Back to resultsInstruction to Compress Chest Approximately 6-7cm for Healthcare Provider in Hospital
Primary Purpose
Cardiac Arrest
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Education of chest compression depth
Sponsored by
About this trial
This is an interventional basic science trial for Cardiac Arrest focused on measuring Cardiopulmonary Resuscitation
Eligibility Criteria
Inclusion Criteria:
- Medical students, Healthy
Exclusion Criteria:
- Heart, wrist, and low back disease
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
5-6cm Chest compression depth
6-7cm chest compression depth
Arm Description
Control group is trained for 5-6cm Chest compression depth during education. Depth 5-6cm, Rate 100-120/min, Full chest recoil
Experimental group is trained for 6-7cm Chest compression depth during education. Depth 6-7cm, Rate 100-120/min, Full chest recoil
Outcomes
Primary Outcome Measures
Change of Chest compression depth at 4 weeks
Secondary Outcome Measures
Change of Chest compression rate at 4 weeks
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01936402
Brief Title
Instruction to Compress Chest Approximately 6-7cm for Healthcare Provider in Hospital
Official Title
Novel Instruction to Perform Chest Compression Approximately 6-7cm for Healthcare Provider Improves Chest Compression Depth During Cardiopulmonary Resuscitation in Hospital.
Study Type
Interventional
2. Study Status
Record Verification Date
September 2013
Overall Recruitment Status
Completed
Study Start Date
February 2013 (undefined)
Primary Completion Date
February 2013 (Actual)
Study Completion Date
April 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Jaehoon Oh
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Unlikely the other element for high quality chest compression during Cardiopulmonary resuscitation(i.e. compression rate, chest recoil, hand position), chest compression depth (CCD) is influenced by surface on which the patient is placed, especially in hospital. For solving this problem, to place the patient on rigid surface, use a backboard that might decrease the mattress compression, receive a feedback that reflects the mattress compression depth (MCD) using dual accelerometer or magnetic sensor have been proposed. As the other solution, we hypothesized that training of 6-7cm CCD for healthcare providers improve accurate CCD during cardiopulmonary resuscitation when manikin is placed on mattress in hospital.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Arrest
Keywords
Cardiopulmonary Resuscitation
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
66 (Actual)
8. Arms, Groups, and Interventions
Arm Title
5-6cm Chest compression depth
Arm Type
Experimental
Arm Description
Control group is trained for 5-6cm Chest compression depth during education.
Depth 5-6cm, Rate 100-120/min, Full chest recoil
Arm Title
6-7cm chest compression depth
Arm Type
Experimental
Arm Description
Experimental group is trained for 6-7cm Chest compression depth during education.
Depth 6-7cm, Rate 100-120/min, Full chest recoil
Intervention Type
Behavioral
Intervention Name(s)
Education of chest compression depth
Intervention Description
An American Heart Association Basic Life Support faculty educated each participant in Experimental group a standard 30-min lecture and hands- on practice for chest compression without ventilation using manikin on the floor according to 5-6cm or 6-7cm chest compression depth
Primary Outcome Measure Information:
Title
Change of Chest compression depth at 4 weeks
Time Frame
1 hour and 4weeks later after education
Secondary Outcome Measure Information:
Title
Change of Chest compression rate at 4 weeks
Time Frame
1 hour and 4weeks later after education
Other Pre-specified Outcome Measures:
Title
Change of number of Chest decompression at 4 weeks
Time Frame
1 hour and 4weeks later after education
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Medical students, Healthy
Exclusion Criteria:
Heart, wrist, and low back disease
12. IPD Sharing Statement
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Instruction to Compress Chest Approximately 6-7cm for Healthcare Provider in Hospital
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