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REACH OUT: to Reduce High Blood Pressure in the Emergency Department

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02301455
Enrollment
104
Registered
2014-11-26
Start date
2014-10-31
Completion date
2015-08-31
Last updated
2018-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension, Stroke

Keywords

hypertension treatment, stroke prevention

Brief summary

One of the most powerful predictors of stroke is hypertension, with estimates of approximately 33% of adults in the United States experiencing this condition. Hypertension is very prevalent in the emergency department (ED), but significantly undertreated. The overall goal of this project is to develop a text messaging intervention to improve hypertension care in the ED. This will first be done by testing the feasibility of identifying hypertensive patients in the ED, and the response rate to text messages.

Interventions

BEHAVIORALText messaging

persistently hypertensive participants will be randomized to receive these tailored, motivational text messages

Sponsors

University of Michigan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult (≥18 y/o) * At least one BP of systolic blood pressure (SBP) ≥160 or a diastolic blood pressure (DBP) ≥100 or only BP performed prior to enrollment is SBP ≥160 or a DBP ≥100 (If the patient has repeated measurements after achieving Criteria 1, but prior to being enrolled, at least one of the repeat BP remains SBP ≥140 or a DBP ≥90) * Must have mobile phones with text-messaging capability * Likely to be discharged from the ED

Exclusion criteria

* Adult who is in an urgent condition * Unable to read * Non-English speaking * Incarcerated/ institutionalized resident * Pregnant, or has a pre-existing condition that makes follow-up for 4 months unlikely.

Design outcomes

Primary

MeasureTime frame
Proportion of people who respond to text messages and are persistently hypertensive3 weeks

Secondary

MeasureTime frameDescription
Change in systolic and diastolic blood pressure4 months
Feasibility of a screening algorithm4 monthsProportion of subjects recruited compared to proportion of subjects approached. Subject eligibility identified by screening algorithm.
Feasibility of subject follow-up mechanism4 monthsProportion of subjects responding to follow-up text messages
Mean group differences and standard deviations for systolic blood pressure4 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026