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N/A N=4 Randomized Prevention

A Task Analysis Study of DECIDE For African American Patients With Type 2 Diabetes

Diabetes Mellitus, Type 2

Enrolled (actual)
4
Serious AEs
0.0%
Results posted
Mar 2026
Primary outcome: Primary: Percentage of Glycated Hemoglobin Among Participants at Baseline and 18-week Follow-up — 8.0; 7.40; 8.40; 7.35 Percentage of glycated hemoglobin — p=0.900

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
eDECIDE Web-based Intervention Group (Behavioral)
Age
Pediatric, Adult, Older Adult · 16+ yrs
Sex
All
Sponsor
University of Kansas Medical Center
Primary completion
Oct 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Glycated Hemoglobin Among Participants at Baseline and 18-week Follow-up
8.0; 7.40; 8.40; 7.35 0.900
SECONDARY
Health Problem Solving Scores Outcomes
22.54; 17.9; 22.96; 24.02 .6734
SECONDARY
Diabetes Self -Care Behaviors-monitoring Blood Glucose Levels
7; 6; 5; 3

Summary

The Decision-Making Education for Choices in Diabetes Every Day (DECIDE) program (copyrighted) was created by Dr. Felicia Hill-Briggs and is used by permission for the purpose of this pilot study. This problem-solving curriculum is used to help manage everyday problems when living with diabetes. The purpose of this project is to complete an in-depth review of the Decision-Making Education for Choices in Diabetes Every Day (DECIDE) curriculum, which is delivered in a group face-to-face setting. Using a task analysis process, the investigators will use the findings from the review to develop a web-site version that will be called eDECIDE for use with a community group in Kansas. Phase 3: will be a pilot clinical trial (2 Arm Study) which examines the use of the eDECIDE curriculum compared to the traditional DECIDE curriculum delivered to participants individually.

Eligibility Criteria

Inclusion Criteria

  • African American
  • English speaking
  • Access to the Internet daily
  • Reading level of at least 5th grade
  • Diagnosis of Type 2 Diabetes per one of the following
  • Fasting blood glucose ≥ to 126 mg/dL
  • 2 hr plasma glucose ≥ 200 mg/dL
  • Glycosylated hemoglobin HbA1c ≥ to 6.5%
  • Random plasma glucose ≥ 200 mg/dL

Exclusion Criteria

  • Glycosylated hemoglobin HbA1c ≤ 7.0
  • Pregnancy
  • Severe visual or hearing impairment or any existing condition that would limit or hinder one's ability to use the Internet
  • Dementia
  • Use of supplemental oxygen
  • Chest pain or angina
  • Prior lower extremity amputation
  • A diagnosis of a life threatening malignancy within the past year
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03855449). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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