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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06152016
Other study ID # 19-807
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 20, 2021
Est. completion date June 23, 2023

Study information

Verified date November 2023
Source Aurora Health Care
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A randomized, blinded prospective study assessing retention of two stroke mnemonics (BE FAST and FAST) in the general public after receiving brief stroke education. Participants were randomized to one of two education arms and retention was tested at 3 different time intervals.


Recruitment information / eligibility

Status Completed
Enrollment 174
Est. completion date June 23, 2023
Est. primary completion date May 18, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Subject 18 years of age or older 2. Subject speaks English (Does not need interpreter) 3. Subject able to read English 4. Subject willing to provide a phone number for future follow up 5. Subject willing and agreeable to up to 2 phone follow up calls 6. Subject willing to provide verbal consent to participate Exclusion Criteria: 1. Subject non-English speaking (needs interpreter) 2. Subject has visual or hearing impairment 3. Subject has history of Dementia or a learning disability 4. Subject had stroke education within the past year 5. Subject had a previous stroke

Study Design


Related Conditions & MeSH terms


Intervention

Other:
BE-FAST
This intervention includes those randomized to the education with the BE-FAST mnemonic.
FAST
This intervention includes those randomized to the education with the FAST mnemonic.

Locations

Country Name City State
United States Aurora BayCare Medical Center Green Bay Wisconsin

Sponsors (3)

Lead Sponsor Collaborator
Aurora Health Care Aurora BayCare Medical Center, BayCare Health System

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Recall Visit 1 Number/percentage of participants in the FAST and BE-FAST groups at Visit 1 who accurately recall the mnemonic they were taught during the education session. 60 minutes
Secondary Retention Rate Symptom Retention rate of each stroke symptom in the mnemonic 30 days
Secondary Recall Rate Symptom Total number of stroke symptoms that were accurately recalled by the participants 30 days
Secondary Recall Participant Percentage Number/percentage of participants able to recall all the symptoms included in the mnemonic 30 days
Secondary Patrial Recall Participant Percentage Number/percentage of participants able to recall 2 or more symptoms of the FAST mnemonic or 3 or more of the BE-FAST mnemonic. 30 days
Secondary Common Recall Participant Percentage Number/percentage of participants able to recall the more common symptoms of each mnemonic (Facial weakness, arm weakness and speech difficulties) 30 days
Secondary Retention per Professional Background Compare participants with medical vs. non-medical professional backgrounds and explore whether there are any group differences in retention rates. 30 days
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