Spina bifida is one of the most common
birth defects, affecting approximately 3 per 10,000 live births in
the United States annually. Providing care for people who are born
with spina bifida is complex and challenging. Multiple physicians
and many other professionals and services are involved regularly in
addressing the many medical and non-medical issues that these
individuals and their families face. Care coordination has been
utilized for individuals with complex health conditions such as
cystic fibrosis and sickle cell anemia, and has been found to be
beneficial for assisting patients and their families. However, a
limited number of empirical studies have examined care coordination
within the spina bifida clinic setting. The proposed data
collection will use qualitative methods to 1) examine the extent to
which care coordination in spina bifida clinics is perceived to be
effective; 2) identify perceived barriers to providing care
coordination in spina bifida clinics; and 3) identify potential
best practices related to providing care coordination in spina
bifida clinics.
US Code:
42
USC 317C Name of Law: Birth Defects and Developmental
Disabilities Prevention Act of 2003
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.