Skip to content

Adapt and Incorporate dDPP Into Clinical Workflows

An Observational Study to Adapt a Digital Diabetes Prevention Program (dDPP) and Incorporate it Into the Clinical Workflows.

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04049500
Enrollment
0
Registered
2019-08-08
Start date
2021-09-30
Completion date
2026-09-30
Last updated
2021-10-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nurse-Patient Relations, Physician-Patient Relations

Keywords

Physicians, Nurses, Practice assistants, Health coaches, Population health managers, Patient navigators

Brief summary

This observational study will seek to adapt a digital diabetes prevention program (dDPP) tool suite into clinical workflows. This tool pushes key dDPP data elements (e.g. weight and daily step count) directly into EHR workflows of primary care to enhance patient engagement. It seeks to determine the impact of combining adapted visualizations and summaries of key dDPP data elements directly into the EHR with automated notifications and messaging designed to enhance patient engagement in the dDPP. The study will involve provider workflow analysis based on observation and facilitated group tool adaptation sessions.

Detailed description

Primary objective: to examine the impact of the dDPP tool suite on the EHR and clinical workflows, and identify optimization opportunities. Secondary objective: to assess the usability of the proposed dDPP tool suite in clinical practice.

Interventions

dDPP tool suite to integrate with the EHR and clinical workflows

Sponsors

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
NYU Langone Health
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

* Physicians * Nurses * Practice assistants * Health coaches * Population health managers * Patient navigators

Exclusion criteria

* Practices will be ineligible for participation if they treat fewer than 100 adults with prediabetes.

Design outcomes

Primary

MeasureTime frameDescription
Usability will be assessed using a 5-point Likert scale12 Months5 point likert scale is measured on a 5 point scale, 1 being very unsatisfied and 5 being very satisfied. Higher scores mean more usability

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026