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20 protocols using polar s810i

1

IET and 3MT Performance in Hot and Neutral Environments

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In this study, all participants randomly performed the IETs under HT (ambient temperature, 35.4 ± 0.8 °C; humidity, 36.2 ± 4.7%RH) and NT (ambient temperature, 22.3 ± 0.6 °C; humidity, 39.3 ± 6.4%RH) in an environmental chamber, respectively. Participants underwent IETs under NT and HT in a randomised crossover design. Following completion of the IETs, 3MTs were also performed in a randomised crossover manner. Each participant underwent four tests separated by ≥48 h. Before the tests began, participants sat for 20-min under the same temperature before the exercise tests to acclimatise the different environmental conditions [17 (link)]. In addition, the participants weighed themselves before and after the experiment to record the dehydration conditions. During the measurement process, a portable gas analysis system (Cortex Metamax 3B, Cortex Biophysik, Leipzig, Germany) and a telemetry system with a wireless chest strap (Polar S810i; Polar Electro, Inc., Oy, Kempele, Finland) were used to collect oxygen uptake (VO2) and heart rate (HR) data. The rating of perceived exertion (RPE) was measurement before and immediately after the exercise tests.
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2

Comprehensive Participant Evaluation

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The experimental protocol involved two steps. The first consisted of an initial evaluation to collect participant’s identification data, perform anthropometric measurements, and assess pulmonary function. In the second step, conducted 24 h later, each participant’s heart rate was measured beat-by-beat during 30 min using a heart-rate meter (Polar S810i; Polar Electro, Kempele, Finland) for subsequent calculation of HRV indices.
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3

Incremental Cycling Exercise Assessment

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Anthropometric measurements and V˙O2peak were assessed during a preliminary session.
The V˙O2peak , defined as the highest 30-sec average, was
assessed by an incremental cycling exercise test (Velotron Racermate, Seattle,
WA, USA) starting at 70 W and increased by 35 W·min-1 until cadence
dropped below 60 rpm. Minute ventilation, carbon dioxide production and
V˙O2 was measured by a calibrated metabolic cart
(TrueOne 2400, ParvoMedics, Utah, USA) during the incremental exercise test.
Peak power output was prorated from the last completed stage plus the time in
the last uncompleted stage multiplied by 35 W [20 (link)]. Heart rate ([HR], Polar S810i, Polar
Electro Oy, Kempele, Finland) and RPE [21 (link)] were also assessed during the exercise.
In study 2, participants performed a standardised familiarisation trial adapted
from Lander et al. [22 (link)]
after the incremental exercise test. The familiarisation trial began at RPE 11
for 4 min and increased to RPE 13 (3 min), RPE 15 (2 min) and ended at RPE 19 (1
min).
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4

Cardiovascular Measurements in Children

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Blood pressure was measured indirectly using a stethoscope (Littman, Saint Paul, USA) and an aneroid sphygmomanometer (Welch Allyn, New York, USA) on the left arm of the children, following the criteria established by the VI Brazilian Guidelines on Arterial Hypertension [24 ]. HR was captured by means of a frequency meter, Polar S810i (Polar Electro, Kempele, Finland), previously validated for capture of RR intervals, as well as for HRV analysis using the interval series obtained [25 (link),26 (link)].
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5

Pediatric Autonomic Function Assessment

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The volunteers were evaluated in a room with a temperature between 21 and 23°C and humidity between 40 and 60%. All children were instructed not to drink ANS stimulants, such as coffee, tea and chocolate drinks, for a period of 12 hours prior to the evaluation, and not to perform intense physical activity on the day of the assessments. Before the autonomic assessment the children were instructed to remain silent and awake, spontaneously breathing at rest for 30 minutes in the supine position.
Before the start of the experimental procedure the children were identified by collecting the following information: age, sex, ethnicity, possible symptoms and associated pathologies.
After identification, weight, height, blood pressure, heart rate (HR), body fat percentage and casual blood glucose glycemia were measured. Next, a capture strap was placed at the distal third of the sternum and a heart rate receiver Polar S810i (Polar, Finland) on the wrist, to capture the heart rate beat-to-beat, with the child at rest, breathing spontaneously for 30 minutes in the supine position on a mattress. After the capture of HR at rest, the children performed the active orthostatic test and were then released.
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6

Autonomic Assessment in Children

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For autonomic assessment, a capture strap was positioned at the distal third of the sternum of the children and the heart rate receiver, Polar S810i (Polar®, Finland), on the wrist [25 (link),29 (link)] and HR beat-to-beat was recorded throughout the experimental protocol with a sampling rate of 1000 Hz.
The series of RR intervals was subjected to digital filtering complemented by manual to eliminate premature ectopic beats and RR artifacts and only series with more than 95% sinus beats were included in the study [29 (link),30 ]. HRV indices in the time and frequency domains were calculated using the software Kubios HRV (version 2.0) [31 (link)].
In the time domain, the SDNN and rMSSD indices were calculated. The SDNN index represents the standard deviation of all RR intervals [7 (link)] and the rMSSD the root mean square of the successive differences between adjacent normal RR intervals [7 (link)]. For the HRV analysis in the frequency domain the high frequency (HF, 0.15 to 0.4 Hz) and low frequency (LF, 0.04 to 0.15 Hz) spectral components were analyzed in ms2 and normalized units, and the ratio of these components (LF/HF ratio). Spectral analysis was calculated using the Fourier Transform algorithm [7 (link)].
For analysis of the HRV indices at rest and during the test, a five minute recorded interval was used and verified to contain a minimum of 256 beats.
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7

Cardiac Autonomic Regulation Assessment

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Before the assessment patients were maintained at rest for approximately 5 min to ensure stabilization of HR. HR and R-R intervals were recorded continuously during 10 min in supine position, using a Polar S810i system telemetry (Polar Electro, Kempele, OUL, Finland). Data were transferred to a computer through an interface (Polar Advantage, Kempele, OUL, Finland) for further analysis.
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8

Comparing Heart Rate Monitoring Devices

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During each trial participants wore a Polar HR monitor chest strap (T13, Polar Electro, OY, Finland) with the corresponding watch (Polar S810i, Polar Electro, OY, Finland), placed over the handrail of the treadmill and two Apple Watch Sport devices (Series 0, watchOS 2.0.1, Apple Inc., California, USA) – one on the left wrist and another on the right wrist. Both Apple Watches connected wirelessly via Bluetooth to two iPhone 5S smartphones (Apple Inc., California, USA). The sampling time for the Polar S810i HR monitor was set at 5 s intervals. Following exercise the HR data were transferred from the Polar S810i HR monitor to the Polar Pro Trainer 5 software. To measure HR on each Apple Watch, we used the ‘Workout’ app. The ‘Workout’ app nominally records HR at 5-s intervals. On cessation of each trial the HR data were synced automatically to the ‘Health’ database on its paired iPhone. To retrieve the raw HR and sampling time data from the ‘Health’ database, a bespoke iPhone app was written. The bespoke app was written in Xcode 7.2.1 using the language Swift 2.1 and using the methods provided by the HealthKit framework (Apple Inc., California, USA).
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9

Multimodal Recording of Brain and Physiological Activity

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The EEG was recorded by using the Micromed Brainquick amplifier (SD-LTM-32) and Micromed Brainspy software (Micromed, Venice, Italy). Recordings were made from Fp1, Fp2, F3, F7, Fz, F4, F8, C3, Cz, C4, T3, T4, P3, P7, Pz, P4, P8, O1, O2 placed according to the Int. 10–20 system with reference to the nose. All electrode impedances were kept at 5 kΩ or below. The EEG signals were continuously recorded and digitized at a sampling rate of 256 Hz. The EEG signal was amplified with a time constant of 0.3 s with a second order high-pass filter at 0.5 Hz and a low-pass filter at 120 Hz (frequency range: 0.5–120 Hz). Electrooculography (EOG) was monitored placed at the medial upper and lateral orbital rim of the right eye (time constant: 0.3 s; high pass filter: 0.1 Hz; low pass filter: 120 Hz; frequency range: 0.5–120 Hz). Two electrodes placed on the neck and on the shoulder recorded muscle activity. Heart rate (Polar S810i, Polar Electro, Buettelborn, Germany) was assessed continuously to control exercise intensity.
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10

Cardiopulmonary Exercise Testing Protocol

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The CPX was performed on a treadmill (Master ATL, Inbramed, Porto Alegre, Brazil) using a ramping protocol consisting of 5 min of incremental increase in speed from 0.8 km h−1 to 18 km h−1, followed by an incremental grade increase (0.5% each 30 s). This test was concluded when the athlete presented signs and/or symptoms of maximal exertion fatigue. The gas analyzer system was calibrated before the test following standard procedures (Balady et al, 2010 (link)). Ventilation and metabolic parameters were monitored and registered breath-by-breath (CPX-D/BreezeSuite 6.4.1, Medical Graphics, St Paul, MN). Electrocardiogram was continuously monitored (Active, Ecafix, Sao Paulo, Brazil) and heart rate (HR) was recorded by a digital telemetry system (Polar® S810i; Polar Electro Oy, Kempele, Finland). Blood pressure was assessed every 2 min. Using the ventilatory method, three independent evaluators determined the gas exchange threshold (GET) and the respiratory compensation point (RCP). The highest averaged VO2 value observed at the last 30 s of exercise was considered the VO2 peak. CPX was performed in a room with humidity between 35 and 40% and temperature between 24 and 25 °C (Table 1).
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