CClinicalTrials.gg
Status unknownNCT04699409Updated Jan 7, 2021

The Comparison of Educational Effectiveness Between FAST and STROKE 112 in Yunlin Community

An interventional study of stroke educational campaign: FAST and stroke educational campaign: STROKE 112 in Stroke, Cardiovascular, sponsored by National Taiwan University Hospital. Status unknown at 1 site in Taiwan. Open to participants aged 20 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-01-07.

Sponsored by National Taiwan University Hospital · Not applicable, Interventional, and Health services research

The sponsor has not verified this record recently (last verified Jan 2021), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
300
Allocation
Randomized
Ages
20 Years and older
Sex
All
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Study summary

FAST and Stroke-112 are two campaigns to reduce the emergency room arrival time of stroke patients. No study has evaluated the effectiveness of these campaigns. This study aimed to compare recalling capacity of people in these two campaigns.

Read the detailed description

Cerebral vascular accidents have been one of the leading causes of death in Taiwan in recent years. In the modern medical system, treatment for hyperacute stroke including intravenous thrombolysis and intra-arterial thrombectomy. The faster patient received treatment, the better outcome he has.

Prehospital delay of acute stroke treatment has been an important issue in modern medical system. Awareness of stroke symptoms and calling for medical help immediately is the most important part of stroke health education. The most used educational campaign is FAST.

In recent years, there is another stroke educational campaign called STROKE 112. Previous study had showed it has greater acceptance, since the number is easier to remember then letter, especially in non-English speaking countries.

The investigators had conducted a hospital-based randomized study in 2019, which revealed that STROKE 112 had similar, but not superior effectiveness with FAST. However, more study is needed for community-based population.

This study will compare and explore the effectiveness of two stroke educational campaigns, FAST and STROKE 112, on community-based population by using the questionnaire, in Yunlin, Taiwan. The result will been compared and analyzed with previous study, help us modify and enhance our current stroke educational program, shorten the prehospital delay, and improve outcomes of patients with acute stroke.

The subjects will be randomized into either group: FAST or STROKE 112. Then the investigator will give a 15min eduacation. The evaluation will be arranged 5 days and 30 days after the first education, and the outcome is the recalling capacity of the stroke symptoms in the educational campaign.

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Conditions studied

  • Stroke, Cardiovascular
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In context

Stroke

7,286 studies on the registry are indexed under Stroke; 2,007 are open to participants now.

This study's planned enrollment of 300 is above the median of 50 across 5,369 interventional studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

National Taiwan University Hospital is the lead sponsor of 2,563 studies on the registry; 569 are open to participants now.

Of its 11 completed or terminated interventional studies of FDA-regulated products, 2 (18%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • age ≥ 20
  • individuals who could speak either Mandarin or Taiwanese as their mother tongue

Exclusion criteria

Exclusion Criteria:

  • individuals who could not understanding the education campaign(ex. dementia, aphasia)
  • individuals who were previously aware about either campaign
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Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
300 participants (estimated)

Study arms

  • Experimental
    FAST

    stroke education: FAST

    Other: stroke educational campaign: FAST

  • Experimental
    STROKE 112

    stroke education: STROKE 112

    Other: stroke educational campaign: STROKE 112

Interventions

  • Otherstroke educational campaign: FAST

    After randomization, study staff provided 15-minute education on the selected campaign to each individual participant using educational pictures.

  • Otherstroke educational campaign: STROKE 112

    After randomization, study staff provided 15-minute education on the selected campaign to each individual participant using educational pictures.

06

What researchers measure

Primary outcomes

  1. The recalling capacity of the stroke symptoms mentioned in each campaign

    Compare recalling capacity of people in these two campaigns: uneven face, weak arm, slurred speech. If the patient could recall one symptom, then he get 1 score. Total score is 3(which means the subject can recall all three symptoms)

    Time frame: 5 days

  2. The recalling capacity of the stroke symptoms mentioned in each campaign

    Compare recalling capacity of people in these two campaigns: uneven face, weak arm, slurred speech. If the patient could recall one symptom, then he get 1 score. Total score is 3(which means the subject can recall all three symptoms)

    Time frame: 30 days

07

Study locations

1 of 1 sites recruiting
  • National Taiwan University Hospital Yunlin Branch
    Douliu, Taiwan
    • Dr. Tsai · Contact · +886055323911
    Recruiting
08

References and documents

Individual participant data

Plan to share: No — No plan to share IPD

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 7, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04699409
Lead sponsor
National Taiwan University Hospital
Responsible party
Sponsor
First posted
Jan 7, 2021
Start date
Jan 1, 2021 (estimated)
Primary completion
Oct 31, 2021 (estimated)
Completion
Dec 31, 2021 (estimated)
Last update
Jan 7, 2021

Study contacts

YiTe Tsai, Bachelor
Contact
duckeryite@gmail.com
+886972655687
YiTe Tsai, Bachelor
principal investigator · National Taiwan University Hospital Yunlin Branch

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jan 2021. You cannot join it, but the record below documents what was studied.

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