Self-Management in Stroke Survivors

This study is currently recruiting participants. (see Contacts and Locations)
Verified October 2013 by University of Minnesota - Clinical and Translational Science Institute
Sponsor:
Collaborator:
Berman Center for Outcomes and Clinical Research
Information provided by (Responsible Party):
University of Minnesota - Clinical and Translational Science Institute
ClinicalTrials.gov Identifier:
NCT01875094
First received: May 29, 2013
Last updated: October 17, 2013
Last verified: October 2013

May 29, 2013
October 17, 2013
October 2012
December 2013   (final data collection date for primary outcome measure)
Rate of blood pressure control into guideline recommended ranges [ Time Frame: 3 months ] [ Designated as safety issue: No ]
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.
Same as current
Complete list of historical versions of study NCT01875094 on ClinicalTrials.gov Archive Site
  • Medication Compliance [ Time Frame: 3 months ] [ Designated as safety issue: No ]
    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 [ Time Frame: 3 months ] [ Designated as safety issue: No ]
    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.
Same as current
Not Provided
Not Provided
 
Self-Management in Stroke Survivors
Promoting Self-Management in Stroke Survivors Using Health IT

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

Not Provided
Interventional
Phase 1
Phase 2
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind (Subject)
Primary Purpose: Health Services Research
  • Stroke
  • Hypertension
Other: Self-Management / MTM using Health IT
  • Experimental: Self-Management / MTM via Health IT
    Stroke survivors are trained to measure and enter BP into an online health management tool
    Intervention: Other: Self-Management / MTM using Health IT
  • No Intervention: Usual Care
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
60
December 2013
December 2013   (final data collection date for primary outcome measure)

Inclusion Criteria:

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

Exclusion Criteria:

-Cannot use the health-IT system

Both
40 Years to 75 Years
No
United States
 
NCT01875094
1212M25581, R21HS021794
Yes
University of Minnesota - Clinical and Translational Science Institute
University of Minnesota - Clinical and Translational Science Institute
Berman Center for Outcomes and Clinical Research
Not Provided
University of Minnesota - Clinical and Translational Science Institute
October 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP