UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000058002 |
|---|---|
| Receipt number | R000066302 |
| Scientific Title | Examination of effective teaching methods in BLS (Basic life support) training |
| Date of disclosure of the study information | 2025/05/28 |
| Last modified on | 2025/05/28 15:17:43 |
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Basic information
Public title
Examination of effective teaching methods in BLS (Basic life support) training
Acronym
Examination of effective teaching methods in BLS (Basic life support) training
Scientific Title
Examination of effective teaching methods in BLS (Basic life support) training
Scientific Title:Acronym
Examination of effective teaching methods in BLS (Basic life support) training
Region
| Japan |
Condition
Condition
cardiac arrest
Classification by specialty
| Dental medicine |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The purpose of this study is to compare the educational effects of three groups: monitor group, instructor group, and monitor + instructor group, in order to search for factors that improve chest compressions and chest compression rhythm. By comparing and examining each evaluation item, we will examine the usefulness of each teaching method and consider effective self-study methods. We believe that this study is academically significant because it allows us to explore better educational methods.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Chest compression depth
Chest compression rhythm
Key secondary outcomes
Psychological state, questionnaire, recoil, compression time ratio, effective compression, CCF (Chest Compression Fraction), effective ventilation
Base
Study type
Interventional
Study design
Basic design
Parallel
Randomization
Randomized
Randomization unit
Individual
Blinding
Open -no one is blinded
Control
No treatment
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
3
Purpose of intervention
Educational,Counseling,Training
Type of intervention
| Maneuver |
Interventions/Control_1
Self-study using monitors (monitor feedback)
Interventions/Control_2
Traditional verbal instruction (instructor feedback)
Interventions/Control_3
Self-study using monitors and traditional oral instruction
Interventions/Control_4
Interventions/Control_5
Interventions/Control_6
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10
Eligibility
Age-lower limit
| Not applicable |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
Kagoshima University School of Dentistry students taking part in the 1 Poly practical training course
Key exclusion criteria
1. People with injuries to the upper limbs
2. Women who are pregnant, may be pregnant, have given birth within 28 days, or are breastfeeding
3. Subjects who are deemed to have difficulty participating in the study due to mental illness or psychiatric symptoms
4. Other subjects who a dentist judges to be unsuitable for the study
Target sample size
55
Research contact person
Name of lead principal investigator
| 1st name | Kaoru |
| Middle name | |
| Last name | Yamashita |
Organization
Field of Oral and Maxillofacial Rehabilitation, Advanced Therapeutics Course, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima
Division name
Department of Dental Anesthesiology
Zip code
890-8520
Address
8-35-1 Sakuragaoka, Kagoshima City, Kagoshima Prefecture
TEL
099-275-6288
crmc@m2.kufm.kagoshima-u.ac.jp
Public contact
Name of contact person
| 1st name | Kaoru |
| Middle name | |
| Last name | Yamashita |
Organization
Graduate School of Medical and Dental Sciences, Kagoshima University
Division name
Department of Dental Anesthesiology
Zip code
890-8520
Address
Kagoshima University, 8-35-1 Sakuragaoka, Kagoshima 890-8544, Japan.
TEL
099-275-5354
Homepage URL
crmc@m2.kufm.kagoshima-u.ac.jp
Sponsor or person
Institute
Kagoshima University
Institute
Department
Personal name
Funding Source
Organization
Kagoshima University
Organization
Division
Category of Funding Organization
Other
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Kagoshima University Sakuragaoka District Clinical Research Ethics Committee
Address
8-35-1 Sakuragaoka, Kagoshima City, Kagoshima Prefecture
Tel
099-275-5354
crmc@m2.kufm.kagoshima-u.ac.jp
Secondary IDs
Secondary IDs
NO
Study ID_1
Org. issuing International ID_1
Study ID_2
Org. issuing International ID_2
IND to MHLW
Institutions
Institutions
Other administrative information
Date of disclosure of the study information
| 2025 | Year | 05 | Month | 28 | Day |
Related information
URL releasing protocol
Publication of results
Unpublished
Result
URL related to results and publications
Number of participants that the trial has enrolled
Results
Results date posted
Results Delayed
Results Delay Reason
Date of the first journal publication of results
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
Plan to share IPD
IPD sharing Plan description
Progress
Recruitment status
Open public recruiting
Date of protocol fixation
| 2025 | Year | 04 | Month | 01 | Day |
Date of IRB
| 2025 | Year | 04 | Month | 01 | Day |
Anticipated trial start date
| 2025 | Year | 04 | Month | 30 | Day |
Last follow-up date
| 2028 | Year | 03 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2025 | Year | 05 | Month | 28 | Day |
Last modified on
| 2025 | Year | 05 | Month | 28 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000066302
