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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03827902
Other study ID # STU 042018-008
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date July 9, 2019
Est. completion date April 2, 2020

Study information

Verified date November 2020
Source University of Texas Southwestern Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of the study is to compare whether an integrated model of care between Foot Wound and Diabetes Clinic with use of remote glucose monitoring technology (Intervention Arm), as compared with usual care without the use of remote glucose monitoring technology (Control Arm), will result in 1) improved glycemic control, 2) improved ulcer and wound healing, 3) improved patient reported outcomes (PROs), 4) reduced long-term healthcare resource utilization, and 5) improved adherence to anti-glycemic therapy for patients with DFUWI and poor glycemic control over the course of a 6-month intervention period.


Description:

This is a two-arm non-randomized convenient pilot trial to assess impact of an active glycemic management model through remote glucose monitoring technology amongst patients with DFUWI and poor glycemic control at the Parkland Diabetes Foot & Wound clinic. The plan is to implement a remote glucose monitoring technology to facilitate improved glycemic management and control. A cellular enabled glucose meter that will upload blood glucose measurements to a cloud server accessible by providers who can remotely review glycemic trends and remotely provide patients with proactive recommendations for treatment adjustments will be used. Patients receiving services in the integrated care model (same day visits in the Foot Wound and Diabetes Clinics at Parkland) will be eligible for inclusion in the intervention arm which includes proactive glucose monitoring guided by remote glucose monitoring technology. Patients receiving usual care services (non-integrated care model clinic days where Foot Wound and Diabetes Clinic visits are on separate days) will be eligible for inclusion in the control arm. The expectation is that patients in the intervention arm will experience greater improvements in glycemic control, compared to the usual care model. The hypothesis is that improved glycemic control in these patients will result in faster healing of diabetic foot wound, infections or ulcers. The effectiveness of the technologically facilitated integrated model of care will be evaluated compared to the usual care using metrics for diabetic foot ulcers and wound healing, glycemic control, patient reported outcomes, health resource utilization and medication adherence after 6 months of intervention. The Telcare 2.0 BGM for remote self-blood glucose monitoring(FDA Cleared) will be used.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date April 2, 2020
Est. primary completion date April 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Type 2 Diabetes - 18 years and older - A1C greater than or equal to 8.5% within the preceding 6 months - A1C greater than 8% on day of enrollment - Active diabetic foot ulcer or wound receiving treatment in the Foot Wound clinic at Parkland (ulcer that meets University of Texas Classification Grade 1 or 2 of any stage) Exclusion Criteria: - Chronic osteomyelitis (even if completed active therapy) - Moderate/severe lower limb infection (per Infectious Diseases Society of America criteria) - Diabetic Foot Ulcer and Wound Infection on Charcot Foot - Any serious/unstable medical condition that interferes with treatment assignment - Ankle Brachial Index less than 0.7 or toe pressures less than 30mmHg - Unwilling to participate or receive injectable treatment or unable to keep appointments - Non-English or Non-Spanish speakers - Pregnant or planning to become pregnant

Study Design


Intervention

Device:
Telcare 2.0 BGM
Blood glucose meter that uploads blood glucose measurements to a cloud server that providers can access and use to monitor patients' glycemic trends.

Locations

Country Name City State
United States Parkland Health and Hospital System Dallas Texas

Sponsors (2)

Lead Sponsor Collaborator
University of Texas Southwestern Medical Center Parkland Health & Hospital System

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Frequency of hypoglycemic events Comparison of frequency of severe hypoglycemic symptoms for usual care versus intervention arm 6 months
Primary Change in HbA1c Mean change in HbA1c from baseline to end of treatment 6 months
Secondary Glycemic control Proportion of patients with lower A1C and insulin use 6 months
Secondary Foot ulcer and/or wound healing Complete wound healing as defined by University of Texas Health System 6 months
Secondary Patient reported satisfaction with diabetes treatment Self-reported outcome assessment questionnaire using the Diabetes Treatment Satisfcation Questionnaire (DTSQ) [Scale range 0-48]; lower scores represent worse outcomes 6 months
Secondary Patient reported health status Self-reported outcome assessment questionnaires using the 5 level EQ-5D health status measure (EQ-5D-5L) [Scale range 5-25]; higher scores represent worse outcome 6 months
Secondary Proportion of patients with emergency department visits Proportion of patients with emergency department visits following enrollment 6 months
Secondary Proportion of days covered score Proportion of days covered score represents an indirect measure of medication adherence and represents the proportion of days medication was dispensed (numerator) over the total potential days the medication should have been dispensed (denominator) 6 months
Secondary Proportion of patients with hospitalization Proportion of patients with hospitalization following enrollment 6 months
Secondary Frequency of invasive procedures Total number and type of invasive procedures related to diabetic foot ulcer and or wound infection 6 months
Secondary Number of outpatient visits Total number of outpatient visits for general or specialized care (including virtual visits) during trial 6 months
Secondary Number of casts and boots used for treatment Total number of casts and boots used for treatment related to diabetic foot ulcer and or wound infection 6 months
Secondary Overall hospital incurred patient-specific cost Cost (in US $) of overall patient care for Parkland during study enrollment 6 months
Secondary Cost of glycemic management during study • Cost of glycemic management during trial, including cost of encounters (including telephone and virtual visits), testing supplies, drug costs, technology costs specifically related to glycemic management 6 months
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