Emergency Department Home Blood Pressure Monitoring and BpTRU Study

NCT ID: NCT02217059

Last Updated: 2017-11-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

105 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-08-31

Study Completion Date

2017-07-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this study is to evaluate the Congruence of Emergency Department (ED) Attendings' Predictions of Hypertension with Results of Home Blood Pressure Monitoring.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Evaluate the Congruence of Emergency Department (ED) Attendings' Predictions of Hypertension with Results of Home Blood Pressure Monitoring \& evaluate reliability of ED measured elevated blood pressure compared to the BpTRU

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Hypertension

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Emergency Medical Services Emergency Care Hypertension BpTRU Blood pressure

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Prehypertension

Using the JNC7 definition

No interventions assigned to this group

Stage I Hypertension

Using the JNC7 definition

No interventions assigned to this group

Stage II Hypertension

Using the JNC7 definition

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* One elevated blood pressure greater than 120 systolic and/or 80 diastolic
* BpTRU device blood pressure greater than 120 systolic and/or 80 diastolic while in ED

Exclusion Criteria

* Prior history of hypertension
* Currently on antihypertensives or receiving prescription on discharge
* Pregnancy
* History of atrial fibrillation
* Dialysis patient
* Nursing home or rehabilitation center resident
* Admitted
* Moving out of the area in next 30 days
* Substance abuse
* Prisoner
* Presenting for psychiatric complaint requiring constant observation
* Inability to give informed consent (intoxicated, altered, non-English speaking)
* Presenting with symptoms of hypertensive emergency
* Inability to demonstrate adequate use of the home blood pressure device in the ED
* Arm circumference less than 9 inches or greater than 17 inches
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Rhode Island Hospital

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Rhode Island Hospital

Providence, Rhode Island, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

UEMF0000

Identifier Type: -

Identifier Source: org_study_id