officer, Office of Management 
and Budget, 725 17th Street NW, Washington, DC 20503 or by fax to (202) 
395-5806. Provide written comments within 30 days of notice 
publication.

Proposed Project

    ``Understanding HIV/STD Risk and Enhancing PrEP Implementation 
Messaging in a Diverse Community-Based Sample of Gay, Bisexual, and 
Other Men Who Have Sex with Men in a Transformational Era (MIC-
DROP)''--New--National Center for HIV, Viral Hepatitis, STD, TB 
Prevention (NCHHSTP), Centers for Disease Control and Prevention (CDC).

Background and Brief Description

    CDC is requesting approval for three years for a data collection 
titled ``Understanding HIV/STD Risk and Enhancing PrEP Implementation 
Messaging in a Diverse Community-Based Sample of Gay, Bisexual, and 
Other Men Who Have Sex with Men in a Transformational Era (MIC-DROP).'' 
The purpose of the information collection is to understand men's 
strategies to prevent HIV and sexually transmitted infections (STIs), 
including preexposure prophylaxis (PrEP) use and adherence, condom use, 
sexual risk-taking behavior, and substance-using behaviors. This study 
will assess men's use and preferences for prevention modalities and 
their awareness, knowledge, beliefs, and perceptions about products 
that prevent the transmission of HIV and other sexually transmitted 
diseases (STD). This study will also conduct structured assessments to 
identify HIV prevention gaps and test prevention messages for men who 
have sex with men (MSM).
    The information collected in this study will be used to: (1) 
describe real-world HIV and STI prevention strategies including PrEP 
and condom use and

[[Page 69639]]

adherence; (2) better understand men's use, preferences, knowledge, and 
perceptions about prevention modalities; (3) develop rapid reports that 
will allow for summary recommendations concerning gaps in prevention 
protection and message testing; and (4) provide timely new information 
to public health programs and decision makers. The study will be 
carried out in three cities: Atlanta, GA; Chicago, IL; and San Diego, 
CA. Participants will include 1,275 HIV-negative men ages 18 and older. 
Cohort participants will identify as cisgender male; report sex with a 
man in the last six months; and be fluent in written/spoken English or 
Spanish. We will use purposive sampling to ensure that 60% of 
participants will be PrEP users at baseline, and 40% will not be using 
PrEP at that point. We will also oversample Black/African American and 
Hispanic/Latino MSM to ensure that a minimum of 30% each are 
represented in the cohort sample. Participants will be recruited using 
a combination of approaches including social media, referral, and in-
person outreach.
    A computer-assisted quantitative assessment will collect 
information about participants' use of prevention modalities, as well 
as their awareness, knowledge, beliefs, and perceptions about HIV/STI 
prevention products and prevention messages. The study will utilize the 
SMaRT (Study Management and Retention Toolkit) system, a study 
management platform for participant management that includes a HIPPA-
compliant companion mobile app that study participants install on their 
smart phones. The app supports several key functions of study 
participation including notifications of surveys available, 
administration of surveys, a messaging center, appointment scheduling, 
secure HIPPA-compliant document upload and return of laboratory 
results, and a HIPPA-compliant telehealth video conference platform. At 
six-month intervals starting at baseline, all participants will be 
mailed self-collection kits to provide samples for HIV and STI testing. 
Specimens for STI testing include urine, rectal, and pharyngeal swabs 
for gonorrhea and chlamydia and dried blood spot (DBS) for syphilis 
testing. HIV kits will collect DBS for 4th generation HIV testing. 
Tests will be shipped from, returned to, and processed by a CLIA-
certified laboratory. Participants will also have the option to self-
collect their specimens at a study site, where study staff will provide 
them with a self-collection kit and a private room in which to collect 
their specimens. A subset of the participant cohort will be invited to 
further participate in qualitative data collection activities including 
focus groups and in-depth interviews. The focus groups will assess the 
participants' awareness of PrEP messages, preferences for PrEP 
messages, and perceived impact/efficacy of HIV prevention and PrEP 
messages. The in-depth interviews will assess men's PrEP experiences, 
their preferences for PrEP and other HIV prevention products, and 
further explore their reactions to prevention messages. Participants 
will have the option to join virtual or in-person focus groups and 
interview sessions.
    Total study enrollment is 1,275 over the three-year data collection 
period. Based on screening and enrollment numbers from similar studies, 
we estimate we will need to screen 2,550 individuals (850 annually) to 
reach total enrollment. The screening process will take approximately 
five minutes to complete. Participants will be rescreened at the time 
of the enrollment visit. Contact information will be collected from 
1,275 participants (425 annually) and will take approximately five 
minutes to complete. The quantitative assessment will take 45 minutes 
to complete and will be delivered to 1,275 participants (850 annually) 
a total 8 times. The SMaRT app install will take 10 minutes to complete 
and will be completed by 1,275 participants (425 annually). The 
specimen kit for HIV testing will take approximately 20 minutes to 
complete and will be distributed to 1,275 participants (850 annually) a 
total of four times. The specimen kit for STI testing will take 
approximately 30 minutes to complete and will be distributed to 1,275 
participants (850 annually) a total of four times. A subset of the 
cohort participants will be invited to participate in qualitative data 
collection activities. A total of 144 participants (48 annually) will 
engage in a focus group that is estimated to take 90 minutes to 
complete, and 45 participants will be invited to participate in a 
series of three in-depth interviews to be administered at six-month 
intervals. The interviews will take approximately 60 minutes to 
complete.
    CDC is requesting 12,996 total burden hours across 3 years of data 
collection. The total estimated annualized burden hours are 4,332. 
Total burden for each activity has been rounded to the nearest whole 
hour. Participation of respondents is voluntary. There is no cost to 
participants other than their time.

                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                                      Average
                                                                     Number of       Number of      burden per
          Type of respondent                    Form name           respondents    responses per   response (in
                                                                                    respondent          hr)
----------------------------------------------------------------------------------------------------------------
General Public--Adults................  Eligibility Screener....             850               2            5/60
General Public--Adults................  Locator Form............             425               1            5/60
General Public--Adults................  Quarterly Assessment....             850               4           45/60
General Public--Adults................  SMaRT App Installation..             425               1           10/60
General Public--Adults................  Sample Collection for                850               2           20/60
                                         HIV Test.
General Public--Adults................  Sample Collection for                850               2           30/60
                                         STI Test.
General Public--Adults................  Focus Group.............              48               1           90/60
General Public--Adults................  In-Depth interview......              45               1           60/60
----------------------------------------------------------------------------------------------------------------



[[Page 69640]]

Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Public Health 
Ethics and Regulations, Office of Science, Centers for Disease Control 
and Prevention.
[FR Doc. 2023-22271 Filed 10-5-23; 8:45 am]
BILLING CODE 4163-18-P
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