OMB ICR Supporting Statement A and B - PRC FINAL 4.5.22

OMB ICR Supporting Statement A and B - PRC FINAL 4.5.22.docx

Indian Health Service Purchased/Referred Care Proof of Residency

OMB: 0917-0040

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Indian Health Service

Purchased/Referred Care Proof of Residency





Supporting Statement A and B


Justification


OMB Control No. 0917- 0040






















A.1. Circumstances Making the Collection of Information Necessary

The IHS Purchased/Referred Care Program needs the information requested on the PRC Proof of Residency form to verify that individuals seeking medical services through a PRC program meet the residency requirements specific to PRC under 42 C.F.R. § 136.23.


This is a request for information collection on a 3-year renewal information collection activity, 0917-0040, “Indian Health Service (IHS) Purchased/Referred Care Proof of Residency.” The Snyder Act (25 U.S.C. 13), the Transfer Act (Public Law 83-568, 42 U.S.C. 2001) and the IHS Regulations at 42 CFR Part 136, Subpart C authorize the IHS to contract for health care services for American Indian and Alaska Native (AI/AN) people eligible to receive such care.


A.2. Purpose and Use of the Information Collection

The form, “Purchased/Referred Care Proof of Residency” will serve as an alternative means to document Purchased/Referred Care (PRC) patient’s residency within an IHS Purchased/Referred Care delivery area (PRCDA), in accordance with the Purchased/Referred Care eligibility regulations at 42 CFR 136.23.


Individuals who may be potentially eligible for IHS PRC services complete the majority of the information contained on this form. The individuals and/or designated alternate complete and sign the streamlined form and submit it, along with the requested documents, to IHS for verification and eligibility determination.


The information collected is needed to administer and manage the PRC program to provide services to eligible AI/AN patients. The form is used 1) to request information regarding residency of individuals seeking medical services through PRC, 2) to verify that the individual meets the residency requirements specific to PRC under 42 C.F.R. § 136.23 using the information provided in response, and 3) to ensure submitted documents have been researched and verified to process eligibility of residence. The documents provided will serve as legal documentation of an individual’s residency within an IHS PRCDA.


The information collected is for planning for further care of the patient; for keeping an accurate record of the patient’s residency status; for planning future health care programs; for communicating among members of the health care team; and for the provision of program health statistics.


A.3. Use of Improved Information Technology and Burden Reduction

As appropriate, the IHS referral care information system and other automated information technology will be used to collect and process this data; however, currently the most appropriate methodology for obtaining the information is written responses on an information collection form. An electronic form has been developed as an option for the individual to download and fill-in. The method from processing responses will be captured on the form.


A.4. Efforts to Identify Duplication and Use of Similar Information

Duplication is not a problem. The required residency data is not available to IHS from any systems of other agencies. This information collection is part of the initial process for an individual to establish residency documentation for the IHS PRC Program. Only the IHS can initiate the proof of residency form, and this is the only form completed by each individual for the purposes of documenting residency.


A.5. Impact on Small Businesses or Other Small Entities

The collection of this information does not directly impact small businesses or small entities.


A.6. Consequences of Collecting the Information Less Frequently

Residency within a PRCDA is a requirement for eligibility under the federal regulations governing PRC. If this information was not documented, or was collected less frequently, the functions described in item 2 above would be curtailed.


A.7. Special Circumstances Relating to the Guidelines of 5 C.F.R 1320.5

There are no special circumstances relating to these guidelines. This request fully complies with the regulation.


A.8. Comments in Response to the Federal Register Notice and Efforts to Consult Outside the Agency


A 60-day notice Federal Register Notice was published in the Federal Register on

January 24, 2022, 87 FR 3562. There were no comments received. The 30-day notice is a reinstatement notice sending any comments received to OMB (87 FR 21181) published on April 22, 2022.


A.9. Explanation of Any Payment or Gift to Respondents

No payment or gift to respondents has been or will be made.


A.10. Assurance of Confidentiality Provided to Respondents

The information collected is maintained as part of Privacy Act System of Records,

09-17-0001, Medical, Health and Billing Records Systems, HHS/IHS/OHP, published in Privacy Act Issuances, 2006 Compilation, online via GPO Access. A Privacy Act Notification Statement is contained in the subject form.


A.11. Justification of Sensitive Questions


This collection does not address any matters of a sensitive nature.


A.12. Estimates of Annualized Burden Hours and Costs


Table A-3. Estimated Annualized Burden Hours

Type of Respondent

Form Name

No. of Respondents

No. Responses per Respondent

Average Burden per Response (hours)*

Total Burden

(hours)

Individual

User Count

77,185

1

3/60

3,859.25







Total

-

77,185

1

3/60

3,859.25

*For ease of understanding, the average burden per response is 3 minutes.


Table A-4 lists the estimated annualized burden costs.


Table A-4. Estimated Annualized Burden Costs

Type of

Respondent


Total Burden

Hours


Hourly

Wage Rate


Total Respondent Costs


Individual

3,859.25

0

0





Total

3,859.25

0

0


A.13. Estimates of Other Total Annual Cost Burden to Respondents and Record Keepers


There is no anticipated cost burden to the respondents resulting from this collection of information, except the costs associated with their time. There are no capital/startup costs associated with this collection of information.



A.14. Annualized Cost to the Federal Government


There will be no annual cost to the Federal government.


A.15. Explanation of Program Changes or Adjustments



There are no program changes or adjustments. This is a previously approved collection.



A.16. Plan for Tabulation, Publication, and Project Time Schedule


There are no plans to publish data from this information collection.


A.17. Reason Display of OMB Expiration Date is Inappropriate

Display of the OMB expiration date is appropriate and will be placed on all forms.

A.18. Exceptions to Certification for Paperwork Reduction Act Submissions


There are no exceptions to the certification.

This section is not mandatory


B.1. Respondent Universe and Sampling Methods


B.2. Procedures for the Collection of Information

B.3. Methods to Maximize Response Rates and Deal with Nonresponse



B.4. Tests of Procedures or Methods to be Undertaken

B.5. Individuals Consulted on Statistical Aspects and Individuals Collecting and Analyzing Data








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File TitleNational Survey of Lead Hazards in Housing
AuthorLillian L. Deitzer
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File Created2022-05-17

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