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Completed Not applicable Interventional Accepts healthy volunteers

Dissemination and Implementation of Stroke Prevention Looking at the Care Environment

ClinicalTrials.gov ID: NCT04173026

Public ClinicalTrials.gov record NCT04173026. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 10:26 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Dissemination and Implementation of Stroke Prevention Looking at the Care Environment (DISPLACE) Part 3

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The Dissemination and Implementation of Stroke Prevention Looking at the Care Environment (DISPLACE) study is a multi-center, national, National Heart, Lung and Blood Institute (NHLBI)-funded grant to look at the real-world implementation of stroke prevention guidelines (STOP Protocol) in which transcranial Doppler (TCD), a measure of cerebral blood vessel velocity, is used to screen for stroke risk in children ages 2-16 with sickle cell anemia (SCA). Part 3 of the DISPLACE study is an implementation clinical trial designed to test novel implementation strategies with the goal of improving adherence and implementation of stroke screening. 16 of the lowest scoring implementation rates from DISPLACE Part 1 will participate in DISPLACE Part 3. All original 28 sites from DISPLACE Parts 1 and 2 will receive a patient and provider educational intervention including a re-branding of the TCD as "Sickle Stroke Screen" with a new infographic and educational materials. The 16 sites with moving to Part 3 will be provided a Provider reminder strategy, which is a web based application designed to remind providers of when patients are due for their Sickle Stroke Screen. These 16 sites will be randomized and 8 will be given an additional Patient Communication Strategy. These sites will have a single designed coordinator with whom patients will communicate with about scheduling, rescheduling, and any other questions regarding their Sickle Stroke Screen. Upon completion, data will be analyzed to compare those who have had TCD screenings done appropriately and those who did not as well as the overall effect of the multi level interventions on the changes in TCD rates.

Study identification

NCT ID
NCT04173026
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
16 participants

Conditions and interventions

Eligibility (public fields only)

Age range
2 Years to 7 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 3, 2020
Primary completion
Jan 31, 2023
Completion
Jun 29, 2023
Last update posted
Jul 2, 2023

2020 – 2023

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
13
Facility City State ZIP Site status
Arkansas Children's Research Institute Little Rock Arkansas 72202
UCSF Benioff Children's Hospital Oakland Oakland California 94609
Nemours Center for Cancer & Blood Disorders Wilmington Delaware 19803
Children's National Medical Center Washington D.C. District of Columbia 20010
Howard University Hospital Washington D.C. District of Columbia 20060
Broward Health Medical Center Fort Lauderdale Florida 33316
University of Florida Health Shands Children's Hospital Gainesville Florida 32608
University of Miami Miami Florida 33136
Children's Heathcare of Atlanta Atlanta Georgia 30322
University of Illinois at Chicago Chicago Illinois 60607
SSM Health Cardinal Glennon Children's Hospital St Louis Missouri 63104
St. Louis Children's Hospital St Louis Missouri 63110
Columbia University Medical Center New York New York 10032
Vidant Medical Center Greenville North Carolina 27834
Vanderbilt Children's Hospital Nashville Tennessee 37232

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04173026, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 2, 2023 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04173026 live on ClinicalTrials.gov.

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