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Federal Register / Vol. 86, No. 39 / Tuesday, March 2, 2021 / Notices
FEDERAL RESERVE SYSTEM

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

Formations of, Acquisitions by, and Mergers of Bank Holding Companies
Agency for Healthcare Research and Quality
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The companies listed in this notice have applied to the Board for approval, pursuant to the Bank Holding Company Act of 1956 12 U.S.C. 1841 et seq.
BHC Act, Regulation Y 12 CFR part 225, and all other applicable statutes and regulations to become a bank holding company and/or to acquire the assets or the ownership of, control of, or the power to vote shares of a bank or bank holding company and all of the banks and nonbanking companies owned by the bank holding company, including the companies listed below.
The public portions of the applications listed below, as well as other related filings required by the Board, if any, are available for immediate inspection at the Federal Reserve Banks indicated below and at the offices of the Board of Governors.
This information may also be obtained on an expedited basis, upon request, by contacting the appropriate Federal Reserve Bank and from the Boards Freedom of Information Office at https www.federalreserve.gov/foia/
request.htm. Interested persons may express their views in writing on the standards enumerated in the BHC Act 12 U.S.C. 1842c.
Comments regarding each of these applications must be received at the Reserve Bank indicated or the offices of the Board of Governors, Ann E.
Misback, Secretary of the Board, 20th Street and Constitution Avenue NW, Washington DC 205510001, not later than April 1, 2021.
A. Federal Reserve Bank of Richmond Adam M. Drimer, Assistant Vice President 701 East Byrd Street, Richmond, Virginia 23219. Comments can also be sent electronically to or Comments.applications@rich.frb.org:
1. National Capital Bancorp, Inc., Washington, DC; to become a bank holding company by acquiring The National Capital Bank of Washington, Washington, DC.
Board of Governors of the Federal Reserve System, February 25, 2021.
Michele Taylor Fennell, Deputy Associate Secretary of the Board.
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Supplemental Evidence and Data Request on Improving Rural Health Through Telehealth-Guided Providerto-Provider Communication Agency for Healthcare Research and Quality AHRQ, HHS.
ACTION: Request for supplemental evidence and data submissions.
AGENCY:

The Agency for Healthcare Research and Quality AHRQ is seeking scientific information submissions from the public. Scientific information is being solicited to inform our review on Improving Rural Health Through Telehealth-Guided Provider-to-Provider Communication, which is currently being conducted by the AHRQs Evidence-based Practice Centers EPC
Program. Access to published and unpublished pertinent scientific information will improve the quality of this review.
DATES: Submission Deadline on or before April 1, 2021.
ADDRESSES:
Email submissions: epc@
ahrq.hhs.gov.
Print submissions:
Mailing Address: Center for Evidence and Practice Improvement, Agency for Healthcare Research and Quality, ATTN: EPC SEADs Coordinator, 5600
Fishers Lane, Mail Stop 06E53A, Rockville, MD 20857
Shipping Address FedEx, UPS, etc.:
Center for Evidence and Practice Improvement, Agency for Healthcare Research and Quality, ATTN: EPC
SEADs Coordinator, 5600 Fishers Lane, Mail Stop 06E77D, Rockville, MD 20857
FOR FURTHER INFORMATION CONTACT:
Jenae Benns, Telephone: 3014271496
or Email: epc@ahrq.hhs.gov.
SUPPLEMENTARY INFORMATION: The Agency for Healthcare Research and Quality has commissioned the Evidence-based Practice Centers EPC
Program to complete a review of the evidence for Improving Rural Health Through Telehealth-Guided Provider-toProvider Communication. AHRQ is conducting this systematic review pursuant to Section 902 of the Public Health Service Act, 42 U.S.C. 299a.
The EPC Program is dedicated to identifying as many studies as possible that are relevant to the questions for each of its reviews. In order to do so, we are supplementing the usual manual SUMMARY:

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and electronic database searches of the literature by requesting information from the public e.g., details of studies conducted. We are looking for studies that report on Improving Rural Health Through Telehealth-Guided Provider-toProvider Communication, including those that describe adverse events.
Telehealth for this review of providerto-provider communication is defined as any telecommunications facilitated interaction among, or support for, healthcare professionals designed to improve access, quality of care, or health outcomes for rural patients and populations. This includes a wide range of clinical applications such as remote ICU management; consultations for inpatient and outpatient care; and remote rounds or group education and case review e.g., Project ECHO, etc..
The entire research protocol is available online at: https
effectivehealthcare.ahrq.gov/products/
rural-telehealth/protocol.
This is to notify the public that the EPC Program would find the following information on Improving Rural Health Through Telehealth-Guided Provider-toProvider Communication helpful:
D A list of completed studies that your organization has sponsored for this indication. In the list, please indicate whether results are available on ClinicalTrials.gov along with the ClinicalTrials.gov trial number.
D For completed studies that do not have results on ClinicalTrials.gov, a summary, including the following elements: Study number, study period, design, methodology, indication and diagnosis, proper use instructions, inclusion and exclusion criteria, primary and secondary outcomes, baseline characteristics, number of patients screened/eligible/enrolled/lost to follow-up/withdrawn/analyzed, effectiveness/efficacy, and safety results.
D A list of ongoing studies that your organization has sponsored for this indication. In the list, please provide the ClinicalTrials.gov trial number or, if the trial is not registered, the protocol for the study including a study number, the study period, design, methodology, indication and diagnosis, proper use instructions, inclusion and exclusion criteria, and primary and secondary outcomes.
D Description of whether the above studies constitute ALL Phase II and above clinical trials sponsored by your organization for this indication and an index outlining the relevant information in each submitted file.
Your contribution is very beneficial to the Program. Materials submitted must be publicly available or able to be made public. Materials that are considered
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