Cardiopulmonary ResuscitationNCT02175563
Tilt Cardiopulmonary Resuscitation With a Feedback Device
A study testing Audiovisual feedback from smartphone based app in people with Cardiopulmonary Resuscitation and Basic Cardiac Life Support, run by Hanyang University at 1 site in South Korea.
Trial summary
According to the European Resuscitation Council (ERC) Guidelines for patient to a depth of approximately 5-6 cm on a firm and flat surface when possible. However, Cardiopulmonary resuscitation (CPR) performers may need to continue the chest Resuscitation 2010, CPR performers should compress the sternum of a… Read more about this study
- Who is it for?
- Ages 18 to 65 yearsHealthy volunteers can take part
- Conditions the study is for
- Cardiopulmonary Resuscitation, Basic Cardiac Life Support
- What is being tested?
- Audiovisual feedback from smartphone based app
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 36 participants
- Where
- 1 siteSouth Korea
- Study dates
- Aug 2014to Aug 2014
- 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 to 65 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Healthy person
- > 18 years old
- Basic life support educated person
Who cannot join
- Cardiovascular disease
- Musculoskeletal disease
- Psychiatric disease
- Pregnant
- > 65 years old
Trial locations and contacts
1 site in 1 country.
About this study
According to the European Resuscitation Council (ERC) Guidelines for patient to a depth of approximately 5-6 cm on a firm and flat surface when possible. However, Cardiopulmonary resuscitation (CPR) performers may need to continue the chest Resuscitation 2010, CPR performers should compress the sternum of a compression in an oblique direction, such as in elevators. For a pregnant patient in cardiac arrest, the 2010 ERC Guidelines recommend that the performer place the patient in a left-lateral tilt of 15 - 30° using a firm wedge to support the pelvis and thorax because the pregnant uterus can compress the inferior vena cava. We hypothesized Smartphone based chest compression feedback app would improves quality of CPR in an angulated surface.
- Being tested
- Audiovisual feedback from smartphone based app
- Keywords
- Chest, Compression
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Audiovisual feedback from smartphone based appDevice
| Study group | Role | What they receive |
|---|---|---|
| Without feedback | No intervention | Participants compress the chest of the manikin without smartphone based feedback app. |
| With feedback | Experimental | Participants compress the chest of the manikin with a smartphone based feedback app. Receives: Device: Audiovisual feedback from smartphone based app |
What is being measured
The primary outcome is the main question the study is designed to answer.
Chest compression depth
To measure chest compression depth during 2 minutes
Measured: within the first 30 days after the end of recording
Chest compression rate
To measure the chest compression rate during 2 minutes
Measured: within the first 30 days after the end of recording
Secondary outcomes (1)
Accurate chest compression
To measure the percentage of accurate chest compressions (i.e. correct depth, hand position, and recoil) of total chest compressions during 2 minutes
Measured: within the first 30 days after the end of recording
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Jun 2014 (estimated)
- Study startAug 2014
- Primary completionAug 2014
- Study completionAug 2014
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cardiopulmonary ResuscitationStudies 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
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 36 participants (actual)
Sponsor and investigators
- Lead sponsor
- Hanyang University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Jaehoon Oh, Hanyang University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02175563
- Sponsor's protocol ID
- Tilt CPR
- Status last verified
- Aug 2014
- First submitted
- 25 Jun 2014
- Last updated
- 27 Aug 2014
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 27 Aug 2014. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Tilt Cardiopulmonary Resuscitation With a Feedback Device
- ClinicalTrials.gov ID
- NCT02175563
- Acronym / sponsor ID
- Tilt CPR
- Keywords
- Chest, Compression
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 36 participants (actual)
- Lead sponsor
- Hanyang UniversityUniversity, hospital or other
- Study start
- Aug 2014
- Primary completion
- Aug 2014 (actual)
- Study completion
- Aug 2014 (actual)
- First posted
- 26 Jun 2014 (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.
According to the European Resuscitation Council (ERC) Guidelines for patient to a depth of approximately 5-6 cm on a firm and flat surface when possible. However, Cardiopulmonary resuscitation (CPR) performers may need to continue the chest Resuscitation 2010, CPR performers should compress the sternum of a compression in an oblique direction, such as in elevators. For a pregnant patient in cardiac arrest, the 2010 ERC Guidelines recommend that the performer place the patient in a left-lateral tilt of 15 - 30° using a firm wedge to support the pelvis and thorax because the pregnant uterus can compress the inferior vena cava. We hypothesized Smartphone based chest compression feedback app would improves quality of CPR in an angulated surface.
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Without feedback | No intervention | –Participants compress the chest of the manikin without smartphone based feedback app. |
| With feedback | Experimental | Device: Audiovisual feedback from smartphone based appParticipants compress the chest of the manikin with a smartphone based feedback app. |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Healthy person
- > 18 years old
- Basic life support educated person
Key exclusion criteria (5 listed)
- Cardiovascular disease
- Musculoskeletal disease
- Psychiatric disease
- Pregnant
- > 65 years old
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 |
|---|---|---|
| Audiovisual feedback from smartphone based app | Device | With feedback |
Primary outcome
Chest compression depth
Time frame: within the first 30 days after the end of recording
To measure chest compression depth during 2 minutes
Chest compression rate
Time frame: within the first 30 days after the end of recording
To measure the chest compression rate during 2 minutes
1 secondary outcome
Accurate chest compression
Time frame: within the first 30 days after the end of recording
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Aug 2014.
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RACE-CARS - RAndomized Cluster Evaluation of Cardiac ARrest Systems
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The OXY-VENT Study
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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.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Audiovisual feedback from smartphone based app in people with Cardiopulmonary Resuscitation and Basic Cardiac Life Support, run by Hanyang University at 1 site in South Korea.
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 3 inclusion and 5 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: finished, as of the sponsor's last update on 27 Aug 2014. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in South Korea. Whether a site is taking part right now should be confirmed with that site. See every site.
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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Chest compression depth (time frame: within the first 30 days after the end of recording). The study lists 2 primary outcomes in all. 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 27 Aug 2014.