Increasing Uptake of EHR-enabled Population Health Outreach Strategies to Improve Diabetes Screening
Enrolling by invitation · Not applicable
Conditions studied: Diabetes Mellitus, Type 2, Pre Diabetes
In brief
The study team's central hypothesis is that the Parkland Diabetes Detection Program (PDDP) screening invitations targeted by race/ethnicity with culturally concordant messaging and tailored by glycemic risk (known PDM vs. unknown glycemic state) plus phone-based navigation of non-responders will be more effective at closing screening gaps than PDDP generic screening invitations and usual care, opportunistic screening alone.
Key facts
- Study ID
- NCT05730582
- Run by
- University of Texas Southwestern Medical Center
- People needed
- 500000
- Starts
- 2024-03-05
- Expected to finish
- 2028-12-30
- Last updated by the study team
- 2026-05-08
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patient is alive at time of data extraction
- Age >= 18 at time of data extraction and <76
- Visit with PCP at Parkland clinic in the last 18 months (548 days), where Encounter type = Virtual Visit or Encounter type = Office Visit
- Patient NOT included in Parkland Diabetes Registry
- Preferred language is Spanish or English
- Ethnicity is Hispanic or Non-Hispanic
- Race is White or Black
- Patient is not pregnant in last 12 months
- Exclusion Criteria for Study Population 1: Prediabetes Glycemic Risk Group
- Last A1C value <5.7 (normal)
- Last A1C value >6.4 (diabetes)
- Last A1C value = blank (unchecked)
- Last A1C date occurred within last 12 months from date of export
- Exclusion Criteria for Study Population 2: Score-Based Glycemic Risk Group
- Risk score <9
- Last A1C date occurred in last 30 months from date of export
- Last A1C value was >5.7 (PDM/DM)
Where it is running
- Parkland Health — Dallas, Texas, United States
Full record on ClinicalTrials.gov
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