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NCT05126082Completed

Pediatric Blood Pressure Clinical Decision Support Tool (PedsBP CDS)

Improving Recognition and Management of Hypertension in Youth: Comparing Approaches for Extending Effective CDS for Use in a Large Rural Health System

Source: ClinicalTrials.gov · Last updated 22 Jan 2026

Brief summary (registry, in English)

The goal of the PedsBP CDS research project is to adapt a previously tested web-based clinical decision support tool that appropriately identifies high blood pressure in youth for use in a primarily rural health system and compare approaches to CDS implementation in 45 primary care clinics treating children in 3 upper Midwest states. This project will advance implementation science and address a critical need for youth at risk for cardiovascular disease and with limited access to pediatric subspecialty care.

Status (registry)
Completed
Study type
Interventional
Enrollment
41054 (actual)
First submitted
7 Oct 2021
Start date
1 Aug 2022
Primary completion date
31 Jan 2025
Lead sponsor
HealthPartners Institute
NCT number
NCT05126082

What you commit to

  • Study type: Interventional
  • Participants enrolled: 41054
  • From 1 Aug 2022 to the primary completion date, 31 Jan 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • known HT diagnosis or taking antihypertensive medication at index visit
  • opted out of use of their data for research via general consent prior to performing analyses

Age

  • outside of the inclusion age range (\<6 years and ≥18 years) at index visit

Other

  • Patients will be excluded from analyses if the following criteria are met:
  • pregnant or postpartum adolescents during study period

Who the study is looking for

  • Patients will be eligible for the PedsBP CDS if
  • 6-17 years of age
  • BP measured and entered in the vital sign section during an ambulatory primary care visit in a randomized primary care clinic
  • not pregnant or postpartum
    • Patients must meet these eligibility criteria to be included into study analyses:
  • have at least one index visit with a primary care provider at a randomized clinic in the intervention period
  • meet eligibility for PedsBP CDS at index visit (a-c above)
  • no previous HT diagnosis prior to index visit
  • not taking antihypertensive medication prior to index visit
  • not opted out of use of their data for research via general consent prior to performing analyses
    • Primary care providers must meet these eligibility criteria to participate in this study:
  • practice at a randomized primary care clinic
  • be a pediatric or family medicine care provider (pediatrician, family physician, nurse practitioner or physician assistant), and
  • provide ongoing clinical care for children and adolescents

Age in the registry: 6 years to 17 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Essentia Health
Coordinator of this site? Confirm its status
DuluthUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.