Recruitment

Recruitment Status
Enrolling by invitation
Estimated Enrollment
Same as current

Summary

Conditions
  • Engagement, Patient
  • Stroke
  • Stroke Hemorrhagic
  • Stroke Sequelae
  • Stroke Acute
  • Stroke Ischemic
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: Pragmatic randomized trial of 18 clinical sites in the United States; randomization is by clinical site.Masking: Single (Outcomes Assessor)Masking Description: Primary outcomes will be assessed by telephone at 3, 6, 12, and 24 months by C3FIT's Statistical and Data Coordinating Center (SDCC) Survey Research Unit (SRU) at the University of Alabama Birmingham (UAB). Research staff at the SRU will be masked to treatment arm.Primary Purpose: Health Services Research

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT04000971
Collaborators
  • Patient-Centered Outcomes Research Institute
  • University of Alabama at Birmingham
Investigators
Principal Investigator: Kenneth Gaines, MD Vanderbilt University Medical Center Principal Investigator: Barry Jackson Principal Investigator: George Howard, DrPH University of Alabama at Birmingham