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Community Study to Reduce High Blood Pressure Through Text Messaging (REACH OUT)

University of Michigan logo

University of Michigan

Status

Completed

Conditions

Hypertension
Stroke

Treatments

Behavioral: Text Messaging

Study type

Interventional

Funder types

Other

Identifiers

NCT02664610
GO13884

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 significantly more prevalent in African Americans compared to European Americans. Importantly, hypertension is a modifiable stroke risk factor.

This proposal will use a community-based participatory research approach to perform a randomized trial of a mobile phone text-messaging intervention to reduce high blood pressure in an urban African American community in Flint, Michigan.

Full description

This is a randomized controlled trial of text messaging and blood pressure self-monitoring to reduce blood pressure.

Enrollment

94 patients

Sex

All

Ages

18 to 110 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult (>18 y/o) participants with BP ≥140/90 who have mobile phones with text-messaging capability.

Exclusion criteria

  • Adult who is illiterate, non-English speaking, pregnant, incarcerated/ institutionalized resident, or has a pre-existing condition that makes follow-up for 6 months unlikely.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

94 participants in 2 patient groups

No text messages, hypertensive
No Intervention group
Description:
Participants who have high blood pressure, who are randomized to health information (do not receive text messages).
Text messages, hypertensive
Experimental group
Description:
Participants who have high blood pressure, who are randomized to receive text messages.
Treatment:
Behavioral: Text Messaging

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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