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NCT ID: NCT05500638 Completed - Epilepsy Clinical Trials

Effect of VR-ESMEPP on Parents' Seizure Management

VR-ESMEPP
Start date: August 6, 2018
Phase: N/A
Study type: Interventional

Objective: This study aims to evaluate the knowledge, skills, and motivation of parents regarding management of epileptic seizures, by developing a "Virtual Reality Based Seizure Management Education Program for Parents (VR-ESMEPP). Method: This study is a double-blinded, pretest-posttest, observational randomized controlled study. The administration stage of the study was conducted between September 2018-February 2020 with parents of 91 children who were diagnosed with epilepsy and were being followed in the Pediatric Neurology Outpatient Department of Akdeniz University Hospital. The parents were distributed into groups with simple randomization (VR Group n=45-Control Group n=46). During the preparation stage of the study, data collection tools "Management-of-Epileptic Seizure-Training-Program-Prepared-with-Virtual-Reality-Technology" and "Patient Scenario Regarding Secondary Generalized Tonic-Clonic Epileptic Scenario with Aura" were prepared and integrated into the virtual reality glasses. In the administration stage, the intervention group was administered the pretest, then the training program, and a posttest immediately following the training. The participants were monitored on the 15th day. For the control group, a pretest, routine outpatient clinical practices, and a posttest were carried out; and the participants were monitored on day 15. In both groups, data were obtained with data collection tools that were integrated into the virtual reality glasses. An approval from the Ethics Committee of Akdeniz University, a written permission from the Akdeniz University Hospital, and informed consent from the parents were obtained to conduct the study.

NCT ID: NCT05500313 Completed - Clinical trials for Hypno-breastfeeding Education

The Effect of Education and Counseling Based on HypnoBreastfeeding

Start date: July 27, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to determine the effect of education and counseling based on the hypno-breastfeeding philosophy given in the antenatal period on only breastfeeding status, breastfeeding self-efficacy and breastfeeding motivation.

NCT ID: NCT05500287 Completed - Asthma in Children Clinical Trials

Virtual Care In Pediatric Asthma

Start date: March 14, 2021
Phase: N/A
Study type: Interventional

The purpose of this study was to determine the impact of virtual care for children with asthma on the disease management and quality of life of children with asthma.

NCT ID: NCT05500079 Active, not recruiting - Chronic Pain Clinical Trials

Transctunaous Pulsed Radiofrequency Therapy in Carpal Tunnel Syndrome

Start date: August 1, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to examine the effect of transcutaneous pulsed radiofrequency current in the treatment of carpal tunnel syndrome.

NCT ID: NCT05499897 Active, not recruiting - Clinical trials for Ultrasound giided Interscalene Block

The Effect of Interscalene Block on Wound Healing and Immunity in Open Shoulder Surgeries

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

In this study, investigators hypothesize the following: How will the amounts of these factors, which are involved in fibrin formation and wound healing, change after the block? If there is an increase, investigators can conclude that it has a positive effect on wound healing and immunity, if there is no change, it has no effect on wound healing and immunity.

NCT ID: NCT05499845 Completed - Smell Functions Clinical Trials

Effects of Different Anesthesia on Odor Memory

Start date: January 1, 2013
Phase:
Study type: Observational

This study aimed to research the effect of different general anesthesia administration on postoperative smell functions and memory.

NCT ID: NCT05499754 Completed - Clinical trials for Intracranial Pressure Increase

Effect of Different Supralottic Airway Devicess on Optic Nerve Sheath Diameter

Start date: July 1, 2019
Phase:
Study type: Observational

Direct laryngoscopy and tracheal intubation are associated with increases in intraocular pressure (IOP), intracranial pressure (ICP), heart rate (HR), and blood pressure. The use of supraglottic airway devices (SADs) are known to be beneficial in overcoming the disadvantages of laryngoscopy and tracheal intubation, especially ocular and pressure stress responses. In recent years, it has been reported that ultrasonographic measurement of optic nerve sheath diameter (ONSD) can be used in the diagnosis of increased ICP. The aim of our study is to compare the effects of Proseal laryngeal mask airway (pLMA), Suprem laryngeal mask airway (sLMA) and I-gel on hemodynamic response and ONSD during insertion in adult patients.

NCT ID: NCT05499689 Active, not recruiting - Migraine Disorders Clinical Trials

Transcutaneous Pulsed Radiofrequency in Migraine

Start date: June 22, 2021
Phase: N/A
Study type: Interventional

The aim of the investigator is to compare the efficacy of greater occipital nerve block and transcutaneous pulsed radiofrequency treatment in migraine.

NCT ID: NCT05499234 Completed - Labor Pain Clinical Trials

Epidural Tap in Labor Analgesia FOR LABOR ANALGESIA

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

The dural epidural tap method is performed by creating a dural perforation with a spinal needle placed through epidural needle, followed by placement of a catheter into the epidural space. No medications are administered through spinal needle. This prospective, randomized study includes 70 ASA II primigravid women with cervical dilatation between 4-6 cm and demanding epidural analgesia during spontaneous vaginal delivery.In the first group, 20 mL of 0.125% bupivacaine + 2 mcg/mL fentanyl solution and in the second group, 20 mL of 0.0625% bupivacaine + 2 mcg/mL fentanyl solution was administered as the first dose through the epidural catheter. Then, the visual analog scale (VAS) score was aimed to be below 4 in both groups.

NCT ID: NCT05499208 Completed - Clinical trials for Breast Feeding, Exclusive

Rotation and Movement System, Postpartum Cesarean Sections

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

In the first half hour of a cesarean advertisement, the service-oriented mother will not be mobile and will need support to get fit in bed and start getting started. The patient turning and movement system will provide a lot of convenience to the mother who does not have enough support. With the remote control system, the mother will be easily turned to the desired side in the bed and it will be ensured that she takes the desired position with less pain and more comfort.