← Back to Search

Digital Diabetes Self-Management for Diabetes (Dulce Digital Trial)

N/A
Recruiting
Led By Athena Philis-Tsimikas, MD
Research Sponsored by Scripps Whittier Diabetes Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Diagnosis of Type 2 Diabetes
Be older than 18 years old
Must not have
Not willing to carry a mobile phone
Severe illness precluding visits to clinic
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
No Placebo-Only Group

Summary

This trial is testing three ways to help underserved adults with diabetes manage their condition: in-person classes, online group sessions, and text messages. The goal is to see which method works best for people who often face challenges like low income and limited access to healthcare. By teaching them how to manage their diabetes, the study aims to help them make healthier choices and control their blood sugar levels better.

Who is the study for?
This trial is for Hispanic/Latino adults with Type 2 Diabetes, registered at Scripps Health, and an HbA1c level ≥8% in the last 60 days. It's not for those with recent substance abuse issues, severe health problems like anemia or liver dysfunction, minimal literacy, or who don't speak Spanish/English.
What is being tested?
Dulce Digital 2.0 evaluates two digital adaptations of Project Dulce aimed at improving diabetes self-management via text messages and telehealth platforms compared to traditional in-person education.
What are the potential side effects?
Since this trial involves educational interventions rather than medications, typical drug side effects are not expected. However, participants may experience discomfort from increased engagement with technology.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I have been diagnosed with Type 2 Diabetes.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
Select...
I am not willing to carry a mobile phone.
Select...
I am too ill to visit the clinic for treatments.
Select...
My primary language is not English or Spanish.
Select...
I have severe hearing or vision problems.
Select...
I have anemia.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 6 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change from Baseline in Baseline Glycosylated Hemoglobin A1C (HbA1c) at 3 months
Change from Baseline in Baseline Glycosylated Hemoglobin A1C (HbA1c) at 6 months
Secondary study objectives
Change from Baseline Diabetes Distress (DDS-17) at 3 months
Change from Baseline Diabetes Distress (DDS-17) at 6 months
Change from Baseline Diabetes Treatment Satisfaction Questionnaire (DTSQ) at 3 months
+1 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

3Treatment groups
Experimental Treatment
Group I: Project Dulce Telehealth DSME/SExperimental Treatment1 Intervention
Patients will participate in live a peer-led Telehealth diabetes self-management education and support program.
Group II: Project Dulce Live DSME/SExperimental Treatment1 Intervention
Patients will participate in live a peer-led Telehealth diabetes self-management education and support program.
Group III: Dulce DigitalExperimental Treatment1 Intervention
Patients will participate in a text-based diabetes self-management educational and support (DSME/S) program and receive ongoing support via text messages designed to improve knowledge, health beliefs, self-management behaviors and clinical outcomes.

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for diabetes, particularly those involving telehealth and digital health literacy, focus on improving patients' ability to manage their condition through education and remote monitoring. These interventions often include live self-management education via telehealth platforms and text-based messages that encourage healthy behaviors. The primary mechanism of action is enhancing patients' knowledge and skills to manage their blood glucose levels, adhere to medication regimens, and make informed lifestyle choices. This approach is crucial for diabetes patients as it empowers them to take control of their health, potentially leading to better glycemic control and reduced complications.
E-health education interventions on HbA<sub>1c</sub> in patients with type 1 diabetes on intensive insulin therapy: A systematic review and meta-analysis of randomized controlled trials.Effectiveness of Telemedicine Solutions for the Management of Patients With Diabetes: Protocol for a Systematic Review and Meta-Analysis.Effectiveness of technology-assisted case management in low income adults with type 2 diabetes (TACM-DM): study protocol for a randomized controlled trial.

Find a Location

Who is running the clinical trial?

Scripps Whittier Diabetes InstituteLead Sponsor
18 Previous Clinical Trials
5,299 Total Patients Enrolled
3 Trials studying Diabetes
1,422 Patients Enrolled for Diabetes
Athena Philis-Tsimikas, MDPrincipal InvestigatorScripps Health
14 Previous Clinical Trials
4,569 Total Patients Enrolled
3 Trials studying Diabetes
1,422 Patients Enrolled for Diabetes

Media Library

Dulce Digital Text-Based Education Clinical Trial Eligibility Overview. Trial Name: NCT05416060 — N/A
Diabetes Research Study Groups: Dulce Digital, Project Dulce Telehealth DSME/S, Project Dulce Live DSME/S
Diabetes Clinical Trial 2023: Dulce Digital Text-Based Education Highlights & Side Effects. Trial Name: NCT05416060 — N/A
Dulce Digital Text-Based Education 2023 Treatment Timeline for Medical Study. Trial Name: NCT05416060 — N/A
~0 spots leftby Nov 2024