ECG Electrode Site ReactionWECGNCT04786509
Wireless ECG Body Sensor During Field Testing
An observational study of ECG Electrode Site Reaction, run by University of Belgrade at 1 site in Serbia.
Trial summary
Wireless body ECG sensor is a feasible solution for reliable and accurate long-term heart rhythm monitoring. However, there were no studies that delt with usability of this sensor in field testing. Read more about this study
- Who is it for?
- Ages 20 to 25 years, men onlyHealthy volunteers can take part
- Conditions the study is for
- ECG Electrode Site Reaction
- What is being tested?
- Field tests
- How many people
- 23 participants
- Where
- 1 siteSerbia
- Study dates
- 1 Jun 2018to 1 Aug 2018
- Phase
- Observational
- 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 20 to 25 years
- Men only
- Healthy volunteers accepted
- Adult
Study population: Twenty-three were included, 13 males and 10 females, age between 19 and 23 years (Age = 20.56±1.19 years; Body height = 177.28±9.76 cm; Body mass = 70.11±7.68 kg). All participants were physically active non-athletes, with daily involvement (3-5 times per week, 30 to 60 minutes of moderate to high intensity) in various physical activities (team sports, cyclic activities, resistance training). To meet the criteria for participation in the study, participants had to confirm they were healthy, and without known previous cardiac problems.
Who may be able to join
- Physically active participants
Who cannot join
- Heart diseases
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Usability of Wireless ECG Body Sensor for Cardiac Function Monitoring During Field Testing
Wireless body ECG sensor is a feasible solution for reliable and accurate long-term heart rhythm monitoring. However, there were no studies that delt with usability of this sensor in field testing. Accordingly, the aim of the study is to evaluate the quality of ECG signal measured with wearable wireless ECG body-sensor when used in field test settings and to determine how different types of sensors' fixation affect quality of the ECG signal during submaximal and maximal running settings. Twenty-three participants, 10 females and 13 males, were included in the study (20.56±1.19 years). All subjects performed shuttle run (SR), Cooper 2400 m (C), and 100 m sprint test (S), once wearing the sensor attached to self-adhesive skin electrodes, additionally fixed with self-adhesive tapes, and secondly with the sensor attached to Polar belt and strapped around the chests. Test outcomes were compared applying Student t-test for dependent variables, or non-parametric Wilcoxon test, depending on the results of normality test.
Read the detailed description
Today's lifestyle presents high risk for cardiovascular diseases, which is a leading cause of death worldwide. Previous studies have targeted various risk factors for development of cardiovascular diseases, such as high blood pressure, smoking, type 2 diabetes, obesity, psychological stress and physical inactivity.
Increased level of physical activity has numerous beneficial long-term effects on cardiovascular system, and might decrease relative risk of sudden cardiac death. However, the risk of unexpected cardiovascular events is increased during, and immediately after intense exercise. Two studies conducted in France, reported a daily incidence of three sudden deaths and four myocardial infarctions during regular physical activity in the general population. Twelve-year longitudinal study showed that average age of young recreational athletes in Switzerland who died during physical activity was 27.6 years, with the incidence of 0.52/100.000 per year. Some studies reported dramatic increase of unexpected cardiovascular events in a middle age group of recreational population, which was at the level of 6.5/100.000 per year. Furthermore, several studies reported higher incidence of sports related cardiovascular events between general population in comparison with professional athletes. Males are more affected, and the most affected age group is middle-aged between 35 and 59 years.
Previous studies noticed that the key challenge is identification of structural heart disease and inheritable conditions that increase incidence for lethal arrhythmias during exercise, because sudden cardiac events often occurs without any warning or prediction. Therefore, early detection of persons with higher risk for sudden cardiac death is of crucial importance. In this regard, numerous European countries have introduced a mandatory medical examination for all persons registered in sports clubs or associations. Exercise stress test (EST) which includes electrocardiographic (ECG) monitoring is an important part of examination. However, the problem arises from the fact that EST is especially sensitive for testing individuals with previous known symptoms of cardiac disease, while the positive predictive value of an EST in asymptomatic subjects is relatively low. On the other hand, it was proven that long term ECG monitoring during regular daily activities can be very useful in detection of heart disease in people who had normal 12-lead ECG, and negative Master two-step tests. Also, it was proven that it is possible to detect atrial fibrillation in asymptomatic people with long-term one-channel ECG monitoring.
Recent studies showed that the wireless body ECG sensor is a feasible solution for reliable and accurate long-term heart rhythm monitoring, but the sensor placement and fixation is an important factor which can influence the signal quality and needs to be taken into consideration. In accordance with previously said, our main goal was to determine whether it is possible to measure quality electrocardiographic report using ECG body-sensor during standardized outdoor tests. Additional aim was to determine whether different types of sensors' fixation affect quality of the ECG signal during submaximal and maximal running settings.
Twenty-three were included, 13 males and 10 females, age between 19 and 23 years (Age = 20.56±1.19 years; Body height = 177.28±9.76 cm; Body mass = 70.11±7.68 kg). All participants were physically active non-athletes, with daily involvement (3-5 times per week, 30 to 60 minutes of moderate to high intensity) in various physical activities (team sports, cyclic activities, resistance training). To meet the criteria for participation in the study, participants had to confirm they were healthy, and without known previous cardiac problems. In accordance with the Declaration of Helsinki participants gave the signed consent for participation in the study. Prior to the tests, the purpose and protocols of the study were explained in details to each participant. Ethics approval for the study was obtained from the Institutional Ethical committee (Approval no. 02-1359/18-2).
ECG Signal Monitoring Wireless ECG body-sensor Savvy (Saving d.o.o., Ljubljana, Slovenia), which is a certified medical device, was used for collecting ECG data. The body-sensor allows ECG measurements during long-term exercise, with a sampling rate between 125 Hz and 1000 Hz. An Android application, MobECG, which runs on a smartphone, connected to the sensor via Bluetooth, captures and displays the measured data and saves it in the smartphone memory for further processing.
The optimal placement for the electrodes was close to the heart in order to obtain the appropriate amplitude of ECG signal. Considering that the signals from the electrical muscular activity (EMG) could disturb the ECG signal, especially during physical activity, sensor position was placed to avoid large muscle groups. In this study, we tested position marked as left inferior (LI). At the LI position electrodes were placed at the positions of standard anterior precordial leads V1 and V2, and then sensor was translated downward by approximately 10 cm (below the xiphoid), where the influence of muscular disturbances is expected to be minimal.
In the first test standard self-adhesive Skintact ECG electrodes type PREMIER T-60 were used (Leonhard Lang GmbH, Innsbruck, Austria). The electrodes were in the original packaging and used according to the manufacturer's instructions. The ECG electrodes were positioned 5 cm apart. Before the positioning, the skin of the subjects was cleaned with diluted ethanol. Then, two electrodes were stuck at the LI position, and the ECG body-sensor was connected. Sensor was additionally fixed with self-adhesive Omniplast 2.5 cm tape (Paul Hartmann AG, Heidenheim, Germany), specially designed to fix Holter electrodes (see Figure 1). Both parts of the sensor were fixed together with one, approximately 40-cm-long strip of tape. In the second measurement Polar soft strap belt (Polar Electro Oy, Finland) was used to connect the sensor.
The measured ECG data were continuously stored in the smartphone memory and transferred after the completion of the measurements to a personal computer. All the ECG measurements were analysed retrospectively. The subsequent ECG analyses and signal quality were made with medically certified Holter interpretation software QuickReader®AFT-1000 (Holter Supplies, Paris, France). Moreover, all the measurements and the results were visually examined by a medical doctor. Only signals where QRS waves were clear and recognized without doubt where marked as useful. Variables used in study were: Detected QRS, QRS detected as negative (%), False negative detection (%), Correct software detection (%), Load / speed with still assessable HR (%), Maximal HR [bpm], Average running time (s) (for Cooper 2400 and 100 m tests) and Average achieved intensity (for Shutlle run).
In this study we used three different standardized running tests, one sub-maximal test - Cooper 2400 m (C), and two maximal (all-out) tests - 100 m sprint (S) and shuttle run (SR). In C test participants had to run 2400 m, while in S test they had to run 100 m at the highest possible speed. In SR test standard test protocol was used. Participants had to run 20 meters and step across the line before audio sign (beep). Test started with speed of 8.5 km/h which was increased 0.5 km/h every minute, until exhaustion. Test was finished when subject couldn't reach the line two times in a row, before audio sign.
Every participant made six tests, two C, S and SR tests. All tests were made in the morning, and participant performed one test per day and retest until next day. Break between two tests was at least 24 hours. Before performing the tests, the electrodes and sensor were positioned at the LI position, and the participants sat down for 5 minutes, while the ECG was recording. When the test was finished the participant sat down and rest for next 5 minutes without interrupting the ECG recording.
Descriptive statistics were calculated for all measured variables, and test of normality was made for all the data. For the data which was not distributed normally by Kolmogorov-Smirnov and Shapiro-Wilk test results, based on the results of Skewness, transformation with function Log10 or Log10 reflexion was made. For all original and transformed variables that showed normal distribution, for determination of differences student t-test for dependent variables was used, while non-parametric Wilcoxon test was used for those which were not distributed normally. Intra-class correlation was counted for repeated measurements. The significance level was set to p < 0.05. The statistical analysis was conducted using IBM SPSS Statistics 20 software.
- Conditions
- ECG Electrode Site Reaction
- Being tested
- Field tests
- Keywords
- telemetry, exercise testing, prevention, ECG, field tests
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Field testsDiagnostic test
In this study we used three different standardized running tests, one sub-maximal test - Cooper 2400 m (C), and two maximal (all-out) tests - 100 m sprint (S) and shuttle run (SR).
| Study group | Role | What they receive |
|---|---|---|
| ECG sensor | All subjects performed shuttle run (SR), Cooper 2400 m (C), and 100 m sprint test (S), once wearing the sensor attached to self-adhesive skin electrodes, additionally fixed with self-adhesive tapes, and secondly with the sensor attached to Polar belt and strapped around the chests. Receives: Diagnostic Test: Field tests |
What is being measured
The primary outcome is the main question the study is designed to answer.
Detected QRS
Number of detected QRS during field tests
Measured: 10 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Mar 2021
- Study start1 Jun 2018
- Primary completion1 Jul 2018
- Study completion1 Aug 2018
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for ECG Electrode Site ReactionStudies 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
- Observational
- Observational model
- Other
- Time perspective
- Cross-sectional
- Enrolment
- 23 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Belgrade
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Vladimir Ilic, University of Belgrade
- Investigators
- Vladimir Ilić, PhD, Principal investigator, Faculty of Sport and Physical Education, University of Belgrade
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04786509
- Sponsor's protocol ID
- 02-1359/18-2
- Acronym
- WECG
- Status last verified
- Mar 2021
- First submitted
- 3 Mar 2021
- Last updated
- 10 Mar 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 10 Mar 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Usability of Wireless ECG Body Sensor for Cardiac Function Monitoring During Field Testing
- ClinicalTrials.gov ID
- NCT04786509
- Acronym / sponsor ID
- WECG / 02-1359/18-2
- Conditions
- ECG Electrode Site Reaction
- Keywords
- telemetry, exercise testing, prevention, ECG, field tests
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 23 participants (actual)
- Lead sponsor
- University of BelgradeUniversity, hospital or other
- Study start
- 1 Jun 2018 (actual)
- Primary completion
- 1 Jul 2018 (actual)
- Study completion
- 1 Aug 2018 (actual)
- First posted
- 8 Mar 2021 (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.
Wireless body ECG sensor is a feasible solution for reliable and accurate long-term heart rhythm monitoring. However, there were no studies that delt with usability of this sensor in field testing. Accordingly, the aim of the study is to evaluate the quality of ECG signal measured with wearable wireless ECG body-sensor when used in field test settings and to determine how different types of sensors' fixation affect quality of the ECG signal during submaximal and maximal running settings. Twenty-three participants, 10 females and 13 males, were included in the study (20.56±1.19 years). All subjects performed shuttle run (SR), Cooper 2400 m (C), and 100 m sprint test (S), once wearing the sensor attached to self-adhesive skin electrodes, additionally fixed with self-adhesive tapes, and secondly with the sensor attached to Polar belt and strapped around the chests. Test outcomes were compared applying Student t-test for dependent variables, or non-parametric Wilcoxon test, depending on the results of normality test.
Detailed description
Today's lifestyle presents high risk for cardiovascular diseases, which is a leading cause of death worldwide. Previous studies have targeted various risk factors for development of cardiovascular diseases, such as high blood pressure, smoking, type 2 diabetes, obesity, psychological stress and physical inactivity.
Increased level of physical activity has numerous beneficial long-term effects on cardiovascular system, and might decrease relative risk of sudden cardiac death. However, the risk of unexpected cardiovascular events is increased during, and immediately after intense exercise. Two studies conducted in France, reported a daily incidence of three sudden deaths and four myocardial infarctions during regular physical activity in the general population. Twelve-year longitudinal study showed that average age of young recreational athletes in Switzerland who died during physical activity was 27.6 years, with the incidence of 0.52/100.000 per year. Some studies reported dramatic increase of unexpected cardiovascular events in a middle age group of recreational population, which was at the level of 6.5/100.000 per year. Furthermore, several studies reported higher incidence of sports related cardiovascular events between general population in comparison with professional athletes. Males are more affected, and the most affected age group is middle-aged between 35 and 59 years.
Previous studies noticed that the key challenge is identification of structural heart disease and inheritable conditions that increase incidence for lethal arrhythmias during exercise, because sudden cardiac events often occurs without any warning or prediction. Therefore, early detection of persons with higher risk for sudden cardiac death is of crucial importance. In this regard, numerous European countries have introduced a mandatory medical examination for all persons registered in sports clubs or associations. Exercise stress test (EST) which includes electrocardiographic (ECG) monitoring is an important part of examination. However, the problem arises from the fact that EST is especially sensitive for testing individuals with previous known symptoms of cardiac disease, while the positive predictive value of an EST in asymptomatic subjects is relatively low. On the other hand, it was proven that long term ECG monitoring during regular daily activities can be very useful in detection of heart disease in people who had normal 12-lead ECG, and negative Master two-step tests. Also, it was proven that it is possible to detect atrial fibrillation in asymptomatic people with long-term one-channel ECG monitoring.
Recent studies showed that the wireless body ECG sensor is a feasible solution for reliable and accurate long-term heart rhythm monitoring, but the sensor placement and fixation is an important factor which can influence the signal quality and needs to be taken into consideration. In accordance with previously said, our main goal was to determine whether it is possible to measure quality electrocardiographic report using ECG body-sensor during standardized outdoor tests. Additional aim was to determine whether different types of sensors' fixation affect quality of the ECG signal during submaximal and maximal running settings.
Twenty-three were included, 13 males and 10 females, age between 19 and 23 years (Age = 20.56±1.19 years; Body height = 177.28±9.76 cm; Body mass = 70.11±7.68 kg). All participants were physically active non-athletes, with daily involvement (3-5 times per week, 30 to 60 minutes of moderate to high intensity) in various physical activities (team sports, cyclic activities, resistance training). To meet the criteria for participation in the study, participants had to confirm they were healthy, and without known previous cardiac problems. In accordance with the Declaration of Helsinki participants gave the signed consent for participation in the study. Prior to the tests, the purpose and protocols of the study were explained in details to each participant. Ethics approval for the study was obtained from the Institutional Ethical committee (Approval no. 02-1359/18-2).
ECG Signal Monitoring Wireless ECG body-sensor Savvy (Saving d.o.o., Ljubljana, Slovenia), which is a certified medical device, was used for collecting ECG data. The body-sensor allows ECG measurements during long-term exercise, with a sampling rate between 125 Hz and 1000 Hz. An Android application, MobECG, which runs on a smartphone, connected to the sensor via Bluetooth, captures and displays the measured data and saves it in the smartphone memory for further processing.
The optimal placement for the electrodes was close to the heart in order to obtain the appropriate amplitude of ECG signal. Considering that the signals from the electrical muscular activity (EMG) could disturb the ECG signal, especially during physical activity, sensor position was placed to avoid large muscle groups. In this study, we tested position marked as left inferior (LI). At the LI position electrodes were placed at the positions of standard anterior precordial leads V1 and V2, and then sensor was translated downward by approximately 10 cm (below the xiphoid), where the influence of muscular disturbances is expected to be minimal.
In the first test standard self-adhesive Skintact ECG electrodes type PREMIER T-60 were used (Leonhard Lang GmbH, Innsbruck, Austria). The electrodes were in the original packaging and used according to the manufacturer's instructions. The ECG electrodes were positioned 5 cm apart. Before the positioning, the skin of the subjects was cleaned with diluted ethanol. Then, two electrodes were stuck at the LI position, and the ECG body-sensor was connected. Sensor was additionally fixed with self-adhesive Omniplast 2.5 cm tape (Paul Hartmann AG, Heidenheim, Germany), specially designed to fix Holter electrodes (see Figure 1). Both parts of the sensor were fixed together with one, approximately 40-cm-long strip of tape. In the second measurement Polar soft strap belt (Polar Electro Oy, Finland) was used to connect the sensor.
The measured ECG data were continuously stored in the smartphone memory and transferred after the completion of the measurements to a personal computer. All the ECG measurements were analysed retrospectively. The subsequent ECG analyses and signal quality were made with medically certified Holter interpretation software QuickReader®AFT-1000 (Holter Supplies, Paris, France). Moreover, all the measurements and the results were visually examined by a medical doctor. Only signals where QRS waves were clear and recognized without doubt where marked as useful. Variables used in study were: Detected QRS, QRS detected as negative (%), False negative detection (%), Correct software detection (%), Load / speed with still assessable HR (%), Maximal HR [bpm], Average running time (s) (for Cooper 2400 and 100 m tests) and Average achieved intensity (for Shutlle run).
In this study we used three different standardized running tests, one sub-maximal test - Cooper 2400 m (C), and two maximal (all-out) tests - 100 m sprint (S) and shuttle run (SR). In C test participants had to run 2400 m, while in S test they had to run 100 m at the highest possible speed. In SR test standard test protocol was used. Participants had to run 20 meters and step across the line before audio sign (beep). Test started with speed of 8.5 km/h which was increased 0.5 km/h every minute, until exhaustion. Test was finished when subject couldn't reach the line two times in a row, before audio sign.
Every participant made six tests, two C, S and SR tests. All tests were made in the morning, and participant performed one test per day and retest until next day. Break between two tests was at least 24 hours. Before performing the tests, the electrodes and sensor were positioned at the LI position, and the participants sat down for 5 minutes, while the ECG was recording. When the test was finished the participant sat down and rest for next 5 minutes without interrupting the ECG recording.
Descriptive statistics were calculated for all measured variables, and test of normality was made for all the data. For the data which was not distributed normally by Kolmogorov-Smirnov and Shapiro-Wilk test results, based on the results of Skewness, transformation with function Log10 or Log10 reflexion was made. For all original and transformed variables that showed normal distribution, for determination of differences student t-test for dependent variables was used, while non-parametric Wilcoxon test was used for those which were not distributed normally. Intra-class correlation was counted for repeated measurements. The significance level was set to p < 0.05. The statistical analysis was conducted using IBM SPSS Statistics 20 software.
Study design
- Observational model
- Other
- Time perspective
- Cross-sectional
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| ECG sensor | – | Diagnostic Test: Field testsAll subjects performed shuttle run (SR), Cooper 2400 m (C), and 100 m sprint test (S), once wearing the sensor attached to self-adhesive skin electrodes, additionally fixed with self-adhesive tapes, and secondly with the sensor attached to Polar belt and strapped around the chests. |
Who may qualify
- Ages
- 20 to 25 years
- Sex
- Male only
- Healthy volunteers
- Accepted
- Age groups
- Adult
- Study population
- Twenty-three were included, 13 males and 10 females, age between 19 and 23 years (Age = 20.56±1.19 years; Body height = 177.28±9.76 cm; Body mass = 70.11±7.68 kg). All participants were physically active non-athletes, with daily involvement (3-5 times per week, 30 to 60 minutes of moderate to high intensity) in various physical activities (team sports, cyclic activities, resistance training). To meet the criteria for participation in the study, participants had to confirm they were healthy, and without known previous cardiac problems.
Key inclusion criteria (1 listed)
- Physically active participants
Key exclusion criteria (1 listed)
- Heart diseases
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 |
|---|---|---|
| Field testsIn this study we used three different standardized running tests, one sub-maximal test - Cooper 2400 m (C), and two maximal (all-out) tests - 100 m sprint (S) and shuttle run (SR). | Diagnostic test | ECG sensor |
Primary outcome
Detected QRS
Time frame: 10 weeks
Number of detected QRS during field tests
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 10 Mar 2021.
- Individual participant dataSharing planned: No
Related trials for ECG Electrode Site Reaction
Recruiting
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Sudden Unexplained Infant Death, Apnea of Newborn
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.
Vladimir Ilić, PhD principal investigator
Faculty of Sport and Physical Education, University of Belgrade
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of ECG Electrode Site Reaction, run by University of Belgrade at 1 site in Serbia.
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: finished, as of the sponsor's last update on 10 Mar 2021. 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 Serbia. 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?
Detected QRS (time frame: 10 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 10 Mar 2021.