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OpenTrials
Completed

NCT Number: NCT07556783

Increasing the Use of Self Measured Home Blood Pressure Logs in the Management of Hypertension

The Telephone-Based Patient Outreach to Improve Home Blood Pressure Monitoring (HBPM) in Chronic Hypertension study is a pragmatic, randomized, open-label quality improvement implementation trial designed to evaluate the effectiveness of a structured telephone outreach intervention in increasing the proportion of patients with chronic hypertension who present to clinic visits with a completed home blood pressure log compared to the receipt of usual primary care services over a 90-day period. The study aims to address the inconsistent integration of HBPM-an evidence-based strategy endorsed by major guidelines to improve diagnostic accuracy and longitudinal management-into routine primary care workflows where no standardized educational or documentation process currently exists. Patients with documented chronic uncontrolled hypertension, defined as three documented readings exceeding 130/80 mmHg, are eligible for participation. Typically, patients at this academic primary care practice lack a standardized process for receiving education on home monitoring or a dedicated mechanism for documenting logs, which can lead to therapeutic inertia and missed opportunities to optimize treatment. The intervention is designed around a structured telephone outreach program led by medical students using a standardized script to provide direct patient education on the clinical value of HBPM and to encourage the completion and presentation of BP logs during subsequent primary care visits.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

AdventHealth Winter Park

Orlando, Florida, 32792, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients must have a documented diagnosis of chronic uncontrolled hypertension
  • "Uncontrolled" was defined as having three documented blood pressure readings exceeding 130/80 mmHg within the electronic health record.

Exclusion criteria

  • None

Treatment and study plan

A structured, telephone-based educational outreach to encourage HBPM

Other

Telephone-based educational outreach to encourage HBPM

Primary outcomes

  1. HBPM Log Adherence

    Time frame: Adherence was measured at follow-up within a 90-day window of the intervention.

    The primary outcome was the proportion of patients with a documented home blood pressure log in the electronic health record (EHR). A "documented log" was operationally defined as any notation in the medical record indicating that a patient presented with, reported, or submitted home blood pressure readings, whether through a scanned paper log, free-text documentation in a clinical note, or an entry in a structured data field

Secondary outcomes

  1. Change in Blood Pressure

    Time frame: The most recent follow-up measurement recorded within a 90-day window of the intervention.

    The secondary outcomes consisted of the mean change in both systolic and diastolic blood pressure. These clinical metrics were selected to evaluate the impact of the HBPM intervention on objective blood pressure control

Sponsors and collaborators

Lead sponsor

AdventHealth

Other

Registry information

Official study title

Telephone-Based Patient Outreach to Improve Self-Measured Blood Pressure Log Utilization in Chronic Hypertension: A Pragmatic Quality Improvement Randomized Implementation Trial

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Apr 29, 2026
Registry last updated
Apr 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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