Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT03136471 |
Other study ID # |
16-906810 |
Secondary ID |
|
Status |
Completed |
Phase |
|
First received |
|
Last updated |
|
Start date |
January 2017 |
Est. completion date |
March 1, 2021 |
Study information
Verified date |
March 2023 |
Source |
Tulane University |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational
|
Clinical Trial Summary
Investigators propose to use a natural experiment design to examine the impacts of the new
CPT code (99490) for chronic care management on health outcomes. The Investigators will
collaborate with partners in the Louisiana Clinical Data Research Network (LaCDRN) who serve
more than 90,000 patients with type 2 diabetes mellitus in Louisiana to examine impacts of
the CMS reimbursed care coordination. Now, LaCDRN is renamed as Research Action for Health
Network (REACHnet). Patient and stakeholder engagement will be planned and implemented across
all phases of this natural experiment. This project will examine outcome differences created
by the policy change in a natural experiment framework. The analyses will utilize the RE-AIM
framework to identify the critical elements of the programs that will enhance the reach,
effectiveness, adoption, implementation, and maintenance of these strategies in the diverse
LaCDRN diabetes populations.
PCORI Proposal COVID-19- Related Enhancement for Existing Research:
The proposed enhancement will contribute timely information to address two important
implications of the coronavirus pandemic:
1. Disparities in continuity of care and
2. Health systems' responsiveness in terms of telehealth delivery for high risk
populations.
The enhancement builds upon our current project by further examining effects of CMS payment
innovations to expand remotely delivered care. Our proposed study is a rapid assessment of
telehealth services, using an existing "learning health system" infrastructure to provide
timely, actionable evidence to inform telehealth service provision during the pandemic and
recovery.
Description:
The first aim is to evaluate the barriers and facilitators for the RE-AIM dimensions as
related to the new CMS chronic care management code overall and within each of the health
systems. The qualitative study will be used. Focus group interview will be conducted among
patients, healthcare professionals and stakeholders. A variety of qualitative techniques will
be used to collect data using key informant interviews among organization leaders of LaCDRN
partners to assess the organizational cultures, their social architecture, resources,
capacity, and communication networks. Face-to-face semi-structured interviews will be used to
explore these domains, assess barriers, and refine the data collection for the assessing the
RE-AIM framework. Further, semi-structured interviews will provide data to inform the
refinement of study outcomes and ensure organizational, cultural, and health-literacy
appropriateness. Focus groups will be audiotaped with the written consent of each
participant, and each tape will be transcribed verbatim and transcripts will be reviewed and
edited by the facilitators for accuracy. Inter-coder reliability will be examined. Interview
transcripts will be imported into NVivo 10 software (QSR International, Burlington, MA).
Codes and concepts identified in preliminary review will be refined, extended, and
cross-referenced. Coded texts will be structured into taxonomies and transformed into a
matrix format so that responses and concepts can be compared across respondent groups.
Finally, taxonomies and matrices will be summarized by similarities and contrasts to form
overarching themes and dimensions. We will use an iterative technique until theoretical
saturation, the point at which no additional major themes emerge, is reached. Diabetes care
coordination readiness assessment will be conducted with LaCDRN partner health system's
medical directors (organizational).
The second one is the health and economic impacts of the NFFCCM to improve health outcomes:
glycemic control, CVD risk reduction, medication adherence, patient-reported outcomes (PRO),
and health care utilization. Data extraction from the REACHnet. De-identified data from EMR
includes birth year, gender, race, state of residency, zip-codes, medical history, lab
results and prescriptions. All data comply with the Health Insurance Portability and
Accountability Act (HIPAA).
This proposed research is significant because it is the first natural experiment to test an
ongoing CMS reimbursement policy on diabetes care in Louisiana. The study questions and study
outcomes will be patient-centered, and will generate urgently needed data on effective,
practical, and sustainable population-targeted strategies aimed at reducing diabetes-related
disease burden in Medicare-eligible populations. Further dissemination and scale-up efforts
will create large return on multiple health systems and non-CMS populations.
PCORI Proposal COVID-19- Related Enhancement for Existing Research Aims:
Aim1: Examine facilitators and barriers to uptake, adoption, and implementation of telehealth
services among Medicare patients with diabetes from health systems', providers' and patients'
perspectives. With the substantial increase in telehealth encounters starting in early March
2020, we hypothesize disparities in adoption and implementation of telehealth at health
system, provider and patient levels. For example, our current project has identified
significant variations in NFFCCM implementation across three health systems in Louisiana. For
the enhancement, we intend to examine variations in health systems' implementation of
Medicare-reimbursable telehealth services, which may not mirror the variations we observed
for NFFCCM given the dramatically different context of the current pandemic.
Aim 2: Compare diabetes control and continuity of care between patients with and without
utilization of telehealth. We hypothesize better diabetes management among Medicare patients
with telehealth versus without.