Agency Information Collection Activities: Proposed Collection; Comment Request, 41619-41620 [2023-13579]

Download as PDF Federal Register / Vol. 88, No. 122 / Tuesday, June 27, 2023 / Notices • EXCLUDE: Single group (noncomparative) studies, including case reports or series • EXCLUDE: Studies with N<10 per arm • EXCLUDE: Studies published only in dissertation or conference abstract format DEPARTMENT OF HEALTH AND HUMAN SERVICES We will collect SRs to identify potentially eligible primary studies (within date restrictions) and possibly to narratively summarize older studies of earlier foundational nonpharmacological interventions. For topics with robust existing SRs (e.g., non-pharmacological interventions for perinatal depression), we will consider (with partners and our task order officer [TOO]) updating these SRs (relying on the published SRs for all data pertaining to the older primary studies). Eligibility criteria specific to Key Question 1 (nonpharmacologic vs. nothing/treatment as usual/usual care or vs. other nonpharmacologic) AGENCY: Intervention • May include same pharmacologic cointervention as comparator group Comparators • No nonpharmacologic treatment • Other nonpharmacologic modality • May include same pharmacologic cointervention as intervention group Eligibility criteria specific to Key Question 2 (nonpharmacologic vs pharmacologic) Intervention • Nonpharmacologic intervention alone (no use of pharmacologic therapy) Comparators • Pharmacologic treatment alone Dated: June 21, 2023. Marquita Cullom, Associate Director. [FR Doc. 2023–13581 Filed 6–26–23; 8:45 am] ddrumheller on DSK120RN23PROD with NOTICES1 BILLING CODE 4160–90–P VerDate Sep<11>2014 18:54 Jun 26, 2023 Jkt 259001 Agency for Healthcare Research and Quality Agency Information Collection Activities: Proposed Collection; Comment Request Agency for Healthcare Research and Quality, HHS. ACTION: Notice. This notice announces the intention of the Agency for Healthcare Research and Quality (AHRQ) to request that the Office of Management and Budget (OMB) approve the proposed information collection project ‘‘Use of Open-Ended Responses to Explore Disparities in Patient Experience.’’ The purpose of this notice is to allow 60 days for public comment. DATES: Comments on this notice must be received by August 28, 2023. ADDRESSES: Written comments should be submitted to: Doris Lefkowitz, Reports Clearance Officer, AHRQ, by email at doris.lefkowitz@AHRQ.hhs.gov. FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ Reports Clearance Officer, (301) 427–1477, or by email at doris.lefkowitz@AHRQ.hhs.gov. SUPPLEMENTARY INFORMATION: SUMMARY: Proposed Project Use of Open-Ended Responses To Explore Disparities in Patient Experience The Consumer Assessment of Healthcare Providers and Systems (CAHPS) program, which is sponsored by AHRQ, has the purpose of advancing the scientific understanding of the patient experience of care, including the development and testing of new surveys and/or approaches to data collection to promote or improve the collection of consumer reports and evaluations of their experiences with health care. This Project has the following goals: (1) Use open-ended (narrative) responses to provide context, detail, and understanding regarding observed differences in patient experience based on race, ethnicity, gender, and preferred language. (2) Use Clinician and Group -CAHPS Narrative Item Set (NIS)-generated narrative data to examine potential PO 00000 Frm 00034 Fmt 4703 Sfmt 4703 41619 algorithmic bias in natural language programs (NLP) that could potentially be used to code large quantities of narrative data. (3) Where algorithmic bias is uncovered, use this analysis to identify adjustments that can be applied to both the input for these programs or the outputs. This project is being conducted by AHRQ through its contractor, the RAND Corporation, pursuant to AHRQ’s statutory authority to conduct and support research on health care and on systems for the delivery of such care, including activities with respect to the quality, effectiveness, efficiency, appropriateness, and value of healthcare services and with respect to quality measurement and improvement. 42 U.S.C 299a(a)(1) and (2). Method of Collection To achieve the goals of this project the following data collections will be implemented: Online survey: Data will be collected from a sample of 4,998 survey respondents drawn from the Ipsos KnowledgePanel, a large nationwide online panel of American adults (over 50,000 panelists) with demographic characteristics consistent with the adult U.S. population. Equal-sized subsamples will be drawn for each of the following groups: non-Hispanic Asian American, Native Hawaiian or Other Pacific Islander; non-Hispanic Black; Spanish-speaking Hispanic; English-speaking Hispanic; nonHispanic Multiracial; and non-Hispanic White. Within these six subsamples, we will strive to recruit a roughly equal split of men and women. The survey will be fielded in English and Spanish based on respondent-preferred language. Estimated Annual Respondent Burden Exhibit 1 shows the estimated annualized burden hours for survey respondents’ time to participate in this data collection. All participants will complete the Online Survey, which is estimated to take 17 minutes per response. The total annual burden hours are estimated to be 1,416 hours. Exhibit 2 shows the estimated annualized cost burden associated with the respondents’ time to participate in this data collection. The cost burden is estimated to be $39,662. E:\FR\FM\27JNN1.SGM 27JNN1 41620 Federal Register / Vol. 88, No. 122 / Tuesday, June 27, 2023 / Notices EXHIBIT 1—ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Form name Number of responses per respondent Hours per response Total burden hours Online Survey .................................................................................................. 4,998 1 .28 1,416 Total .......................................................................................................... 4,998 na na 1,416 EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN Number of respondents Form name Total burden hours Average hourly wage rate * Total cost burden Online Survey .................................................................................................. 4,998 1,416 a $28.01 $39,662 Total .......................................................................................................... 4,998 1,416 Na $39,662 * The May 2017 National Employment and Wage Estimates reported by the Bureau of Labor statistics indicate an average hourly wage of $28.01 across the 50 U.S. states and the District of Columbia. The national average has been used to estimate the wages of survey respondents. The Knowledge Panel consists of a broad cross-section of the U.S. adult population, and thus a national average should be a reasonable estimate of the wages of survey respondents. National Compensation Survey: Occupational wages in the United States May 2021, ‘‘U.S. Department of Labor, Bureau of Labor Statistics.’’ a Based on the mean wages for all occupations, code 00–0000. Request for Comments ddrumheller on DSK120RN23PROD with NOTICES1 In accordance with the Paperwork Reduction Act, 44 U.S.C. 3501–3520, comments on AHRQ’s information collection are requested with regard to any of the following: (a) whether the proposed collection of information is necessary for the proper performance of AHRQ’s health care research and health care information dissemination functions, including whether the information will have practical utility; (b) the accuracy of AHRQ’s estimate of burden (including hours and costs) of the proposed collection(s) of information; (c) ways to enhance the quality, utility and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information upon the respondents, including the use of automated collection techniques or other forms of information technology. Comments submitted in response to this notice will be summarized and included in the Agency’s subsequent request for OMB approval of the proposed information collection. All comments will become a matter of public record. Dated: June 21, 2023. Marquita Cullom, Associate Director. [FR Doc. 2023–13579 Filed 6–26–23; 8:45 am] BILLING CODE 4160–90–P VerDate Sep<11>2014 18:54 Jun 26, 2023 Jkt 259001 DEPARTMENT OF HEALTH AND HUMAN SERVICES Agency for Toxic Substances and Disease Registry [60Day–23–0057; Docket No. ATSDR–2023– 0002] Proposed Data Collection Submitted for Public Comment and Recommendations Agency for Toxic Substances and Disease Registry (ATSDR), Department of Health and Human Services (HHS). ACTION: Notice with comment period. AGENCY: The Agency for Toxic Substances and Disease Registry (ATSDR), 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 continuing information collection, as required by the Paperwork Reduction Act of 1995. This notice invites comment on a proposed information collection project titled APPLETREE Performance Measures. ATSDR will use this data collection to manage the next five-year cooperative agreement program under Notice of Funding Opportunity (NOFO) No. CDC– RFA–TS–23–0001. DATES: ATSDR must receive written comments on or before August 28, 2023. ADDRESSES: You may submit comments, identified by Docket No. ATSDR–2023– 0002 by either of the following methods: • Federal eRulemaking Portal: www.regulations.gov. Follow the instructions for submitting comments. SUMMARY: PO 00000 Frm 00035 Fmt 4703 Sfmt 4703 • 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. ATSDR will post, without change, all relevant comments to www.regulations.gov. Please note: Submit all comments through the Federal eRulemaking portal (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: 404–639–7570; 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 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 E:\FR\FM\27JNN1.SGM 27JNN1

Agencies

[Federal Register Volume 88, Number 122 (Tuesday, June 27, 2023)]
[Notices]
[Pages 41619-41620]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-13579]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Agency for Healthcare Research and Quality


Agency Information Collection Activities: Proposed Collection; 
Comment Request

AGENCY: Agency for Healthcare Research and Quality, HHS.

ACTION: Notice.

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

SUMMARY: This notice announces the intention of the Agency for 
Healthcare Research and Quality (AHRQ) to request that the Office of 
Management and Budget (OMB) approve the proposed information collection 
project ``Use of Open-Ended Responses to Explore Disparities in Patient 
Experience.'' The purpose of this notice is to allow 60 days for public 
comment.

DATES: Comments on this notice must be received by August 28, 2023.

ADDRESSES: Written comments should be submitted to: Doris Lefkowitz, 
Reports Clearance Officer, AHRQ, by email at 
[email protected].

FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ Reports 
Clearance Officer, (301) 427-1477, or by email at 
[email protected].

SUPPLEMENTARY INFORMATION: 

Proposed Project

Use of Open-Ended Responses To Explore Disparities in Patient 
Experience

    The Consumer Assessment of Healthcare Providers and Systems (CAHPS) 
program, which is sponsored by AHRQ, has the purpose of advancing the 
scientific understanding of the patient experience of care, including 
the development and testing of new surveys and/or approaches to data 
collection to promote or improve the collection of consumer reports and 
evaluations of their experiences with health care.
    This Project has the following goals:
    (1) Use open-ended (narrative) responses to provide context, 
detail, and understanding regarding observed differences in patient 
experience based on race, ethnicity, gender, and preferred language.
    (2) Use Clinician and Group -CAHPS Narrative Item Set (NIS)-
generated narrative data to examine potential algorithmic bias in 
natural language programs (NLP) that could potentially be used to code 
large quantities of narrative data.
    (3) Where algorithmic bias is uncovered, use this analysis to 
identify adjustments that can be applied to both the input for these 
programs or the outputs.
    This project is being conducted by AHRQ through its contractor, the 
RAND Corporation, pursuant to AHRQ's statutory authority to conduct and 
support research on health care and on systems for the delivery of such 
care, including activities with respect to the quality, effectiveness, 
efficiency, appropriateness, and value of healthcare services and with 
respect to quality measurement and improvement. 42 U.S.C 299a(a)(1) and 
(2).

Method of Collection

    To achieve the goals of this project the following data collections 
will be implemented:
    Online survey: Data will be collected from a sample of 4,998 survey 
respondents drawn from the Ipsos KnowledgePanel, a large nationwide 
online panel of American adults (over 50,000 panelists) with 
demographic characteristics consistent with the adult U.S. population. 
Equal-sized subsamples will be drawn for each of the following groups: 
non-Hispanic Asian American, Native Hawaiian or Other Pacific Islander; 
non-Hispanic Black; Spanish-speaking Hispanic; English-speaking 
Hispanic; non-Hispanic Multiracial; and non-Hispanic White. Within 
these six subsamples, we will strive to recruit a roughly equal split 
of men and women. The survey will be fielded in English and Spanish 
based on respondent-preferred language.

Estimated Annual Respondent Burden

    Exhibit 1 shows the estimated annualized burden hours for survey 
respondents' time to participate in this data collection. All 
participants will complete the Online Survey, which is estimated to 
take 17 minutes per response. The total annual burden hours are 
estimated to be 1,416 hours.
    Exhibit 2 shows the estimated annualized cost burden associated 
with the respondents' time to participate in this data collection. The 
cost burden is estimated to be $39,662.

[[Page 41620]]



                                  Exhibit 1--Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                     Number of
                    Form name                        Number of     responses per     Hours per     Total burden
                                                    respondents     respondent       response          hours
----------------------------------------------------------------------------------------------------------------
Online Survey...................................           4,998               1             .28           1,416
                                                 ---------------------------------------------------------------
    Total.......................................           4,998              na              na           1,416
----------------------------------------------------------------------------------------------------------------


                                   Exhibit 2--Estimated Annualized Cost Burden
----------------------------------------------------------------------------------------------------------------
                                                     Number of     Total burden   Average hourly    Total cost
                    Form name                       respondents        hours        wage rate *       burden
----------------------------------------------------------------------------------------------------------------
Online Survey...................................           4,998           1,416      \a\ $28.01         $39,662
                                                 ---------------------------------------------------------------
    Total.......................................           4,998           1,416              Na         $39,662
----------------------------------------------------------------------------------------------------------------
* The May 2017 National Employment and Wage Estimates reported by the Bureau of Labor statistics indicate an
  average hourly wage of $28.01 across the 50 U.S. states and the District of Columbia. The national average has
  been used to estimate the wages of survey respondents. The Knowledge Panel consists of a broad cross-section
  of the U.S. adult population, and thus a national average should be a reasonable estimate of the wages of
  survey respondents. National Compensation Survey: Occupational wages in the United States May 2021, ``U.S.
  Department of Labor, Bureau of Labor Statistics.''
\a\ Based on the mean wages for all occupations, code 00-0000.

Request for Comments

    In accordance with the Paperwork Reduction Act, 44 U.S.C. 3501-
3520, comments on AHRQ's information collection are requested with 
regard to any of the following: (a) whether the proposed collection of 
information is necessary for the proper performance of AHRQ's health 
care research and health care information dissemination functions, 
including whether the information will have practical utility; (b) the 
accuracy of AHRQ's estimate of burden (including hours and costs) of 
the proposed collection(s) of information; (c) ways to enhance the 
quality, utility and clarity of the information to be collected; and 
(d) ways to minimize the burden of the collection of information upon 
the respondents, including the use of automated collection techniques 
or other forms of information technology.
    Comments submitted in response to this notice will be summarized 
and included in the Agency's subsequent request for OMB approval of the 
proposed information collection. All comments will become a matter of 
public record.

    Dated: June 21, 2023.
Marquita Cullom,
Associate Director.
[FR Doc. 2023-13579 Filed 6-26-23; 8:45 am]
BILLING CODE 4160-90-P


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