Clinical Trials Logo

Filter by:
NCT ID: NCT06376825 Recruiting - Clinical trials for Burnout, Professional

The Efficacy and Acceptability of an Internet-Based Self-Help Program to Reduce Burnout

Start date: April 15, 2024
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to determine whether an internet-based self-help program reduces burnout in teachers. The study will also evaluate the program's acceptability which means assessing the extent to which users complete the program and find it useful. The main questions it aims to answer are: - Does the program reduce the level of burnout in teachers? - Does the program contribute to an increased sense of meaning for teachers? - How much of the program do teachers finish?

NCT ID: NCT06376370 Enrolling by invitation - Quality of Life Clinical Trials

The Effect of a Computer-Assisted Rehabilitation Program on Epilepsy Patient

Start date: April 26, 2024
Phase: N/A
Study type: Interventional

The aim of this study is to examine the effects of the RehaCom Computer-Assisted Rehabilitation Program Applied to Epilepsy Patients on Self-Management, Cognitive Function and Quality of Life.

NCT ID: NCT06376357 Enrolling by invitation - Breast Neoplasms Clinical Trials

The Effect of Foot Massage With Roles on Cancer Patients

Start date: April 27, 2024
Phase: N/A
Study type: Interventional

It was aimed to examine the roles in the management of treatment-related peripheral neuropathy in cancer patients receiving taxane-based chemotherapy and the effect of foot massage on neuropathy and quality of life.

NCT ID: NCT06376344 Enrolling by invitation - Cancer Clinical Trials

The Effect of Tennis Ball on Balance and Quality of Life in Cancer Patients With Neuropathy.

Start date: April 28, 2024
Phase: N/A
Study type: Interventional

This research; It was aimed to evaluate the effect of myofascial release using a tennis ball on balance and quality of life in cancer patients who developed peripheral neuropathy.

NCT ID: NCT06376123 Not yet recruiting - Clinical trials for One-lung Ventilation

Nomogram for Prediction of Alveolo-arterial Gradient During One-lung Ventilation

Start date: May 1, 2024
Phase:
Study type: Observational [Patient Registry]

The cause of hypoxia during one-lung ventilation is a common anaesthetic problem seen during thoracic surgery and is associated with increased fraction of shunted blood. This shunt occurs because the lung not participating in respiration stops saturating the blood with oxygen. The importance of our study is to collect some of the patient's parameters on a nomogram in the preoperative period, to predict the shunt fraction that will occur during one-lung ventilation and to make preparations and interventions accordingly.

NCT ID: NCT06375980 Completed - Lung Injury Clinical Trials

Intraoperative Mechanical Power and Ventilation-Associated Lung Injury: Assessing Complications

Start date: April 1, 2022
Phase:
Study type: Observational [Patient Registry]

This study investigates the relationship between intraoperative mechanical power and postoperative pulmonary complications in patients undergoing major abdominal surgery. We record mechanical ventilation parameters and surgical characteristics, assessing the incidence of pulmonary complications within 24 hours postoperatively

NCT ID: NCT06375863 Completed - Long QT Syndrome Clinical Trials

QT Changes in Geriatric Patients: a Comparison of Spinal and General Anesthesia

Start date: March 29, 2023
Phase: N/A
Study type: Interventional

QT interval, defined as the time between the beginning of the QRS complex and the end of the T wave in electrocardiography (ECG), is an indicator of depolarization and repolarization of the myocardium.11 Prolongation of the heart rate corrected QT (QTc) interval reflects electrical instability of ventricles and is associated with life-threatening ventricular arrhythmias, including torsade de pointes, ventricular fibrillation and sudden cardiac death. Spinal anesthesia can cause profound prolongation of the QTc interval due to disparity between lumbar and thoracic sympathetic activity following subarachnoid block. Meanwhile inhalational anesthetics, sevoflurane, isoflurane, and desflurane are known to prolong QTc interval and intravenous anesthetics such as propofol, thiopental, etomidate and ketamin can also cause remarkable prolongation of the QTc interval. Moreover laryngoscopy and intubation may contribute to prolongation of the QTc interval because of the sympathetic stimulation. Over the years it has been occurred an increase in the proportion of elderly population requiring surgical anesthesia. The incidence of ventricular arrhythmias increases in advancing age even in the absence of underlying heart disease and elderly patients have reduced physiological functions and poor tolerance to anesthesia. However the choice of anesthesia type is critical in this population. To the best of knowledge, there was no published study to compare spinal anesthesia and inhalational anesthesia in elderly patients with regard to the QT interval changes. Investigators aimed to investigate the effects of spinal anesthesia on QT, QTc intervals and to compare general anesthesia with sevofluran in elderly patients.

NCT ID: NCT06375837 Recruiting - Tooth Diseases Clinical Trials

Comparative Evaluation of an Alkasite-based Restorative Material and Two Different Resin Composites

Start date: April 15, 2024
Phase: N/A
Study type: Interventional

The clinical performance of an an alkasite-based restorative material and two different resin composites will be evaluated and compared in non-carious cervical lesions. After recruiting participants with at least three non-carious cervical lesions, all restorations will be placed by a single clinician. Lesions will be divided in three groups: an alkasite-based restorative material (Cention N, Ivoclar Vivadent, Schaan, Liechtenstein (CN)), hybrid resin composite (Gradia Direct Anterior, GC, Tokyo, Japan (GD)) and a highly filled flowable resin composite ((G-aenial Universal Flo, GC, Tokyo, Japan (GF)). All restorative procedures will be conducted according to manufacturers' instructions. Restorations will be scored using FDI criteria. Descriptive statistics will be performed using chi-square tests.

NCT ID: NCT06375785 Completed - Elderly People Clinical Trials

Two Different Exercise Methods in Geriatrics

Start date: March 1, 2023
Phase: N/A
Study type: Interventional

The aim of the study is to compare slow rhythmic exercises with large amplitude exercises in elderly people

NCT ID: NCT06375603 Completed - Nerve Block Clinical Trials

Nerve and Plane Block Data Collection Study for the Development of Artificial Intelligence-assisted Software

Start date: December 1, 2022
Phase:
Study type: Observational

The primary objective of this observational study is to acquire ultrasound images (raw data) from nerve and plane block regions to develop artificial intelligence-guided nerve block software (Nerveblox). The study aims to acquire raw ultrasound video from 200 volunteers' planned nerve and plane block regions. These participants will undergo ultrasound scans administered by expert clinicians proficient in these techniques in their clinical practice. The data collection devices utilized in this study are FDA-cleared general-purpose ultrasound devices.