Beneficiary and Family Centered Data Collection (CMS-10393)

ICR 202010-0938-001

OMB: 0938-1177

Federal Form Document

Forms and Documents
Document
Name
Status
Supporting Statement B
2020-10-01
Supporting Statement A
2020-10-01
IC Document Collections
ICR Details
0938-1177 202010-0938-001
Received in OIRA 201707-0938-002
HHS/CMS CCSQ
Beneficiary and Family Centered Data Collection (CMS-10393)
Extension without change of a currently approved collection   No
Regular 10/01/2020
  Requested Previously Approved
36 Months From Approved 02/28/2021
9,100 24,970
2,191 2,899
11,375 31,213

To ensure the QIOs are effectively meeting their goals, CMS has historically collected patient experience information through a survey of beneficiaries who have interacted directly with a QIO representative. In this way, CMS assesses the degree to which the QIOs are achieving the above program requirements; provides feedback to the QIOs to support them in improving the services they deliver to Medicare beneficiaries; and measures the degree to which the QIOs are meeting their contractual obligations as laid out in their SOW. CMS must continue to collect reliable and rich data on the experiences of Medicare beneficiaries. The nature of the data collected must also evolve as QIO contract changes so that CMS is adequately capturing how, when, and why QIOs are interacting with beneficiaries and beneficiary reports on their related experiences.

US Code: 42 USC 1320c Name of Law: Functions of Peer Review Organizations
  
None

Not associated with rulemaking

  85 FR 43581 07/17/2020
85 FR 60798 09/28/2020
No

1
IC Title Form No. Form Name
Medicare Beneficiary and Family-Centered Satisfaction Survey CMS-10393, CMS-10393, CMS-10393 Attachment A: Beneficiary Experience Survey ,   Attachment C: General Feedback Web Survey ,   Attachment B: Direct Follow-up

  Total Request Previously Approved Change Due to New Statute Change Due to Agency Discretion Change Due to Adjustment in Estimate Change Due to Potential Violation of the PRA
Annual Number of Responses 9,100 24,970 0 0 -15,870 0
Annual Time Burden (Hours) 2,191 2,899 0 0 -708 0
Annual Cost Burden (Dollars) 11,375 31,213 0 0 -19,838 0
No
No
Total estimated burden for this request represents a decrease in burden hours from 2,899 (approach approved in February 2018 as OMB NO. 0938-1177) to 2,191. This is primarily the result of fewer beneficiaries to responding to the voluntarily available General Feedback Web Survey.

$1,816,287
No
    No
    No
No
No
No
No
Denise King 410 786-1013 Denise.King@cms.hhs.gov

  No

On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
 
 
 
 
 
 
 
    (i) Why the information is being collected;
    (ii) Use of information;
    (iii) Burden estimate;
    (iv) Nature of response (voluntary, required for a benefit, or mandatory);
    (v) Nature and extent of confidentiality; and
    (vi) Need to display currently valid OMB control number;
 
 
 
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.
10/01/2020


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