The Comparison of Educational Effectiveness Between FAST and STROKE 112 in Yunlin Community
Primary Purpose
Stroke, Cardiovascular
Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
stroke educational campaign: FAST
stroke educational campaign: STROKE 112
Sponsored by
About this trial
This is an interventional health services research trial for Stroke, Cardiovascular
Eligibility Criteria
Inclusion Criteria:
- age ≥ 20
- individuals who could speak either Mandarin or Taiwanese as their mother tongue
Exclusion Criteria:
- individuals who could not understanding the education campaign(ex. dementia, aphasia)
- individuals who were previously aware about either campaign
Sites / Locations
- National Taiwan University Hospital Yunlin BranchRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
FAST
STROKE 112
Arm Description
stroke education: FAST
stroke education: STROKE 112
Outcomes
Primary Outcome Measures
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)
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)
Secondary Outcome Measures
Full Information
NCT ID
NCT04699409
First Posted
January 4, 2021
Last Updated
January 6, 2021
Sponsor
National Taiwan University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04699409
Brief Title
The Comparison of Educational Effectiveness Between FAST and STROKE 112 in Yunlin Community
Official Title
The Comparison of Educational Effectiveness Between FAST and STROKE 112 in Yunlin Community
Study Type
Interventional
2. Study Status
Record Verification Date
January 2021
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2021 (Anticipated)
Primary Completion Date
October 31, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Taiwan University Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief 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.
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Cardiovascular
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
300 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
FAST
Arm Type
Experimental
Arm Description
stroke education: FAST
Arm Title
STROKE 112
Arm Type
Experimental
Arm Description
stroke education: STROKE 112
Intervention Type
Other
Intervention Name(s)
stroke educational campaign: FAST
Intervention Description
After randomization, study staff provided 15-minute education on the selected campaign to each individual participant using educational pictures.
Intervention Type
Other
Intervention Name(s)
stroke educational campaign: STROKE 112
Intervention Description
After randomization, study staff provided 15-minute education on the selected campaign to each individual participant using educational pictures.
Primary Outcome Measure Information:
Title
The recalling capacity of the stroke symptoms mentioned in each campaign
Description
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
Title
The recalling capacity of the stroke symptoms mentioned in each campaign
Description
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
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
age ≥ 20
individuals who could speak either Mandarin or Taiwanese as their mother tongue
Exclusion Criteria:
individuals who could not understanding the education campaign(ex. dementia, aphasia)
individuals who were previously aware about either campaign
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
YiTe Tsai, Bachelor
Phone
+886972655687
Email
duckeryite@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
YiTe Tsai, Bachelor
Organizational Affiliation
National Taiwan University Hospital Yunlin Branch
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Taiwan University Hospital Yunlin Branch
City
Douliu
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dr. Tsai
Phone
+886055323911
Ext
55687
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
No plan to share IPD
Learn more about this trial
The Comparison of Educational Effectiveness Between FAST and STROKE 112 in Yunlin Community
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