Self-Management in Stroke Survivors

Phase 1

Completed

• Conditions: Stroke; Hypertension
• Interventions: Other: Self-Management / MTM using Health IT

• Registration Number: NCT01875094
• Lead Sponsor: University of Minnesota

Brief Summary

This is a feasibility study of using health-IT to promote self-management of risk factors in stroke survivors.

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2012-10
• Study First Submitted: 2013-05-29
• Study First Submitted QC: 2013-06-10
• Study First Posted: 2013-06-11
• Primary Completion: 2016-03
• Study Completion: 2016-03
• Status Verified: 2016-06
• Last Update Submitted: 2016-06-23
• Last Update Posted: 2016-06-24

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 56

Inclusion Criteria

• Acute Stroke Survivors and their caregivers
• English speaking
• History of hypertension

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Exclusion Criteria

-Cannot use the health-IT system

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Self-Management / MTM via Health IT	Self-Management / MTM using Health IT	Stroke survivors are trained to measure and enter BP into an online health management tool

Primary Outcome Measures

Name	Time	Method
Rate of blood pressure control into guideline recommended ranges	3 months	The American Heart Association/American Stroke Association (AHA/ASA) have cited the JNC-7 in their guidelines to define normal blood pressure as \< 120/80. We will use these guidelines and examine rates (percentage of subjects) of blood pressure control in intervention vs. usual care group.

Secondary Outcome Measures

Name	Time	Method
Medication Compliance	3 months	Percent of subjects who have discontinued one or more of the blood pressure medications on their own (i.e. without medical direction) in the intervention vs. usual care group.
Use of online tool	3 months	Ease of online health management tool use will be operationalized as the percent of subjects in the intervention group who measure their BP and enter it online at least 75% of the study period, 50% of the study period and those with 25% or less of the study period.

Trial Locations

Locations (1)

University_of_Minnesota; 🇺🇸 Minneapolis, Minnesota, United States