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
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.
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.