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NCT ID: NCT05679505 Completed - Long COVID Clinical Trials

Vagus Nerve Stimulation for Post-COVID Syndrome

Start date: October 27, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to increase parasympathetic activity and decrease the severity of symptoms by providing vagal stimulation with the t-VNS method in order to suppress the increased sympathetic activity in patients with prolonged Covid symptoms.The main question[s] it aims to answer are: Question 1:Is left ear transcutaneous vagus nerve stimulation effective in suppressing the symptoms of patients in Post Covid syndrome? Question 2:Is bilateral auricular transcutaneous vagus nerve stimulation effective in suppressing the symptoms of patients in Post Covid syndrome? A 5-minute heart rate variability measurement will be performed to measure the effectiveness of vagus nerve stimulation in participants.HRV is a non-invasive method used to evaluate ANS activity and is a measure of heart rate change over a period of time

NCT ID: NCT05679453 Completed - Pain, Acute Clinical Trials

Lornoxicam Versus Etodolac After Third Molar Surgery

Start date: July 20, 2022
Phase: Phase 4
Study type: Interventional

Our study aimed to compare the effect of lornoxicam and etodolac on postoperative pain, edema and trismus following lower third molar extraction

NCT ID: NCT05679219 Recruiting - Virtual Reality Clinical Trials

Video-Based Gaming Therapy in Pes Planus Rehabilitation

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

Purpose: It is aimed to evaluate the effect of structured exercise, wii-based exergame and wii-based serious game exercise protocols on functional parameters in individuals with pes planus. Method: 69 individuals with Pes Planus between the ages of 18-25 who met the inclusion criteria will be included in the study. Pedobarographic analysis, navicular drop test, flexibility, balance, femoral anteversion and lower extremity muscle strength measurements will be performed on the participants before and after the treatment. In addition, demographic information of individuals will be recorded through a survey. After the initial evaluation, participants will be randomly assigned to one of three groups. All subjects participating in the study will be treated under the supervision of a specialist physiotherapist for a total of 18 sessions, 3 days a week for 6 weeks, 40 minutes each session. Structured exercise group; short foot exercise, towel curl exercise, toe walking, heel walking, tandem walking, eccentric gastrosoleus stretching at the edge of the stairs, collecting objects from the ground with the toes, balance exercises on one foot will be performed. Penguin Slide, Tightrople Tension, Tilt Table, Soccer Heading and Balance Bubble games, which are balance games of the Nintendo wii game console, will be played for the Wii-based exergame group for 8 minutes each and a total of 40 minutes per session. For Wii-based serious game group, 3 games, Balance Surf, Balance Adventure and Balance Maze, which are among the balance games included in the Becure Balance System that works integrated with the Wii Balance Board, will be played for 40 minutes each session under the supervision of an expert physiotherapist. After the treatment, all measurements will be repeated, the difference between before and after treatment and the superiority of different treatment protocols will be tried to be determined.

NCT ID: NCT05678920 Completed - Validation Clinical Trials

Validation of the Turkish Version of the Modified Early Obstetric Warning Systems (MEOWS) Charts

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

It was aimed to study MEOWS on patients in the obstetrics clinic and to evaluate the performance of this scale as a screening tool and to contribute to its usability in Turkey by translating MEOWS into Turkish.

NCT ID: NCT05678855 Completed - Nursing Students Clinical Trials

The Effect of multımedıa-based educatıon ın dıstance learnıng on nursıng Students'

Start date: February 10, 2021
Phase: N/A
Study type: Interventional

Abstract Objective: In this study, it is aimed to evaluate the effect of multimedia teaching materials on students' academic achievement and motivation in teaching nursing process course. Design: Randomized controlled trial. Settings: Public university. Participants: The research was carried out on first year nursing students (N=70). Methods: Data; were collected using the introductory features form, academic achievement evaluation (quiz) and Instructional Materials Motivation Questionnaire. Research data were collected using online questionnaires. The experimental group students were presented with the contents of the nursing process course, which was prepared with multimedia materials for two hours in seven weeks with distance education. The control group students were taught by distance education and traditional lectures for two hours in seven weeks.

NCT ID: NCT05678842 Completed - Weight, Body Clinical Trials

Balance and Weight Distributions at Kneeling

Start date: February 16, 2022
Phase:
Study type: Observational

This study aims to examine balance parameters and weight distributions at different kneeling positions.

NCT ID: NCT05678829 Recruiting - Virtual Reality Clinical Trials

Reproductive Health and Family Planning

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

The aim of this study is to measure the knowledge and attitude levels of women who play a key role in society on reproductive health and family planning, and to determine the changes in their attitudes and behaviors after face-to-face training with virtual reality application.

NCT ID: NCT05678790 Completed - MPAN Clinical Trials

Mitochondrial Membrane Protein Neurodegeneration (MPAN)

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

The purpose of this case study was to investigate the effects of therapeutic intervention in 9- and 12-year-old brothers with MPAN. The main hypothesis it aims to answer is: -A 6-week balance and coordination focused rehabilitation program improves independence and gait parameters in patients with MPAN.

NCT ID: NCT05678777 Recruiting - Regional Anesthesia Clinical Trials

Use of Galvanic Skin Response to Measure Peripheral Block Activity

Start date: January 30, 2022
Phase:
Study type: Observational

the investigators aim in this study is to determine whether the block is successful in successful infraclavicular brachial plexus blocks performed with USG, according to the change in GSR value in the upper extremity blocked due to sympathetic nerve blockade. Block success will be evaluated by sensory and motor examination of the blocked arm.

NCT ID: NCT05678686 Completed - Stroke Clinical Trials

Investigation of The Effects of Different Exercise Methods on Swallowing Function in Stroke Patients

Start date: October 3, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to examine the effects of PNF (proprioceptive neuromuscular facilitation) and CTAR (Chin Tuck Against Resistance) exercises on swallowing rehabilitation in stroke patients. In addition another aim is to examine the effects of these exercises on the swallowing function, quality of life, functional independence and functional oral intake of individuals, and to investigate the superiority of the exercises to each other in line with these features.