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BE FAST vs. FAST: A Study in the General Public.

BE FAST vs. FAST: A Randomized Trial Comparing Retention of Stroke Symptoms Between Two Mnemonics in the General Public.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06152016
Acronym
BFF
Enrollment
174
Registered
2023-11-30
Start date
2021-11-20
Completion date
2023-06-23
Last updated
2024-10-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Keywords

BE-FAST, FAST

Brief 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.

Interventions

OTHERBE-FAST

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

OTHERFAST

This intervention includes those randomized to the education with the FAST mnemonic.

Sponsors

BayCare Health System
CollaboratorOTHER
Aurora BayCare Medical Center
CollaboratorOTHER
Wake Forest University Health Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Recall Visit 160 minutesNumber/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.

Secondary

MeasureTime frameDescription
Recall Rate Symptom30 daysTotal number of stroke symptoms that were accurately recalled by the participants
Recall Participant Percentage30 daysNumber/percentage of participants able to recall all the symptoms included in the mnemonic
Retention Rate Symptom30 daysRetention rate of each stroke symptom in the mnemonic
Common Recall Participant Percentage30 daysNumber/percentage of participants able to recall the more common symptoms of each mnemonic (Facial weakness, arm weakness and speech difficulties)
Retention per Professional Background30 daysCompare participants with medical vs. non-medical professional backgrounds and explore whether there are any group differences in retention rates.
Patrial Recall Participant Percentage30 daysNumber/percentage of participants able to recall 2 or more symptoms of the FAST mnemonic or 3 or more of the BE-FAST mnemonic.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026