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Heart Rate clinical trials

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NCT ID: NCT05641194 Recruiting - Sleep Clinical Trials

EaseAlert: Tactile Firefighter Alerting System

Start date: August 26, 2023
Phase: N/A
Study type: Interventional

The purpose of this research is to test a commercially viable Fire Fighter Altering System (FFAS) comprised of proprietary wearables and optional bed shakers called BunkAlerts; collectively "personal alerting devices" as an alternative approach to the traditional fire alarm system used in fire stations. Participants (fire fighters) will be asked to take part in the study to investigate the impact of the new FFAS on cardiovascular response and sleep. This study includes three phases: 1) baseline, 2) implementation of EaseAlert FFAS with traditional alarm, and 3) implementation of EaseAlert FFAS without traditional alarm. Participants will be asked to wear an Actigraph wGT3x-BT and Polar H10 device to record sleep and heart rate data for 12 days at work in addition to EaseAlert FFAS device for 8 out of the 12 days at work. They will also be asked to complete a questionnaire and complete daily journal entries.

NCT ID: NCT05600725 Completed - Cardiomyopathies Clinical Trials

Novel Cardiac Pacing to Initiate Cardiac Remodeling in Heart Failure

Start date: November 2, 2022
Phase: N/A
Study type: Interventional

This project utilizes a novel cardiac pacing approach hypothesized to initiate beneficial cardiac conditioning and remodeling over a period of time.

NCT ID: NCT05401435 Recruiting - Blood Pressure Clinical Trials

Reliability of Measuring Blood Pressure With a Smartwatch

Start date: May 4, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to verify the long-term accuracy of blood pressure and heart rate measurements by Samsung smartwatches between two consecutive calibrations compared to a standard digital tonometer used in clinical practice and for home measurement of these vital parameters.

NCT ID: NCT05401331 Completed - COVID-19 Clinical Trials

Effect of Mask Use on Hemodynamic Responses During Exertion

Start date: April 1, 2022
Phase: N/A
Study type: Interventional

The use of masks is a necessity due to the current pandemic conditions. The aim of the study is to examine the effects of the use of masks during effort on dyspnea and fatigue with hemodynamic parameters.

NCT ID: NCT05366049 Completed - Pain Clinical Trials

The Effect of Methods Used in Oral Antipyretic Administration on the Vital Findings of the Child With Fever

Start date: November 1, 2020
Phase: N/A
Study type: Interventional

Fever, one of the most common clinical journeys of childhood, makes up a fraction of emergency room admissions. About us-30. High fever, which is one of the first schools in infancy and childhood, can cause health problems such as not applying or starting the intervention. The most preferred method in the fire; antipyretic drug treatment in the hospital is routine . Antipyretics play a role in control plans and estimations of facts for cars of cars, the importance of word of mouth has some problems. In children, hospital, health care, injectors are grown from the breeder after completion, they can be created by red supplementation from the effects such as rearing without completion . resistance children; aspiration is risky, wrong dose is administered. It is stated in relation to teachers and verbal medicines for health. Hansen et al. Working with 61 babies aged 0-24 months, using a pacifier injector and a normal injector, children and temperature monitors. They are from the nipple injector used by mothers and women. There is a need for a new modification in the existing oral drug applications that will be able to support the adaptation and readiness of the child and to be able to effectively administer the drug. This work; Two different methods used to give antipyretic (medication pacifier and colored injector) were planned to be performed as pain, fever and purpose of life (respiratory rate, planning CTA) for the child.

NCT ID: NCT05358314 Completed - Clinical trials for Magnetic Resonance Imaging

Investigating Neuronal and Peripheral Markers of Brain Heart Interaction in Healthy Participants Under Stress

HRV_DB
Start date: February 1, 2022
Phase:
Study type: Observational

This study seeks to investigate which regions of the brain are relevant in the regulation of cardiac control and how the interplay between HRV and those regions change during different physiological states (stress versus relaxation). In order to achieve this, we will use functional magnetic resonance imaging (fMRI) during an experimental task consisting of deep breathing and a psychosocial stress task (Montreal Imaging Stress Task).

NCT ID: NCT05334628 Completed - Heart Rate Clinical Trials

The Effect of ESPB on Intraoperative Hemodynamics in VATS

Start date: April 11, 2022
Phase: N/A
Study type: Interventional

Video-assisted thoracic surgery (VATS) is frequently applied in thoracic surgery operations. VATS has become the standard procedure in minor and major lung surgeries. In recent years, regional anesthesia techniques have also been frequently applied to patients for pain relief. Thoracic paravertebral block (TPVB), erector spinae plane block (ESPB), and serratus anterior plane block (SAPB) are also among the regional anesthesia techniques frequently used in thoracic surgery. General anesthesia (GA) is the main method of anesthesia for thoracic surgery. However, GA can only inhibit the projection system of the cortical limbic system or hypothalamic cortex. GA cannot completely block the transmission of peripheral noxious stimulus to the central nervous system and cannot effectively inhibit the intraoperative stress response. With the addition of peripheral blocks such as TPVB, ESPB, and SAPB, more stable hemodynamics is expected by providing preemptive analgesia in patients. As a result of all these; In this study, we aimed to compare the intraoperative hemodynamic changes of patients who underwent preoperative ESPB in patients who will undergo VATS resection under GA with those who underwent postoperative ESPB.

NCT ID: NCT05302193 Recruiting - Blood Pressure Clinical Trials

Non-invasive Blood Pressure Measurement Using Samsung Smartwatch

Start date: February 15, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to verify the accuracy of blood pressure and heart rate measurement by Samsung smartwatches compared to a standard monitor of vital signs used in intensive care units.

NCT ID: NCT05261464 Recruiting - Heart Rate Clinical Trials

Heart Rate Controller in Computed Tomography Coronary Angiography

Start date: January 30, 2021
Phase: Phase 4
Study type: Interventional

Coronary computed tomography angiography (CCTA) is one of important non-invasive test for diagnosis of coronary artery disease. Cardiac motion artifact by heart rate (HR) has impact on CCTA interpretation. Current recommendation suggests HR reduction at less than 60 bpm with using of oral metoprolol. However, there are populations that are contraindicated for beta blockers. There were scantly data of calcium channel blocker and ivabradine. Moreover, there is no data comparing these 3 drug groups within single trial This double-blinded randomized controlled trial compares oral metoprolol immediate release, diltiazem immediate release and ivabradine with primary endpoint of patients' percentage to achieve target HR lower than 60 bpm prior to CCTA.

NCT ID: NCT05260489 Enrolling by invitation - Sleep Quality Clinical Trials

Apollo Remote Observational Sleep Study

Start date: January 18, 2022
Phase:
Study type: Observational

The purpose of this study is to examine how Transcutaneous Vibratory Stimulation (TVS) produced by the Apollo wearable affects sleep and cardiovascular function in a diverse real-world population of Apollo users.