This ICR was
approved for one-year because it is a one-time data
collection.
Inventory as of this Action
Requested
Previously Approved
09/30/2017
36 Months From Approved
50
0
0
100
0
0
0
0
0
A goal of Healthy People 2020 is to
increase Americans’ health literacy, defined as “the degree to
which individuals have the capacity to obtain, process, and
understand basic health information and services needed to make
appropriate health decisions.” 1 The effects of limited health
literacy are numerous and serious, including medication
non-adherence resulting from patients’ inability to read and
comprehend medication labels; under use of preventive measures,
such as vaccines; poor self-management of conditions such as asthma
and diabetes; and higher utilization of inpatient and emergency
department care. 2,3 According to the 2003 National Assessment of
Adult Literacy, 88% of US adults have significant difficulties
understanding widely used health information. 4 By adopting “health
literacy universal precautions,” health care providers and
organizations can create an environment in which all patients –
regardless of health literacy level – can successfully (1)
understand health information, (2) navigate the health care system,
(3) engage in medical decision-making, and (4) manage their health.
Numerous resources have been developed to support health care
organizations in their attempts to address limitations in patient
health literacy. 5 However, little work has been done to establish
valid quality improvement measures that organizations can use to
monitor the impact of initiatives aimed at improving patient
understanding, navigation, engagement, and self-management. Absent
such measures, organizations may be unable to accurately assess
whether their initiatives are effective. This research has the
following goals: 1. Identify existing quality improvement measures
and gather proposals for additional measures (not generated from
patient survey data) that organizations may use to monitor progress
related to enhancing patient understanding, navigation, engagement,
and self-management; and 2. Identify a set of quality improvement
measures that reflect patient priorities, has expert support, and
can be recommended for more formal measure development and
testing.
US Code:
42
USC 299 Name of Law: Healthcare Research and Quality Act of
1999
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.