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Using Remote Monitoring to Address Health Disparities in Type 2 Diabetes

L

Lawndale Christian Health Center

Status

Invitation-only

Conditions

Diabetes Mellitus, Type 2

Treatments

Other: Usual Care
Device: Continuous glucose monitor
Device: Blood glucose monitor with Digital Platform and Health Coaching

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06517576
P30DK092949 (U.S. NIH Grant/Contract)
LCHC-ID-10

Details and patient eligibility

About

Patient populations at community health centers, specifically Black or African American and Hispanic or Latino populations with Type 2 diabetes, experience significant health disparities. In particular, they have higher rates of diabetes-related complications and other related conditions such as myocardial infarction, cerebrovascular disease, kidney failure, blindness, neuropathy, and the risk of amputation. Diabetes affects 34 million adults in the US. Achieving a target HbA1c less than 8% can be challenging through diabetes management. Patients are able to monitor their blood glucose levels with devices such as blood glucose meters or continuous glucose monitors to facilitate diabetes management and glycemic control. Past studies have demonstrated that these devices are effective in engaging patients in the improvement of diabetes management. Current advancements in remote patient monitoring and self-monitoring have been observed to be effective in facilitating improvement in diabetes outcomes. However, the effectiveness and financial feasibility of these devices delivered in conjunction with automated patient engagement systems in remote patient monitoring programs is not well understood among underinsured, underserved, and vulnerable minority populations as they face a high-cost barrier particularly with continuous glucose monitors. To better address this gap in knowledge, this pilot study will compare and examine the effectiveness of these interventions on patient outcomes with Type 2 diabetes among populations in the West Side of Chicago. Study the comparative effectiveness among patients with uncontrolled Type 2 diabetes on insulin in an intervention group using remote patient monitoring and automated patient engagement system with blood glucose monitors to a group using a self-monitoring program with continuous glucose monitors and a usual care group receiving standard care. Conduct a feasibility analysis and financial impact of these programs among an underinsured and underserved population of Black/African Americans or Hispanic/Latinos with Type 2 diabetes.

Full description

This will be conducted at a Lawndale Christian Health Center, a community health center in the West Side of Chicago that serves a largely Black or African American and Hispanic or Latino population. To accomplish this objective, Aim 1 will study the impact on patients with uncontrolled Type 2 diabetes on insulin by comparing an intervention group that features remote patient monitoring with an automated patient engagement system and health coaching using blood glucose meters compared to a group that features a self-monitoring program using continuous glucose monitoring devices and a usual care group with standard care, and Aim 2 will examine the feasibility of implementing these interventions and financial impact of each treatment group at a community health center. To understand the effect of this study on health outcomes, patient level data will be examined including primary outcomes for health measurements such as HbA1c, blood glucose, BMI/weight, estimated glomerular filtration rate (eGFR), patient-reported outcomes including medication adherence, daily activities, diabetes self-management activities, and secondary outcomes for health measurements such as LDL cholesterol, systolic and diastolic blood pressures, as well as implementation outcomes such as acceptability, appropriateness, and feasibility. The costs of implementation and delivery will be examined using a budget impact analysis. This study will be essential for informing the impact on health disparities through remote monitoring with automated patient engagement compared to self-monitoring when providing care for underinsured and underserved populations.

Enrollment

150 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years of age or older
  • Have an assigned primary care provider
  • Diagnosis of Type 2 diabetes
  • Medication use is insulin
  • HbA1c of 8.0% or higher

Exclusion criteria

  • Diagnosis of chronic kidney disease at Stage 4 or higher
  • Diagnosis of pregnancy
  • Diagnosis of behavioral health conditions including serious mental illness or severe depression in the past 6 months.
  • All participants must have a smartphone that is able to access internet services.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

150 participants in 3 patient groups

Remote patient monitoring and automated patient engagement system with blood glucose monitors
Experimental group
Description:
Participants in this group will receive blood glucose monitors and will check their blood glucose daily with monitoring through a digital platform and provided health coaching.
Treatment:
Device: Blood glucose monitor with Digital Platform and Health Coaching
Self-monitoring program with continuous glucose monitors
Experimental group
Description:
Participants in this group will receive continuous glucose monitors and will self monitor their blood glucose measurements with support by their care team.
Treatment:
Device: Continuous glucose monitor
Usual care group receiving standard care
Active Comparator group
Description:
Participants in this group will receive standard care for diabetes.
Treatment:
Other: Usual Care

Trial contacts and locations

1

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Central trial contact

Andrew Wang, PhD, MPH; Catherine Lin, MD

Data sourced from clinicaltrials.gov

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