Basic Cardiac Life SupportNCT02964832
Assessment of Chest Compression Depth Obtained Using the Smartphone Application as an Educational Tool With New Attachment Device
A study testing Grasp method, Armband-in-hand method and Armband-on-arm method in people with Basic Cardiac Life Support, run by Soonchunhyang University Hospital.
Trial summary
To improve the quality of CPR education, we want to assess the validity and reliability of the feedback depth measured by smartphone applications according to the smartphone attachment sites as an educational tool. However, in the prior study, armband method showed overestimated chest compression depth. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Basic Cardiac Life Support
- What is being tested?
- Grasp method, Armband-in-hand method and Armband-on-arm method
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 50 participants
- Where
- No sites listed yet
- Study dates
- Jan 2017to Jun 2017
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- BLS provider or instructor
Who cannot join
- one who has physical problem in chest compression
Trial locations and contacts
No sites are listed yet.
About this study
To improve the quality of CPR education, we want to assess the validity and reliability of the feedback depth measured by smartphone applications according to the smartphone attachment sites as an educational tool. However, in the prior study, armband method showed overestimated chest compression depth. The reason of the overestimation was analyzed that the weight of the smartphone amplified the inertial force to produce additional linear movement. In this study, we will make new device to fix the smartphone on the arm and on the hand and compare the chest compression depth between CPR manikin and smartphone application.
- Conditions
- Basic Cardiac Life Support
- Being tested
- Grasp method, Armband-in-hand method, Armband-on-arm method
- Keywords
- Basic Cardiac Life Support, Education, Feedback
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Grasp methodDevice
Armband-in-hand methodDevice
Armband-on-arm methodDevice
| Study group | Role | What they receive |
|---|---|---|
| PocketCPR;Grasp method | Active comparator | Subject grasp a smartphone in the hand and compress the chest of manikin. Receives: Device: Grasp method |
| PocketCPR;Armband-in-hand method | Active comparator | Grab the smartphone-contained-armband in hand when performing chest compression Receives: Device: Armband-in-hand method |
| PocketCPR;Armband-on-arm method | Active comparator | Fix the smartphone-contained-armband on upperarm when performing chest compression Receives: Device: Armband-on-arm method |
What is being measured
The primary outcome is the main question the study is designed to answer.
Assessment of validity of Chest compression depth by smartphone application,PocketCPR
Measured: Through study completion, average 4 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Nov 2016 (estimated)
- Study startJan 2017
- Primary completionMar 2017 (estimated)
- Study completionJun 2017 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Basic Cardiac Life SupportStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Diagnosis
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Enrolment
- 50 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Soonchunhyang University Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Joonbum Park, Soonchunhyang University Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02964832
- Sponsor's protocol ID
- JPark1601
- Status last verified
- Nov 2016
- First submitted
- 2 Nov 2016
- Last updated
- 16 Nov 2016
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 16 Nov 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Assessment of Chest Compression Depth Obtained Using the Smartphone Application as an Educational Tool With New Attachment Device
- ClinicalTrials.gov ID
- NCT02964832
- Acronym / sponsor ID
- JPark1601
- Conditions
- Basic Cardiac Life Support
- Keywords
- Basic Cardiac Life Support, Education, Feedback
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 50 participants (estimated)
- Lead sponsor
- Soonchunhyang University HospitalUniversity, hospital or other
- Study start
- Jan 2017
- Primary completion
- Mar 2017 (estimated)
- Study completion
- Jun 2017 (estimated)
- First posted
- 16 Nov 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
To improve the quality of CPR education, we want to assess the validity and reliability of the feedback depth measured by smartphone applications according to the smartphone attachment sites as an educational tool. However, in the prior study, armband method showed overestimated chest compression depth. The reason of the overestimation was analyzed that the weight of the smartphone amplified the inertial force to produce additional linear movement. In this study, we will make new device to fix the smartphone on the arm and on the hand and compare the chest compression depth between CPR manikin and smartphone application.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| PocketCPR;Grasp method | Active comparator | Device: Grasp methodSubject grasp a smartphone in the hand and compress the chest of manikin. |
| PocketCPR;Armband-in-hand method | Active comparator | Device: Armband-in-hand methodGrab the smartphone-contained-armband in hand when performing chest compression |
| PocketCPR;Armband-on-arm method | Active comparator | Device: Armband-on-arm methodFix the smartphone-contained-armband on upperarm when performing chest compression |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- BLS provider or instructor
Key exclusion criteria (1 listed)
- one who has physical problem in chest compression
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Grasp method | Device | PocketCPR;Grasp method |
| Armband-in-hand method | Device | PocketCPR;Armband-in-hand method |
| Armband-on-arm method | Device | PocketCPR;Armband-on-arm method |
Primary outcome
Assessment of validity of Chest compression depth by smartphone application,PocketCPR
Time frame: Through study completion, average 4 weeks
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Nov 2016.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Questions about this trial
What is this clinical trial studying?
A study testing Grasp method, Armband-in-hand method and Armband-on-arm method in people with Basic Cardiac Life Support, run by Soonchunhyang University Hospital.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 16 Nov 2016. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Joonbum Park, MD, PhD (82-2-709-9117, jesumania@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Assessment of validity of Chest compression depth by smartphone application,PocketCPR (time frame: Through study completion, average 4 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Nov 2016.