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NCT ID: NCT06407596 Completed - Hemiplegia Clinical Trials

HILT or Conventional Combined Physical Therapy, in the Management of Hemiplegic Shoulder Pain

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

Background: Hemiplegic shoulder pain is one of the most common complications after a stroke. There are many treatment strategies for this complication. High-intensity laser therapy (HILT) is a new treatment option, and we aimed to compare the effectiveness of conventional electrotherapy agents and HILT in this study. Patients and methods: Participants (N = 42) were randomized into the HILT (n = 21) and TENS+US (n = 21) groups. Group 1 received 3 sessions of HILT per week for 3 weeks in addition to a therapeutic exercise program that performed 5 sessions per week for 3 weeks. Group 2 received conventional physical therapy and a therapeutic exercise program for HSP of 5 sessions per week for 3 weeks. Patients were assessed before and after treatment on the on the 6th week for radiological evaluation with ultrasonography and for clinical parameters with VAS, AMAT, MRS, and FIQ scores.

NCT ID: NCT06407531 Recruiting - Colonoscopy Clinical Trials

Before Colonoscopy Effect of Virtual Reality Application on Anxiety and Vital Signs

Start date: November 21, 2023
Phase: N/A
Study type: Interventional

This study was planned to examine the effect of virtual reality application on the patient's anxiety and vital signs before colonoscopy. The hypotheses of the research are as follows: H1: Virtual reality application before colonoscopy has an effect on patients' anxiety and vital signs. H0: Virtual reality application before colonoscopy has no effect on patients' anxiety and vital signs. Before colonoscopy, patients in the study group will be asked to watch videos using virtual reality glasses.

NCT ID: NCT06407492 Recruiting - Chronic Pain Clinical Trials

Complementary Medicine Practices in Chronic Low Back Pain: Randomized Controlled Trial

Start date: May 9, 2024
Phase: N/A
Study type: Interventional

To compare the effectiveness of classical physiotherapy and leech therapy in patients with chronic low back pain.

NCT ID: NCT06407479 Recruiting - Chronic Pain Clinical Trials

Comparison of Eccentric Muscle Training and Proprioceptive Neuromuscular Facilitation Techniques in Neck Pain

Start date: May 9, 2024
Phase: N/A
Study type: Interventional

It was aimed to compare the eccentric exercise training given to the neck muscles of people with non-specific neck pain and the proprioceptive neuromuscular facilitation (PNF) technique on pain, endurance and functionality.

NCT ID: NCT06407466 Recruiting - Clinical trials for Sports Physical Therapy

The Effect of Soft Tissue Mobilization and Kinesio Taping Applied to Athletics Athletes on Sports Performance

Start date: May 9, 2024
Phase: N/A
Study type: Interventional

The aim of the research is to evaluate the effects of tool-assisted soft tissue mobilization and kinesiology tape applications applied to the Hamstring muscle on balance, agility and jumping in athletics athletes.

NCT ID: NCT06407453 Recruiting - Neck Pain Clinical Trials

Effectiveness of Exercise Given With Ergonomics Training in Tea Workers

Start date: May 9, 2024
Phase: N/A
Study type: Interventional

The aim of our study is to investigate the effectiveness of exercise against work-related musculoskeletal disorders in tea workers.

NCT ID: NCT06407440 Recruiting - Clinical trials for Work-related Illness

The Effect of Exercise Given to Cashiers Along With Ergonomics Training on Pain and Work Performance

Start date: May 9, 2024
Phase: N/A
Study type: Interventional

The aim of the study is to examine the effectiveness of the exercises given to cashiers through ergonomics training.

NCT ID: NCT06407414 Recruiting - Clinical trials for Patellofemoral Pain Syndrome

Effectiveness of Neuromuscular Exercise in Patellofemoral Pain Syndrome

Start date: May 14, 2024
Phase: N/A
Study type: Interventional

The aim of the study is to investigate the effects of a neuromuscular exercise program on strength, balance, sleep quality and functionality in individuals with Patellofemoral pain syndrome.

NCT ID: NCT06407362 Completed - Perfusion Index Clinical Trials

Effects of Volume and Pressure-Controlled Ventilation on Cerebral SpO2, PI, and PVI Index in Septoplasty

Start date: May 15, 2021
Phase:
Study type: Observational

Objective: This study was designed to evaluate the accuracy of Pleth Variability Index (PVI), Perfusion Index (PI) and Regional Oxygen Saturation (rSO2) in both ventilation modes in patients undergoing septorhinoplasty operation under general anaesthesia. Materials and Methods: After anaesthesia induction, ventilation was provided with volume control for 20 minutes. Heart Rate (HR), PI, PVI, Oxygen Saturation (SpO2), Non-Invasive Blood Pressure (NIBP) and rSO2 values were recorded every 5 minutes. At the 20th minute of the surgical procedure, the ventilation mode was set as the pressure-controlled mode. After switching to pressure-controlled mode, HR, PI, PVI, SpO2, NIBP and rSO2 values were recorded every 5 minutes for 20 minutes.

NCT ID: NCT06407037 Recruiting - Postoperative Pain Clinical Trials

Comparison of Erector Spinae Plane Block and Serratus Posterior Superior Intercostal Plane Block

Start date: December 27, 2023
Phase: N/A
Study type: Interventional

Breast cancer is the most common malignancy in women. Modified radical mastectomy, a surgical procedure in the treatment of breast cancer, is one of the standard treatments. Postoperative pain can seriously reduce the quality of life in patients, and inadequately treated acute pain can trigger chronic pain syndrome. Therefore, thoracic paravertebral block and thoracic epidural block are effective in postoperative analgesia. However, the use of these blocks is limited due to complications. In recent years, less invasive blocks, such as pectoral nerve block (PECS I-II), Serratus anterior plane block (SAPB), Erector spinae plane block (ESPB), and Serratus Posterior Superior intercostal Plane Block (SPSİPB) have been applied. In this study, it was aimed to compare the analgesic effectiveness of ESPB and SPSİPB applications in patients undergoing breast surgery.