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NCT04049500 Clinical Trial

Adapt and Incorporate dDPP Into Clinical Workflows

Nurse-Patient Relations Clinical Trial

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

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT04049500
Other study ID # 19-00758
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date September 2021
Est. completion date September 2026

Study information
Verified date October 2021
Source NYU Langone Health
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

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.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date September 2026
Est. primary completion date September 2026
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 100 Years
Eligibility 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.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Digital Diabetes Prevention Program (dDPP)
dDPP tool suite to integrate with the EHR and clinical workflows

Locations
Country Name City State
n/a

Sponsors (2)
Lead Sponsor Collaborator
NYU Langone Health National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Outcome
Type Measure Description Time frame Safety issue
Primary Usability will be assessed using a 5-point Likert scale 5 point likert scale is measured on a 5 point scale, 1 being "very unsatisfied" and 5 being "very satisfied." Higher scores mean more usability 12 Months
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