- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04835493
Evaluating Telementoring for CHW-centered Diabetes Initiatives
Evaluating Telementoring to Initiate a Multidimensional Diabetes Program for Latino(a)s in Community Clinics: A Randomized Clinical Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Diabetes is a major public health problem in Latino(a)s. There are escalating numbers of Latino(a)s diagnosed with diabetes and at disproportionate rates compared to other ethnicities. Numerous interventions have been initiated to improve minority healthcare including diabetes group visits, which have been valuable in improving education and glycemic control. In our group visit investigations, investigators initiated Community Health Workers (CHWs)-local community members who serve as culturally-sensitive patient liaisons to the healthcare system-as part of the multidisciplinary team. Investigators demonstrated that CHWs are vital team members and particularly helpful in identifying medication-access barriers. However, CHWs are frontline workers and often left unsupported and poorly supervised. Investigators used these data to pioneer the combination of four diabetes interventions. This trial showed that individuals randomized to the intervention significantly improved glycemic control, blood pressure and adherence to American Diabetes Association standards compared to usual care. The study also showed that telehealth (mobile health (mHealth) and ZOOM video conferencing) was instrumental in supporting CHWs in their work and enhancing their communication with patients.
The COVID-19 pandemic has highlighted the expansive use of telehealth and its ability to improve healthcare. It has also underscored the pressing need to improve care for low-income minorities. Though diabetes programs are valuable in improving education and clinical outcomes, they are often difficult to initiate in low-income settings. Pragmatic implementation using telehealth to mentor local clinic teams of providers and CHWs is promising to address these barriers. Investigators have pilot data showing the feasibility of telementoring a local clinic to initiate our program that has resulted in improved HbA1c levels but it needs to be tested within a larger sample. In the proposed study investigators will evaluate this approach in a randomized clinical trial (N=320; intervention=160) of low-income, adult Latino(a)s with type 2 diabetes randomized to the diabetes program intervention versus usual care (UC). Our research group will provide telementoring to local clinic teams to initiate our program into their clinics. To evaluate efficacy, investigators will compare the intervention versus UC clinical changes including HbA1c (primary outcome), blood pressure, cholesterol, and body mass index from baseline to 12-months (AIM 1). To compare longitudinal data of study arms, investigators will follow these clinical measures until 36 months (AIM 2). Investigators will also provide program acceptability and evaluation data for participants and clinic teams from baseline to 12-months (AIM 3). Investigators hypothesize that intervention participants will have superior and more sustainable clinical outcomes compared to UC individuals and that the intervention will have high levels of acceptability and evaluation data. Investigators anticipate that the proposed study will provide justification of telementoring to initiate the intervention and strong evidence to improve the longitudinal care of low-income Latino(a)s with diabetes.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Texas
-
Houston, Texas, United States, 77030
- University of Texas Medical Branch
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- self-identified Latino(a)
- Spanish-speaking
- >/=18 years
- type 2 diabetes (T2D), e.g., HbA1c >/=6.5%, provider documented T2D, on oral anti-hyperglycemic
- uninsured, <150% federal poverty level
Exclusion Criteria:
- no show to all group visits
- condition that may alter HbA1c levels, e.g., recent blood transfusion
- patients at high-risk or not appropriate for care in a group setting e.g., pregnancy, severe cognitive impairment, frequent clinic appointments for labile glucose/medication titration e.g., insulin.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
Intervention individuals will receive the 12-month diabetes program
|
In the proposed study, we will conduct a randomized clinical trial of low-income, adult Latino(a)s with type 2 diabetes randomized at the individual level a telehealth-supported, integrated CHWs, medication-access, diabetes education program) (intervention) versus usual care (UC).
Our research team will provide telementoring to local clinic teams (providers and CHWs) to initiate the 12-month the program into their clinics.
|
|
Other: Usual Care (UC)
We will define UC as usual clinical care, which consists of diabetes management provider encounters (mean quarterly) plus monthly individual appointments with a pharm-Ds or nutritionists as clinically indicated.
In addition, clinics offer multiple other individual and group opportunities.
|
In the proposed study, we will conduct a randomized clinical trial of low-income, adult Latino(a)s with type 2 diabetes randomized at the individual level a telehealth-supported, integrated CHWs, medication-access, diabetes education program) (intervention) versus usual care (UC).
Our research team will provide telementoring to local clinic teams (providers and CHWs) to initiate the 12-month the program into their clinics.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
HbA1c
Time Frame: Baseline to 12-months
|
Compare intervention versus control HbA1c levels
|
Baseline to 12-months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Community Health Worker (CHW) knowledge
Time Frame: 12-months
|
At 12-months; Knowledge as measured the CHW posttest, which includes 24-questions from the Star Education Study diabetes knowledge test, which has shown validity and reliability in English and Spanish and our TIME 25-question diabetes medication test that has been previously published.
Tests are multiple choice with 4 possible answers.
|
12-months
|
|
Telehealth Acceptability
Time Frame: 12-months
|
Acceptability as measured by the Telehealth Usability Questionnaire, a 21-question survey of telehealth acceptability.
Items are ranked on a 5-item scale (1 not acceptable, 5 very acceptable) and divided into six subsections that have shown good to excellent internal consistency.
|
12-months
|
|
Blood pressure
Time Frame: Baseline to 12-months
|
Compare intervention versus control blood pressure levels (systolic and diastolic)
|
Baseline to 12-months
|
|
Body Mass Index (BMI)
Time Frame: Baseline to 12-months
|
Compare intervention versus control BMI levels
|
Baseline to 12-months
|
|
Cholesterol
Time Frame: Baseline to 12-months
|
Compare intervention versus control cholesterol levels
|
Baseline to 12-months
|
|
American Diabetes Association (ADA) adherence measures: Diabetes foot exam
Time Frame: Baseline to 12-months
|
Compare intervention versus control adherence to diabetes foot exams
|
Baseline to 12-months
|
|
ADA adherence measures: B12 screening
Time Frame: Baseline to 12-months
|
Compare intervention versus control adherence to B12 screening
|
Baseline to 12-months
|
|
ADA adherence measures: Diabetes eye exam
Time Frame: Baseline to 12-months
|
Compare intervention versus control adherence to diabetes eye exams
|
Baseline to 12-months
|
|
ADA adherence measures: urine microalbumin screening
Time Frame: Baseline to 12-months
|
Compare intervention versus control adherence to urine microalbumin screening
|
Baseline to 12-months
|
|
ADA adherence measures: flu vaccination
Time Frame: Baseline to 12-months
|
Compare intervention versus control adherence to flu vaccination
|
Baseline to 12-months
|
|
ADA adherence measures: statin therapy
Time Frame: Baseline to 12-months
|
Compare intervention versus control adherence to statin therapy
|
Baseline to 12-months
|
|
Sustainable clinical outcomes: HbA1c
Time Frame: baseline to 36-months
|
Compared to control, the intervention will have more sustainable HbA1c levels
|
baseline to 36-months
|
|
Sustainable clinical outcomes: Blood pressure
Time Frame: baseline to 36-months
|
Compared to control, the intervention will have more sustainable blood pressure levels (systolic and diastolic)
|
baseline to 36-months
|
|
Sustainable clinical outcomes: BMI
Time Frame: baseline to 36-months
|
Compared to control, the intervention will have more sustainable BMI levels
|
baseline to 36-months
|
|
Program satisfaction
Time Frame: 12-months
|
Anticipate >/=80% patient satisfaction as demonstrated by our 12-question satisfaction survey questions (on Likert scales of 1 to 10 (n=5 questions) where 10 is very satisfied and 1 is not at all satisfied and from 1-4 (n=3 questions) where 4 is very satisfied and 1 is not satisfied).
There are three open-ended questions.
|
12-months
|
|
Attrition
Time Frame: baseline to 12-months
|
Rate of attrition for intervention participants
|
baseline to 12-months
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Elizabeth Vaughan, DO, UTMB
Publications and helpful links
General Publications
- Ameri M, Jabbar LA, Kim S, Raji M, Samson SL, Vaughan EM. Training clinicians to facilitate diabetes group visits. BMC Med Educ. 2025 Feb 25;25(1):309. doi: 10.1186/s12909-025-06876-7.
- Porterfield L, Warren V, Schick V, Gulliot-Wright S, Temple JR, Vaughan EM. Addressing Training Gaps: A Competency-Based, Telehealth Training Initiative for Community Health Workers. Telemed Rep. 2023 Jun 16;4(1):126-134. doi: 10.1089/tmr.2023.0007. eCollection 2023.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 22-0224
- R01DK129474 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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