Diabetes eConsult Non-Inferiority Study
- Conditions
- Diabetes
- Interventions
- Other: Standard of careOther: eConsult
- Registration Number
- NCT04089202
- Lead Sponsor
- Boston Medical Center
- Brief Summary
Flash glucose monitoring is an FDA-approved and widely clinically available, glucose monitoring technology that is worn on the body and measures glucose values every 15 minutes, storing this data for up to 14 days. The Freestyle Libre Pro is already used as a diagnostic technology in clinical care. It provides a full 24-hour glucose profile for each day that the sensor is worn and that can be correlated with daily activities, medication administration, food intake, and other factors that are contextually relevant in meeting glycemic goals for an individual patient.
In this study, patients referred to Endocrinology for specialty diabetes care will be randomized to an in-person visit as is typically done or to wear the Freestyle Libre Pro placed by staff at their primary care clinic. Patients who wear the Freestyle Libre Pro will have a professional interpretation of their glucose data completed by an endocrinologist as well as a remote eConsult completed using this glucose data and information from their medical record. The recommendations from the eConsult regarding medication and lifestyle adjustment as well as potential referral on to see Endocrinology will be implemented by the primary care physician at their clinical discretion.
The investigators will utilize glycemic measures including hemoglobin A1c, number of clinical visits (outpatient, inpatient and emergency department) for diabetes care, patient reported outcomes including self-efficacy, and patient and provider assessments of burden to determine if eConsults utilizing flash glucose monitoring technology are non-inferior to in-person visits with a diabetes specialist.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 87
- Male and female subjects age 18-80, inclusive
- Diagnosed with type 2 diabetes at least 6 months prior to screening
- Not previously seen within the prior three years in the endocrinology clinic for diabetes management
- Referred to endocrinology for diabetes care directly from primary care
- Willing to wear an Abbott® FreeStyle Libre Pro for 7-14 days
- English speaking
- Able and willing to complete questionnaires
- Planned travel or surgery during the time of libre wear
- Patients without a diagnosis of type 2 diabetes, including individuals with type 1 diabetes and gestational diabetes
- Women referred for diabetes care during pregnancy, or while breastfeeding or who intend to become pregnant during involvement in this trial
- Currently using real time CGM or FGM system
- Concurrent involvement in another clinical trial using diabetes pharmacotherapy
- Individuals with active malignancy undergoing treatment with chemotherapy and/or high dose glucocorticoids
- Individuals with rheumatic disease undergoing treatment with high dose glucocorticoids
- Planned magnetic resonance imaging (MRI), computed tomography (CT) scan, or high-frequency electrical heat (diathermy) treatment during the time of Libre wear
- Any cognitive or other disorders, in the investigator's opinion, that may interfere with participation or ability to follow the study protocol
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description In-person visit arm Standard of care In this arm, patients meeting eligibility criteria and consented into the study are randomized to an in-person visit with an Endocrinologist. This is currently the standard of care for patients referred for diabetes specialty care. Care by the Endocrinologist is provided as would typically be done, taking into account patient factors and preferences. Surveys will be administered to measure patient burden and self efficacy. Freestyle Libre sensor arm eConsult In this arm, patients meeting eligibility criteria and consented into the study are randomized to have the Freestyle Libre Pro continuous glucose monitor (CGM) placed at their primary care clinic. The data collected from the diagnostic CGM will be utilized in conjunction with diet, exercise and medication logs provided by the patient and information from the patient's electronic medical record to complete an eConsult with treatment recommendations. Implementation of these recommendations will be per the primary care provider's discretion in conjunction with conversation with the patient in follow up visits. Surveys will be administered to measure patient burden and self efficacy.
- Primary Outcome Measures
Name Time Method Hemoglobin A1c (A1c) at baseline baseline A1c will be obtained as standard of care and values documented in the medical record.
Percentage change in A1c to 12 months baseline, 12 months The percent change in A1c will be calculated from baseline to 12 months
Proportion of patients with A1c <8% 6 months, 12 months The proportion of participants with A1c \<8% (ADA target) will be calculated.
Glycemic control based on A1c 12 months A1c reduction of \> 1% with 20% non-inferiority margin
Hemoglobin A1c (A1c) at 6 months 6 months A1c will be obtained as standard of care and values documented in the medical record.
Hemoglobin A1c (A1c) at 12 months 12 months A1c will be obtained as standard of care and values documented in the medical record.
Hemoglobin A1c (A1c) at 3 months 3 months A1c will be obtained as standard of care and values documented in the medical record.
Percentage change in A1c to 6 months baseline, 6 months The percent change in A1c will be calculated from baseline to six months
Proportion of patients with A1c <7% 6 months, 12 months The proportion of participants with A1c \<7% (ADA target) will be calculated.
- Secondary Outcome Measures
Name Time Method Efficacy of embedded clinical pharmacists baseline, 3, 6, and 12 months Changes in hemoglobin A1c will be used to assess the efficacy of the embedded clinical pharmacists
Provider assessment of acceptability at baseline, 6 months, and completion of study period Results from a 16 item post intervention questionnaire developed by the investigators will be used to assess provider acceptability. It includes 10 questions with a 5 item Likert scale from 1= Strongly disagree to 5= Strongly agree that asks about the usefulness, feasibility and how much they liked the eConsult and the physician visits. There are also 2 open-ended questions soliciting qualitative information about the intervention.
Number of clinical visits for diabetes care 12 months The number of clinical visits (outpatient, inpatient and emergency department) for diabetes care will be calculated for each participant
Patient assessment of care burden within 2 weeks of the physician visit or eConsult Modified assessment of perceived research burden
Patient self efficacy and disease burden based on diabetes self management questionnaire and problem areas in diabetes short five-item short form questionnaire at baseline and 6 months Patient disease burden will be measured by the validated Problem Areas in Diabetes-5 question (PAID-5) survey. The five questions are from the original 20 item PAID survey (specifically questions 3, 6, 12, 16, and 19) and each has a 5-point Likert scale ranging from "not a problem" (score of 0) to "serious problem" (score of 4). The possible total scores of the PAID-5 ranges from 0 to 20, with higher scores implying greater emotional distress.
Cost effectiveness analysis (CEA) 12 months A Cost-Effectiveness Analysis will be done to compare the costs and health gains for the eConsult and standard of care interventions.
Trial Locations
- Locations (1)
Boston Medical Center
🇺🇸Boston, Massachusetts, United States