- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04591015
Dulce Digital-COVID Aware (DD-CA) Discharge Texting Platform for US/Mexico Border Hispanics With Diabetes + COVID-19
August 30, 2023 updated by: Athena Philis-Tsimikas, Scripps Whittier Diabetes Institute
The COVID-19 pandemic has triggered extremely high hospitalization rates where mitigation strategies are urgently necessary to aid vulnerable Hispanic and Latino populations who are experiencing health disparities as well as high type 2 diabetes (T2D) prevalence with poor clinical outcomes when compared to non-Hispanic populations.
The supplemental Dulce Digital-COVID Aware (DD-CA) intervention addresses specific barriers in diverse underserved Hispanic and Latino communities to improve glucose control and lower transmission of COVID-19 during a highly vulnerable period post hospitalization discharge, to reduce hospital readmission rates.
This supplement will integrate COVID educational messaging with glucose management messaging within a low-cost, easily adoptable digital texting platform and offer critical information in a culturally and linguistically relevant manner to address specific barriers in diverse underserved communities.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Hispanics, a group that shows higher type 2 diabetes (T2D) prevalence, and poor self-management and clinical outcomes, have been disproportionally adversely impacted by COVID-19.
The California Department of Public Health reports that Hispanics make up 39% of California's population but an unprecedented 57% of the confirmed COVID-19 cases.
This devastating finding is especially notable on the US/Mexico border.
Diabetes has emerged as a leading risk factor for severe COVID-19 illness leading to hospitalization, is associated with greater disease severity and mortality and is an independent predictor of intensive care placement and invasive ventilation.
It is becoming increasingly clear that maintaining good glucose control improves prognosis of COVID-19 among people with pre-existing T2D.
However, social distancing, quarantine, and stay-at-home/lockdown guidelines may impact one's ability to maintain adequate glycemic control.
Research is needed to evaluate the effect and clinical outcomes of a flexible, easily adopted low cost digital intervention that improves glucose excursions and provides urgently needed COVID-19 mitigation strategies, among rapidly rising groups of high-risk Hispanics with poorly controlled T2D in US/Mexico border communities.
Strong evidence from our parent grant Dulce Digital-Me (DD-ME), supports the use of technology (such as text messaging) alone or in combination with coaching interventions as a viable and desired method of delivering tailored diabetes self-management education and COVID awareness messaging to high-risk, underserved populations in a manner that is more convenient for both patients and staff while having the added benefit of being cost-effective for health systems, especially within low resource settings.
However, effective interventions may encounter barriers which preclude guaranteed success upon implementation in the real world.
This project, taking place along the San Diego/Tijuana border, historically the busiest land port of entry in the Western Hemisphere, will assess the effect of providing an enhanced digital texting intervention-Dulce Digital-COVID Aware (DD-CA) to N = 172 Hispanic patients with T2D upon discharge from a recent hospitalization.
Key outcomes will assess the impact of DD-CA on hospital readmissions at 30, 90 and 180 days post-discharge, glucose control and patient reported outcomes at 90 and 180 days post-discharge while also assessing COVID status and the implementation process.
Given that DD-CA offers the potential to address many of the practical barriers to access and extend the reach of diabetes services, while additionally providing COVID awareness support, it offers an ideal low-cost and flexible solution to reduce hospital admissions and re-admissions in US/Mexico border communities significantly and simultaneously affected by COVID-19 and T2D.
Implemented in a typical hospital and post-discharge setting, it augments existing care team processes, thus providing a valuable test of real-world effectiveness.
More importantly, by helping to reduce existing inequities in access to diabetes and COVID-19 care, this program aims to improve health outcomes on a larger scale.
Study Type
Interventional
Enrollment (Actual)
172
Phase
- Phase 3
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
Chula Vista, California, United States, 91910
- Scripps Mercy Hospital Chula Vista
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Are a patient admitted to a Scripps Mercy Hospital,
- Consider yourself Hispanic/Latino, of any race
- Are 18 years of age or older,
- Speak English or Spanish,
- Have type 2 diabetes and A1c ≥ 7% in the last 90 days, and
- Have a cellphone that can receive/send text messages.
Exclusion Criteria:
- Are pregnant,
- Are currently participating in another diabetes or COVID-19 related study, or
- Do not meet all eligibility inclusion criteria.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: DD-CA
In the DD-CA arm, participants will be offered a proven digital texting platform in their language of preference (Spanish/English) as part of the diabetes transitions discharge program with added COVID support messages.
|
In the DD-CA group, participants will be offered a proven digital texting platform in their language of preference (Spanish/English) as part of the diabetes transitions discharge program with educational, motivational and medication adherence messaging that is currently an arm of our parent DD-ME grant with added COVID support messages that provide information addressing identified barriers in Hispanic underserved communities (e.g.
obtaining testing supplies and medications, accessing routine medical care, and completing other important diabetes self-management behaviors such as healthful eating, exercise, social distancing, quarantine, and stay-at-home/lockdown guidelines).
|
Active Comparator: Usual Care (UC)
UC participants will not receive the added COVID support messages, both arms will have a referral placed to the Diabetes Transitions Service (DTS) as part of usual care at the time of discharge.
|
In the UC group, participants will not receive the added COVID support messages, both groups will have a referral placed to the Diabetes Transitions Service (DTS) at the time of discharge as part of usual care.
Participants will be contacted by a peer health coach following protocol to coordinate care with outpatient health and other community resources.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hospital Readmission Rate Within 30 Days of Discharge
Time Frame: Within 30 days of discharge
|
Number of Participants With at Least 1 Hospital Readmission Within 30 Days After Enrollment, analyzed for full study sample
|
Within 30 days of discharge
|
Glycosylated Hemoglobin (HbA1c) - Change From Baseline to 90 Days
Time Frame: 90 days from baseline
|
Change in Glycosylated Hemoglobin (HbA1c) 90 days from baseline.
A negative mean indicates positive change in HbA1c.
|
90 days from baseline
|
Glycosylated Hemoglobin (HbA1c) - Change From Baseline to 180 Days
Time Frame: 180 days from baseline
|
Change in Glycosylated Hemoglobin (HbA1c) 180 days from baseline.
A negative mean indicates positive change in HbA1c.
|
180 days from baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hospital Readmission Rate Within 90 Days of Discharge
Time Frame: Within 90 days of discharge
|
Number of Participants With at Least 1 Hospital Readmission Within 90 Days After Enrollment, analyzed for full study sample.
|
Within 90 days of discharge
|
Diabetes Distress Scale - Change From Baseline to 90 Days
Time Frame: 90 days from baseline
|
Diabetes distress as reported by patient; 90 days from baseline.
The minimum score is 1 and maximum score is 6 with a higher score representing worse outcome or greater diabetes related emotional stress.
A negative mean indicates a positive change in the diabetes distress score.
|
90 days from baseline
|
Diabetes Distress Scale - Change From Baseline to 180 Days
Time Frame: 180 days from baseline
|
Diabetes distress as reported by patient; 180 days from baseline.
The minimum score is 1 and maximum score is 6 with a higher score representing worse outcome or greater diabetes-related emotional stress.
A negative mean indicates a positive change in the diabetes distress score.
|
180 days from baseline
|
Summary of Diabetes Self-Care Activities - Diet - Change From Baseline to 90 Days
Time Frame: 90 days from baseline
|
Diabetes self-care activities related to Diet as reported by patient; 90 days from baseline; The minimum score is 0 and maximum score is 7 with a higher score representing better adherence to diabetes diet self-management behaviors.
A positive mean indicates a positive change in the diet self-care activities.
|
90 days from baseline
|
Summary of Diabetes Self-Care Activities - Exercise - Change From Baseline to 90 Days
Time Frame: 90 days from baseline
|
Diabetes self-care activities related to Exercise as reported by patient; 90 days from baseline; The minimum score is 0 and maximum score is 7 with a higher score representing better adherence to diabetes exercise self-management behaviors.
A positive mean indicates a positive change in exercise self-care activities.
|
90 days from baseline
|
Summary of Diabetes Self-Care Activities - Blood Sugar - Change From Baseline to 90 Days
Time Frame: 90 days from baseline
|
Diabetes self-care activities related to Blood Sugar as reported by patient; 90 days from baseline; The minimum score is 0 and maximum score is 7 with a higher score representing better adherence to diabetes blood sugar self-management behaviors.
A positive mean indicates a positive change in blood sugar self-care activities.
|
90 days from baseline
|
Summary of Diabetes Self-Care Activities - Diet - Change From Baseline to 180 Days
Time Frame: 180 days from baseline
|
Diabetes self-care activities related to Diet as reported by patient; 180 days from baseline; The minimum score is 0 and maximum score is 7 with a higher score representing better adherence to diabetes diet self-management behaviors.
A positive mean indicates a positive change in diet self-care activities.
|
180 days from baseline
|
Summary of Diabetes Self-Care Activities - Exercise - Change From Baseline to 180 Days
Time Frame: 180 days from baseline
|
Diabetes self-care activities related to Exercise as reported by patient; 180 days from baseline; The minimum score is 0 and maximum score is 7 with a higher score representing better adherence to diabetes exercise self-management behaviors.
A positive mean indicates a positive change in exercise self-care activities.
|
180 days from baseline
|
Summary of Diabetes Self-Care Activities - Blood Sugar - Change From Baseline to 180 Days
Time Frame: 180 days from baseline
|
Diabetes self-care activities related to Blood Sugar as reported by patient; 180 days from baseline; The minimum score is 0 and maximum score is 7 with a higher score representing better adherence to diabetes blood sugar self-management behaviors.
A positive mean indicates a positive change in blood sugar self-care activities.
|
180 days from baseline
|
COVID-19 Patient Survey (Phenix Toolkit) Within 90 Days of Discharge
Time Frame: Within 90 days of discharge
|
COVID-19 Patient Survey was used to assess COVID-19 diagnosis status and determine whether new infections occurred in the 90-day post-discharge time frame.
|
Within 90 days of discharge
|
COVID-19 Patient Survey (Phenix Toolkit) Within 180 Days of Discharge
Time Frame: Within 180 days of discharge
|
COVID-19 Patient Survey was used to assess COVID-19 diagnosis status and determine whether new infections occurred in the 180-day post-discharge time frame.
|
Within 180 days of discharge
|
Patient-Reported Outcomes Measurement Information System (PROMIS) Global-10 Health Scale - Physical - Change Between Baseline and 90 Days
Time Frame: 90 days from baseline
|
Patient-Reported Outcomes Measurement Information System (PROMIS) Global-10 Health Scale was a measure of overall score patient-reported physical health collected at baseline and 90 days.
The minimum score on this scale is 0 and maximum score is 100.
A higher score indicates a better outcome/higher quality of life.
When the means are calculated between baseline and 90 days, a positive mean indicates a better outcome/higher quality of life.
|
90 days from baseline
|
Patient-Reported Outcomes Measurement Information System (PROMIS) Global-10 Health Scale - Mental - Change Between Baseline and 90 Days
Time Frame: 90 days from baseline
|
Patient-Reported Outcomes Measurement Information System (PROMIS) Global-10 Health Scale was a measure of overall score patient-reported mental health 90 days from baseline.
The minimum score on this scale is 0 and maximum score is 100.
A higher score indicates a better outcome/higher quality of life.
When the means are calculated between baseline and 90 days, a positive mean indicates a better outcome/higher quality of life and a negative mean indicates a worse outcome/lower quality of life.
|
90 days from baseline
|
Patient-Reported Outcomes Measurement Information System (PROMIS) Global-10 Health Scale - Physical - Change Between Baseline and 180 Days
Time Frame: 180 days from baseline
|
Patient-Reported Outcomes Measurement Information System (PROMIS) Global-10 Health Scale was a measure of overall score patient-reported physical health 180 days from baseline.
The minimum score on this scale is 0 and maximum score is 100.
A higher score indicates a better outcome/higher quality of life.
When the means are calculated between baseline and 180 days, a positive mean indicates a better outcome/higher quality of life.
|
180 days from baseline
|
Patient-Reported Outcomes Measurement Information System (PROMIS) Global-10 Health Scale - Mental - Change Between Baseline and 180 Days
Time Frame: 180 days from baseline
|
Patient-Reported Outcomes Measurement Information System (PROMIS) Global-10 Health Scale was a measure of overall score patient-reported mental health 180 days from baseline.
The minimum score on this scale is 0 and maximum score is 100.
A higher score indicates a better outcome/higher quality of life.
When the means are calculated between baseline and 180 days, a positive mean indicates a better outcome/higher quality of life, and a negative mean indicates a worse outcome/lower quality of life.
|
180 days from baseline
|
Knowledge, Attitudes and Practice Toward COVID-19 Survey - Change From Baseline to 90 Days
Time Frame: 90 days from baseline
|
Knowledge, Attitudes and Practice Toward COVID-19 Survey was used to measure knowledge and attitudes related to COVID-19 at 90 days from baseline.
The minimum score on this scale is 0 and maximum score is 12, with higher scores indicating greater knowledge of COVID-19.
A negative mean indicates lesser knowledge of COVID-19.
|
90 days from baseline
|
Knowledge, Attitudes and Practice Toward COVID-19 Survey - Change From Baseline to 180 Days
Time Frame: 180 days from baseline
|
Knowledge, Attitudes and Practice Toward COVID-19 Survey was used to measure knowledge and attitudes related to COVID-19 at 180 days from baseline.
The minimum score on this scale is 0 and maximum score is 12, with higher scores indicating greater knowledge of COVID-19.
A negative mean indicates lesser knowledge of COVID-19.
|
180 days from baseline
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Readmission Rate
Time Frame: 90-days, 180-days
|
Exploratory analyses will be conducted similarly to our Primary Outcome.
The EMR will be used to identify readmissions during each patient's unique follow up period.
Unadjusted between group differences will first be analyzed by comparing proportion of patients with any hospital readmissions within the 90-day period by a Fisher's exact t-test.
Followup analyses will be conducted using multiple logistic regression models to account for gender, ethnicity, race, comorbid conditions including COVID-19, medication use, and baseline glycemic control, in addition to study arm, as fixed effects in predicting the exploratory outcome, rate of readmissions within 90 and 180-days.
|
90-days, 180-days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Athena Philis-Tsimikas, MD, Scripps Whittier Diabetes Institute
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 1, 2021
Primary Completion (Actual)
August 31, 2022
Study Completion (Actual)
August 31, 2022
Study Registration Dates
First Submitted
October 5, 2020
First Submitted That Met QC Criteria
October 15, 2020
First Posted (Actual)
October 19, 2020
Study Record Updates
Last Update Posted (Actual)
September 28, 2023
Last Update Submitted That Met QC Criteria
August 30, 2023
Last Verified
August 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Glucose Metabolism Disorders
- Metabolic Diseases
- Coronavirus Infections
- Coronaviridae Infections
- Nidovirales Infections
- RNA Virus Infections
- Virus Diseases
- Infections
- Respiratory Tract Infections
- Respiratory Tract Diseases
- Pneumonia, Viral
- Pneumonia
- Lung Diseases
- Endocrine System Diseases
- COVID-19
- Diabetes Mellitus
- Diabetes Mellitus, Type 2
Other Study ID Numbers
- 3R01DK112322-05S1 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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