Cardio Respiratory ArrestSmartwatchNCT03828305
Effectiveness of a Network of Trained Volunteers Automatically Activated, on the Reduction of the Start Time of Cardiopulmonary Resuscitation Maneuvers. Study Protocol.
A study testing Training and creation of the Network-CPR in people with Cardio Respiratory Arrest, run by Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina.
Trial summary
Background Cardiorespiratory arrest (CRA) is a health emergency with high mortality. Mortality could depends on the start time of cardiopulmonary resuscitation (CPR) maneuvers (and the quality of its performance) and the use of the automated external defibrillator (AED). Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Cardio Respiratory Arrest
- What is being tested?
- Training and creation of the Network-CPR
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 475 participants
- Where
- No sites listed yet
- Study dates
- 1 Jun 2016to 31 Dec 2019
- 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
- Qualification of suitable, based on the evaluation of the competences during the course.
- Being over 18 years.
- Have an smartphone with Android operating system.
- The signing of the informed consent document
- The installation of the App on the smartphone.
Who cannot join
- Qualification of no-suitable, based on the evaluation of the competences during the course.
- No-being over 18 years.
- Have an smatphone with an operating system diferent from Android.
- no-singning of the informed consent document.
- The no-intallation of the App on the smartphone.
- No understood the language.
About this study
Background Cardiorespiratory arrest (CRA) is a health emergency with high mortality. Mortality could depends on the start time of cardiopulmonary resuscitation (CPR) maneuvers (and the quality of its performance) and the use of the automated external defibrillator (AED).
Methods / design The aim of the study is to determine the effectiveness of a network of volunteers automatically activated by smartwatch and smartphone, on the reduction of the start time of cardiopulmonary resuscitation maneuvers. It is developed in four phases: 1) validation of an application (App) for smartwatch developed to automatically generate a health alert in case of out-of-hospital cardiorespiratory arrest (OHCA); 2) training course in basic CPR maneuvers and use of the AED aimed at the civilian population; 3) creation of a network of volunteers trained in CPR and using the AED that covers the city; 4) simulation study in which members of the network of volunteers will be activated automatically through their smartphone to attend simulated OHCA. 134 activations of the alert will be made. On 67 occasions the alert will be directed to the emergency health services and to the network of volunteers (intervention group). On 67 occasions the alert will be directed to the emergency health services (control group). The arrival time of the first rescuer, category of the first rescuer (emergency services or network of volunteers), start time of the maneuvers and competence in the performance of the maneuvers will be recorded.
Discussion Training in CPR maneuvers is recommended for the civilian population and especially for relatives and close persons of people with heart disease to reduce the start time of CPR and improve survival rates due to CRA. This study aims to observe that the start time of CPR maneuvers and use of the AED will be lower in the intervention group than in the control group.
Read the detailed description
Methods/design Study aim This clinical trial aims to determine the effectiveness of a network of volunteers trained in CPR maneuvers and using the AED connected through an application (App) for smartwatch, which allows automatic activation in case of out-of-hospital cardiorespiratory arrest (OHCA), on the start time of the CPR maneuvers and use of the AED.
This study will be carried out in 4 phases. 1) validate an App for smartwatch that allows the automatic activation of a network of volunteers trained in CPR maneuvers and use of the AED (Network-CPR) and the emergency services, in case the user of the smartwatch suffers a OHCA; 2) training in basic CPR and use of the AED in the general population; 3) creating a network of volunteers from the subjects trained (Network-CPR); 4) determine the effectiveness of the automatic activation of the Network-CPR through an app for smartwatch on the start time of the CPR maneuvers and use of the AED; and to evaluate the competences in the performance of the maneuvers by the members of the Network-CPR through simulations in the city streets.
Development of the mobile app An App was developed in the Android operating system for smartwatch, an App for mobile smartphones with Android operating systems, and a platform to install in the central computer of the Primary Care Emergency Center (PCEC). In case of detecting an absence of the heart rate (>3 seconds without heartbeat) and falling down to the ground of the smartwatch carrier, the application will send an alert in the first place to the smartwatch, if it is a false positive the smartwatch carrier will deactivate it. If it is a real alert and after 6 seconds the smartwatch carrier does not deactivate it, a warning alert will be generated and sent automatically to an App installed on the smartphones of the members of the Network-CPR (limited to members that are within a radius of 300 meters where the warning alert was generated), and at the same time will also reach a platform installed in the central computer of the PCEC. The members of the Network-CPR will receive on their smartphone the signal with the geolocation of the CRA, the map with the fastest route to reach the location of the CRA and the point where the nearest AED is located.
Phase 1. Validation of the App. This validation will be done through the determination of automatic activations in various locations in the city, it will be determined if the alert reach the members of the Network-CPR and the PCEC and if it is geolocated in a precise way . In addition, during 3 months, four volunteers with high risk of CRA will carry the smartwatch and it will be determined if false activations (false positives) occur during this period of time.
Phase 2 and 3. Training and creation of the Network-CPR that will cover the city. This network will be created with certain population groups that are routinely in contact with susceptible persons of OHCA (police, firemen, teaching staff, health personnel, merchants, pharmacists, university students, gym monitors, etc.), in addition, relatives of people with heart disease will be included. In the case of elderly people who are alone, they will include their neighbors or caregivers. In the city, there are 2,105 people with heart disease susceptible to OHCA. The research team and the health personnel of the participating primary care centers (PCC) will offer training courses on basic CPR maneuvers and use of the AED, following the protocol of the Center Català de Ressucitació (CCR) [14]. The training is aimed at training 430 people (20% of the relatives of people with heart disease) and will be made by trainers accredited by the CCR. There will be a total of 30 sessions with groups of approximately 15 people.
At the end of the training courses, the research team will explain the project and offer voluntary participation in the Network-CPR. Recruitment of 100 participants (25% of the trained participants) is expected. This participation implies having a qualification of suitable, based on the evaluation of the competences during the course; being over 18 years; have a smartphone with Android operating system; the signing of the informed consent document; and the installation of the App receiving the alerts on the smartphone.
Phase 4. Simulation study. A total of 134 simulations will be carried out with simulated CRA warnings alerts in the city. On 67 times, the alerts will reach the Network-CPR and the emergency services (intervention group) and 67 times only the emergency services(control group).
The warnings alerts will be generated in 134 locations randomly, based on the locations where a CRA was notified to the emergency services during the year 2017 (51 locations). The intervention group will be activated through generated alerts that will arrive through the App for smartphones of the members of the Network-CPR that are in a radius of 300 meters; and through the platform installed in the PCEC central computer to the emergency services. The control group will be activated by telephone calls to the PCEC.
The simulations will be carried out during two periods (morning and afternoon). During the time of the simulations a medical doctor and an emergency nurse (PCEC team) will be in the PCEC, to be activated, go to the locations and perform the simulations. The PCEC team will not know in which simulations they are activated or in which the Network-CPR is activated.
At the locations you will find two trained and standardized health personnel (victim team: medical doctor or an emergency nurse and a trainer accredited by the CCR), duly identified, with a CPR mannequin and a practice AED.
- Conditions
- Cardio Respiratory Arrest
- Being tested
- Training and creation of the Network-CPR, Control Group
- Keywords
- Out of hospital cardiac arrest, cardiopulmonary resuscitation, automated external defibrillators, emergency medical system services, mobile phone, Primary healt-care, Technology
- Medical subject headings
- Heart Arrest, Out-of-Hospital Cardiac Arrest
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Training and creation of the Network-CPROther
Training and creation of the Network-CPR that will cover the city. This network will be created with certain population groups that are routinely in contact with susceptible persons of OHCA (police, firemen, teaching staff, health personnel, merchants, pharmacists, university students, etc.), in addition, relatives of people with heart disease will be included. In the case of elderly people who are alone, they will include their neighbors or caregivers. In the city, there are 2,105 people with heart disease susceptible to OHCA. The research team and the health personnel of the participating primary care centers (PCC) will offer training courses on basic CPR maneuvers and use of the AED, following the protocol of the Center Català de Ressucitació (CCR). The training is aimed at training 430 people (20% of the relatives of people with heart disease) and will be made by trainers accredited by the CCR. There will be a total of 30 sessions with groups of approximately 15 people.
Control GroupOther
No intervention
| Study group | Role | What they receive |
|---|---|---|
| Training and creation of the Network-CPR | Experimental | Training in CPR Receives: Other: Training and creation of the Network-CPR |
| Control Group | Active comparator | Primary Care Center Emergency Personnel Receives: Other: Control Group |
What is being measured
The primary outcome is the main question the study is designed to answer.
Start time of the maneuvers (Tim)
time (minutes and seconds) elapsed between the start of the simulated CRA (T0) and the start of the CPR maneuvers (T2b or T3b in case of arrival of PCEC team or Network-CPR , respectively). It is considered that the maneuvers stars when the chest compressions are started in the manikin.
Measured: 6 months
Time of start of the use of the AED (Tid)
time elapsed between the start of the simulated CRA (T0) and the start of the use of the AED (T2d or T3d in case of arrival of the PCEC team or Netwrok-CPR, respectively) . It is considered that the use of the AED starts when the patches are placed on the thorax of the manikin.
Measured: 6 months
Response time of the PCCE team (Trc)
time between the start of the simulated CRA (T0) and the arrival of the PCEC team (T2).
Measured: 6 months
Response time of the Network-CPR (Trr)
time between the start of the simulated CRA (T0) and the arrival of the Network-CPR (T3).
Measured: 6 months
AED arrival time (TllD)
Time elapsed between the start of the simulated CRA (T0) and the arrival of the AED (T2c or T3c, in case of arrival of PCEC team or Network-CPR, respectively). It is necessary to register who brings the AED, members of the Network-CPR, personnel of the PCEC team or an external person to whom assistance has been requested.
Measured: 6 months
Secondary outcomes (1)
Evaluation of the competence of the members of the Network-CPR
Item score: 1p per item. a) safe approach; b) evaluation of the state of consciousness; c) opening of the airway; d) spontaneous breathing check; e) ask for help; f) chest compressions (quality); g) frequency of comprehensions; h) two insufflations (quality); i) alternation compressions/insufflations. It will be considered that you have performed a correct CPR maneuver if 8 of the 9 items evaluated are performed correctly
Measured: 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Feb 2019
- Study start1 Jun 2016
- Primary completion1 Jun 2016
- Study completion31 Dec 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Cardio Respiratory ArrestStudies 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
- Health services research
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Model description
- This clinical trial aims to determine the effectiveness of a network of volunteers trained in CPR maneuvers and using the AED connected through an application (App) for smartwatch, which allows automatic activation in case of out-of-hospital cardiorespiratory arrest (OHCA), on the start time of the CPR maneuvers and use of the AED.
- Masking
- None (open label)
- Enrolment
- 475 participants (actual)
Sponsor and investigators
- Lead sponsor
- Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
- Sponsor type
- University, hospital or other
- Collaborators
- Department of Health, Generalitat de Catalunya
- Responsible party
- Sponsor
- Investigators
- Cristina Rey-Reñones, Phd, Principal investigator, Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03828305
- Sponsor's protocol ID
- P17/075
- Acronym
- Smartwatch
- Status last verified
- Jul 2020
- First submitted
- 1 Feb 2019
- Last updated
- 29 Jul 2020
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Publications
Del Pozo A, Villalobos F, Rey-Renones C, Granado E, Sabate D, Poblet C, Calvet A, Basora J, Castro A, Flores G. Effectiveness of a network of automatically activated trained volunteers on the reduction of cardiopulmonary resuscitation manoueuvers initiation time: study protocol. BMC Public Health. 2019 May 14;19(1):572. doi: 10.1186/s12889-019-6896-9.
PubMed 31088520
Study at a glance
From the registry record, last updated by the sponsor on 29 Jul 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effectiveness of a Network of Trained Volunteers Automatically Activated, on the Reduction of the Start Time of Cardiopulmonary Resuscitation Maneuvers. Study Protocol.
- ClinicalTrials.gov ID
- NCT03828305
- Acronym / sponsor ID
- Smartwatch / P17/075
- Conditions
- Cardio Respiratory Arrest
- Keywords
- Out of hospital cardiac arrest, cardiopulmonary resuscitation, automated external defibrillators, emergency medical system services, mobile phone, Primary healt-care, Technology
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 475 participants (actual)
- Lead sponsor
- Fundacio d'Investigacio en Atencio Primaria Jordi Gol i GurinaUniversity, hospital or other
- Collaborators
- Department of Health, Generalitat de Catalunya
- Study start
- 1 Jun 2016 (actual)
- Primary completion
- 1 Jun 2016 (actual)
- Study completion
- 31 Dec 2019 (actual)
- First posted
- 4 Feb 2019 (actual)
- 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.
Background Cardiorespiratory arrest (CRA) is a health emergency with high mortality. Mortality could depends on the start time of cardiopulmonary resuscitation (CPR) maneuvers (and the quality of its performance) and the use of the automated external defibrillator (AED).
Methods / design The aim of the study is to determine the effectiveness of a network of volunteers automatically activated by smartwatch and smartphone, on the reduction of the start time of cardiopulmonary resuscitation maneuvers. It is developed in four phases: 1) validation of an application (App) for smartwatch developed to automatically generate a health alert in case of out-of-hospital cardiorespiratory arrest (OHCA); 2) training course in basic CPR maneuvers and use of the AED aimed at the civilian population; 3) creation of a network of volunteers trained in CPR and using the AED that covers the city; 4) simulation study in which members of the network of volunteers will be activated automatically through their smartphone to attend simulated OHCA. 134 activations of the alert will be made. On 67 occasions the alert will be directed to the emergency health services and to the network of volunteers (intervention group). On 67 occasions the alert will be directed to the emergency health services (control group). The arrival time of the first rescuer, category of the first rescuer (emergency services or network of volunteers), start time of the maneuvers and competence in the performance of the maneuvers will be recorded.
Discussion Training in CPR maneuvers is recommended for the civilian population and especially for relatives and close persons of people with heart disease to reduce the start time of CPR and improve survival rates due to CRA. This study aims to observe that the start time of CPR maneuvers and use of the AED will be lower in the intervention group than in the control group.
Detailed description
Methods/design Study aim This clinical trial aims to determine the effectiveness of a network of volunteers trained in CPR maneuvers and using the AED connected through an application (App) for smartwatch, which allows automatic activation in case of out-of-hospital cardiorespiratory arrest (OHCA), on the start time of the CPR maneuvers and use of the AED.
This study will be carried out in 4 phases. 1) validate an App for smartwatch that allows the automatic activation of a network of volunteers trained in CPR maneuvers and use of the AED (Network-CPR) and the emergency services, in case the user of the smartwatch suffers a OHCA; 2) training in basic CPR and use of the AED in the general population; 3) creating a network of volunteers from the subjects trained (Network-CPR); 4) determine the effectiveness of the automatic activation of the Network-CPR through an app for smartwatch on the start time of the CPR maneuvers and use of the AED; and to evaluate the competences in the performance of the maneuvers by the members of the Network-CPR through simulations in the city streets.
Development of the mobile app An App was developed in the Android operating system for smartwatch, an App for mobile smartphones with Android operating systems, and a platform to install in the central computer of the Primary Care Emergency Center (PCEC). In case of detecting an absence of the heart rate (>3 seconds without heartbeat) and falling down to the ground of the smartwatch carrier, the application will send an alert in the first place to the smartwatch, if it is a false positive the smartwatch carrier will deactivate it. If it is a real alert and after 6 seconds the smartwatch carrier does not deactivate it, a warning alert will be generated and sent automatically to an App installed on the smartphones of the members of the Network-CPR (limited to members that are within a radius of 300 meters where the warning alert was generated), and at the same time will also reach a platform installed in the central computer of the PCEC. The members of the Network-CPR will receive on their smartphone the signal with the geolocation of the CRA, the map with the fastest route to reach the location of the CRA and the point where the nearest AED is located.
Phase 1. Validation of the App. This validation will be done through the determination of automatic activations in various locations in the city, it will be determined if the alert reach the members of the Network-CPR and the PCEC and if it is geolocated in a precise way . In addition, during 3 months, four volunteers with high risk of CRA will carry the smartwatch and it will be determined if false activations (false positives) occur during this period of time.
Phase 2 and 3. Training and creation of the Network-CPR that will cover the city. This network will be created with certain population groups that are routinely in contact with susceptible persons of OHCA (police, firemen, teaching staff, health personnel, merchants, pharmacists, university students, gym monitors, etc.), in addition, relatives of people with heart disease will be included. In the case of elderly people who are alone, they will include their neighbors or caregivers. In the city, there are 2,105 people with heart disease susceptible to OHCA. The research team and the health personnel of the participating primary care centers (PCC) will offer training courses on basic CPR maneuvers and use of the AED, following the protocol of the Center Català de Ressucitació (CCR) [14]. The training is aimed at training 430 people (20% of the relatives of people with heart disease) and will be made by trainers accredited by the CCR. There will be a total of 30 sessions with groups of approximately 15 people.
At the end of the training courses, the research team will explain the project and offer voluntary participation in the Network-CPR. Recruitment of 100 participants (25% of the trained participants) is expected. This participation implies having a qualification of suitable, based on the evaluation of the competences during the course; being over 18 years; have a smartphone with Android operating system; the signing of the informed consent document; and the installation of the App receiving the alerts on the smartphone.
Phase 4. Simulation study. A total of 134 simulations will be carried out with simulated CRA warnings alerts in the city. On 67 times, the alerts will reach the Network-CPR and the emergency services (intervention group) and 67 times only the emergency services(control group).
The warnings alerts will be generated in 134 locations randomly, based on the locations where a CRA was notified to the emergency services during the year 2017 (51 locations). The intervention group will be activated through generated alerts that will arrive through the App for smartphones of the members of the Network-CPR that are in a radius of 300 meters; and through the platform installed in the PCEC central computer to the emergency services. The control group will be activated by telephone calls to the PCEC.
The simulations will be carried out during two periods (morning and afternoon). During the time of the simulations a medical doctor and an emergency nurse (PCEC team) will be in the PCEC, to be activated, go to the locations and perform the simulations. The PCEC team will not know in which simulations they are activated or in which the Network-CPR is activated.
At the locations you will find two trained and standardized health personnel (victim team: medical doctor or an emergency nurse and a trainer accredited by the CCR), duly identified, with a CPR mannequin and a practice AED.
Study design
- Primary purpose
- Health services research
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- This clinical trial aims to determine the effectiveness of a network of volunteers trained in CPR maneuvers and using the AED connected through an application (App) for smartwatch, which allows automatic activation in case of out-of-hospital cardiorespiratory arrest (OHCA), on the start time of the CPR maneuvers and use of the AED.
| Arm | Type | Receives |
|---|---|---|
| Training and creation of the Network-CPR | Experimental | Other: Training and creation of the Network-CPRTraining in CPR |
| Control Group | Active comparator | Other: Control GroupPrimary Care Center Emergency Personnel |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Qualification of suitable, based on the evaluation of the competences during the course.
- Being over 18 years.
- Have an smartphone with Android operating system.
- The signing of the informed consent document
- The installation of the App on the smartphone.
Key exclusion criteria (6 listed)
- Qualification of no-suitable, based on the evaluation of the competences during the course.
- No-being over 18 years.
- Have an smatphone with an operating system diferent from Android.
- no-singning of the informed consent document.
- The no-intallation of the App on the smartphone.
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 |
|---|---|---|
| Training and creation of the Network-CPRTraining and creation of the Network-CPR that will cover the city. This network will be created with certain population groups that are routinely in contact with susceptible persons of OHCA (police, firemen, teaching staff, health personnel, merchants, pharmacists, university students, etc.), in addition, relatives of people with heart disease will be included. In the case of elderly people who are alone, they will include their neighbors or caregivers. In the city, there are 2,105 people with heart disease susceptible to OHCA. The research team and the health personnel of the participating primary care centers (PCC) will offer training courses on basic CPR maneuvers and use of the AED, following the protocol of the Center Català de Ressucitació (CCR). The training is aimed at training 430 people (20% of the relatives of people with heart disease) and will be made by trainers accredited by the CCR. There will be a total of 30 sessions with groups of approximately 15 people. | Other | Training and creation of the Network-CPR |
| Control GroupNo intervention | Other | Control Group |
Primary outcome
Start time of the maneuvers (Tim)
Time frame: 6 months
time (minutes and seconds) elapsed between the start of the simulated CRA (T0) and the start of the CPR maneuvers (T2b or T3b in case of arrival of PCEC team or Network-CPR , respectively). It is considered that the maneuvers stars when the chest compressions are started in the manikin.
Time of start of the use of the AED (Tid)
Time frame: 6 months
time elapsed between the start of the simulated CRA (T0) and the start of the use of the AED (T2d or T3d in case of arrival of the PCEC team or Netwrok-CPR, respectively) . It is considered that the use of the AED starts when the patches are placed on the thorax of the manikin.
Response time of the PCCE team (Trc)
Time frame: 6 months
time between the start of the simulated CRA (T0) and the arrival of the PCEC team (T2).
Response time of the Network-CPR (Trr)
Time frame: 6 months
time between the start of the simulated CRA (T0) and the arrival of the Network-CPR (T3).
AED arrival time (TllD)
Time frame: 6 months
Time elapsed between the start of the simulated CRA (T0) and the arrival of the AED (T2c or T3c, in case of arrival of PCEC team or Network-CPR, respectively). It is necessary to register who brings the AED, members of the Network-CPR, personnel of the PCEC team or an external person to whom assistance has been requested.
1 secondary outcome
Evaluation of the competence of the members of the Network-CPR
Time frame: 6 months
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 29 Jul 2020.
- Derived from this study: PubMed 31088520Del Pozo A, Villalobos F, Rey-Renones C, Granado E, Sabate D, Poblet C, Calvet A, Basora J, Castro A, Flores G. Effectiveness of a network of automatically activated trained volunteers on the reduction of cardiopulmonary resuscitation manoueuvers initiation time: study protocol. BMC Public Health. 2019 May 14;19(1):572. doi: 10.1186/s12889-019-6896-9.
- Individual participant dataSharing planned: Undecided
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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.
Cristina Rey-Reñones, Phd principal investigator
Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
Questions about this trial
What is this clinical trial studying?
A study testing Training and creation of the Network-CPR in people with Cardio Respiratory Arrest, run by Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina.
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 5 inclusion and 6 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 29 Jul 2020. 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?
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?
Start time of the maneuvers (Tim) (time frame: 6 months). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03828305, which also lists 1 linked publication.
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 29 Jul 2020; AzTrials last refreshed its copy on 7 Nov 2026.