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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02642744
Other study ID # 823366
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2015
Est. completion date December 2023

Study information

Verified date February 2024
Source University of Pennsylvania
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will examine if the attending nurse model will enhance critical patient-centered elements of care that will in turn improve patient education and shared decision-making, medication adherence, stroke-related health literacy, and reduce early readmissions to ultimately yield improved patient quality of life. Our primary objective is to determine whether the attending nurse model of care improves stroke patients' health at 7 days, 30 days, and 90 days after hospital discharge as assessed through questionnaires.


Recruitment information / eligibility

Status Completed
Enrollment 670
Est. completion date December 2023
Est. primary completion date September 30, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - > 18 years of age - Admission to the Hospital of the University of Pennsylvania Vascular Neurology service - Incident or recurrent: - Ischemic stroke: focal neurological deficit of likely ischemic vascular origin - Intracerebral hemorrhage: blood seen on initial head CT - Transient Ischemic attack: focal neurological deficit of likely ischemic vascular origin that has clinically resolved Exclusion Criteria: - Pregnancy - Comfort or hospice care - Severe dementia prior to stroke - Non-communicative and have no family/social support

Study Design


Intervention

Other:
Nursing care model
Subjects will be randomized into either the attending nursing model of care vs the standard nursing model

Locations

Country Name City State
United States Hospital of the University of Pennsylvania Philadelphia Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
University of Pennsylvania

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Stroke Patient Education Retention Tool measures patient knowledge about stroke 90 days
Primary Medication Compliance medication adherence measurement 90 Days
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