Coordinated, Collaborative, Comprehensive, Family-based, Integrated, Technology-enabled Stroke Care
Last updated on July 2021Recruitment
- 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