Clinical Trials Directory

Trials / Completed

CompletedNCT02957721

Diabetes Engagement and Activation Platform

DEAP: Diabetes Engagement and Activation Platform

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
350 (actual)
Sponsor
Virginia Commonwealth University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The following are hypothesized: 1. The Diabetes Engagement and Activation Platform (DEAP) can be integrated into primary care workflow to facilitate the care of patients with type 2 diabetes. 2. The DEAP intervention will be feasible and acceptable to patients with type 2 diabetes. 3. The DEAP intervention will enhance patient activation and improve type 2 diabetes self management and glucose control

Detailed description

Aim 1: To evaluate how primary care practices adopt and integrate DEAP into routine workflow including identification of barriers and facilitators to support acceptable, feasible, and sustainable use of the system. * Sub-aim 1.1: Measure the proportion of clinicians and care team members who engage patients through the DEAP intervention as well as the types of patient support activities they address; assess the representativeness of participating clinicians and care team members in relation to all practice staff; and assess how they integrated DEAP into the care of type 2 diabetes patients. * Sub-aim 1.2: Assess how practices redesign workflow, overcome barriers, and enhance facilitators in order to integrate DEAP. * Sub-aim 1.3: Determine processes for sustaining DEAP beyond the project funding period . Aim 2: To compare, relative to usual care, the effectiveness of the DEAP intervention. * Sub Aim 2.1: Measure the proportion and representativeness of eligible patients who choose to enroll; access the DEAP curriculum; complete the DEAP curriculum; and contact care team members. . * Sub Aim 2.2: Compare the change in the average glycosylated hemoglobin (primary outcome), Body Mass Index, systolic blood pressure, and type 2 diabetes (T2D) medications and patient activation (secondary outcomes) from baseline to 3 months and from 3 to 6 months for patients randomized to DEAP versus usual care. Sub Aim 2.3: Assess the clarity, readability and acceptability of the DEAP curricula materials for T2D patients enrolled in the intervention.

Conditions

Interventions

TypeNameDescription
OTHERUsual CarePatients will not be given the intervention but receive usual care for T2D.

Timeline

Start date
2017-11-01
Primary completion
2018-11-05
Completion
2018-11-05
First posted
2016-11-08
Last updated
2018-11-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02957721. Inclusion in this directory is not an endorsement.