- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05814120
Effectiveness of Basic Life Support Training for Rural Community Dwelling Elderly
April 3, 2023 updated by: Ching-Ching Su, Chang Gung University of Science and Technology
Chang Gung University of Science and Technology
The goal of this pre-post study is to test the effectiveness of basic life support (BLS) training for rural community-dwelling Elderly.
The main question it aims to answer are can the training program tailored for rural elderly improve basic life support knowledge, attitude, and skills?
Participants will receive an innovative BLS training program.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
218
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Chiayi City, Taiwan
- Chang Gung University of Science and Technology
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
age older than 65-year-old, intact cognition, coordinated activities, and no history of severe cardiovascular disease, asthma, or lower extremity impairment.
Exclusion Criteria:
severe visual and hearing impairment, impractical to move, and mental illness.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Experimental arm
Geriatric-specific BLS training program
|
BLS training program was in accordance with the 2020 AHA cardiopulmonary resuscitation (CPR) guidelines.
The BLS training program adopts 4D teaching techniques, namely description (Describe), demonstration (Demo), implementation (Do), feedback (Debriefing).
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Changes to the BLS Knowledge Questionnaire
Time Frame: Completion by study, average 60 minutes.
|
The BLS knowledge assessment consisted of 10 questions with structured "yes" or "no" answers and was based on expert consensus from the AHA (AHA, 2020).
Scores were calculated based on the number of correct answers given, with higher scores indicating a greater understanding of BLS.
|
Completion by study, average 60 minutes.
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Changes to the BLS attitude Questionnaire
Time Frame: Completion by study, average 60 minutes.
|
The BLS attitude questionnaire contained five statements with five-point Likert-type scale responses ranging from "strongly agree" to "strongly disagree."
Positive attitudinal answers awarded higher scores.
|
Completion by study, average 60 minutes.
|
The observable BLS skill checklist
Time Frame: Completion by study, average 60 minutes.
|
The observable BLS skill checklist included ten steps related to BLS practices, such as assessing responsiveness, calling for help, and using an AED.
The researcher completed the checklist and rated each step on a 2-point scale, with higher scores indicating better BLS practices.
|
Completion by study, average 60 minutes.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 1, 2021
Primary Completion (Actual)
August 31, 2022
Study Completion (Actual)
August 31, 2022
Study Registration Dates
First Submitted
January 31, 2023
First Submitted That Met QC Criteria
April 3, 2023
First Posted (Actual)
April 14, 2023
Study Record Updates
Last Update Posted (Actual)
April 14, 2023
Last Update Submitted That Met QC Criteria
April 3, 2023
Last Verified
April 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 201600580B0
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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