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

University of Michigan logo

University of Michigan

Status

Completed

Conditions

Hypertension
Stroke

Treatments

Behavioral: Text messaging

Study type

Interventional

Funder types

Other

Identifiers

NCT02301455
HUM00091668

Details and patient eligibility

About

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.

Enrollment

104 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

104 participants in 3 patient groups

Control, Not hypertensive
No Intervention group
Description:
Participants who after 3 weeks do not have high blood pressure or are not responsive to text messages.
Text messages, hypertensive
Experimental group
Description:
Participants who after 3 weeks have high blood pressure and are responsive to text messages, who are then randomized to receive text messages.
Treatment:
Behavioral: Text messaging
No text messages, hypertensive
No Intervention group
Description:
Participants who after 3 weeks have high blood pressure and are responsive to text messages, who are then randomized to not receive text messages.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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