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Clinical Trials/NCT07208669
NCT07208669RecruitingNot Applicable

Evaluating Whether Treating Elevated Blood Pressure in the Inpatient Setting Impacts Patient Outcomes: the ACT-BP Pilot

Elizabeth Pfoh2 sites in 1 country4 target enrollmentStarted: November 11, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
4
Locations
2
Primary Endpoint
Primary Outcome

Study Overview

Brief Summary

The vast majority of the 36.2 million individuals admitted to U.S. hospitals are diagnosed with hypertension and experience an elevated blood pressure (BP) reading during hospitalization. There are no guidelines for managing asymptomatically elevated BPs in the inpatient setting, and growing observational evidence suggests that antihypertensive medication intensification increases harm. The proposed study tests whether a unit-based intervention (ACT-BP) can reduce antihypertensive medication intensification and provides information that is scientifically necessary for designing a cluster-randomized clinical trial that identifies the impact of intensification after experiencing an asymptomatically elevated BP on patient outcomes.

Detailed Description

Approximately 50-72% of the 36.2 million individuals admitted to U.S. hospitals are diagnosed with hypertension. Hypertension increases the risk of devastating cardiovascular outcomes, such as strokes, heart attacks, and heart failure. Three-quarters of admitted patients experience at least one elevated blood pressure (BP) (>140/90) during hospitalization. While BP is usually elevated for benign reasons, including pain and anxiety, acutely elevated BP can cause end-organ damage. Currently, no guidelines exist for managing asymptomatically elevated BP in the inpatient setting. There is growing observational evidence that antihypertensive medication intensification for asymptomatically elevated BP can result in adverse outcomes, such as increased readmission. Since observational studies are biased, a large-scale clinical trial is needed to identify whether to treat asymptomatically elevated BPs in the hospital. Yet, it would be unethical and costly to randomize individual patients to receive antihypertensive medication intensification. To overcome these obstacles, this study uses hospital-unit-level intervention, ACT-BP. ACT-BP removes standing orders to call physicians about elevated BPs (which encourages treatment due to social desirability bias), provides education on the potential harm of treating asymptomatically elevated BPs, and suggests alternative procedures (e.g., monitoring BP more frequently). At the end of the study, three specific pieces of knowledge needed to conduct a larger, adequately powered randomized clinical trial will be obtained. First, how much does ACT-BP reduce antihypertensive medication intensification? Second, what refinements will improve its effectiveness? Third, what is the rate of the composite outcome in the intervention and control units?

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •At the unit level: Medical units that do not typically care for patients requiring step-down care.

Exclusion Criteria

  • •Patients less than 18
  • •Patients experiencing hypertensive emergencies or cardiac symptoms
  • •Patients with active cardiovascular events, such as
  • •Non-ST-elevation
  • •Myocardial infarction
  • •End-stage renal disease
  • •Patients on dialysis
  • •Those with acute decompensated heart failure
  • •3. Patients on the unit for more than 10 days
  • •4. Patients transferred in after being in the intensive care unit (ICU)
  • •5. Pregnant and post-partum women
  • •6. Patients discharged within 24 hours of admission
  • •7. Patients whose systolic BP remains below 160 mmHg during hospitalization.

Arms & Interventions

Intervention Arm

Experimental

The ACT-BP protocol will be implemented in the intervention units. First, the study team will implement an order on the unit that prompts the nurses to follow the ACT-BP algorithm when a patient has an asymptomatic elevated BP between 160mmHg and 199mmHg. This protocol does not apply to patients who are experiencing hypertensive emergencies or cardiac symptoms. To increase adherence to the ACT-BP protocol, knowledge related to treating the potential underlying causes of an asymptomatically elevated BP and the current state of the evidence will be shared through posters, information sheets and knowledge sessions.

At the the intervention hospital, the study team will provide caregivers (including physicians) with knowledge related to the state of the evidence for treating asymptomatically elevated BPs through emails, information sheets and one-pagers.

Intervention: ACT-BP Intervention (Other)

Control Arm

No Intervention

In the control units, care will continue as usual.

At the the control hospital, caregivers (including physicians) will receive knowledge related to the state of the evidence for treating asymptomatically elevated BPs through an email.

Outcomes

Primary Outcomes

Primary Outcome

Time Frame: From date of first elevated BP reading until the end of hospitalization, assessed up to 13 months.

The number of new orders for antihypertensive medications or increased doses of an antihypertensive medication for patients who experience an elevated systolic BP (≥160 mmHg and ≤199 mmHg).

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Elizabeth Pfoh
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Elizabeth Pfoh

Staff/Associate Professor of Medicine

The Cleveland Clinic

Study Sites (2)

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