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NCT ID: NCT04297527 Recruiting - Chronic Pain Clinical Trials

Effect of Mulligan Mobilization in Chronic Non-Spesific Low Back Pain

Start date: June 14, 2017
Phase: N/A
Study type: Interventional

Fifty five participants diagnosed with CNSLBP, will randomized into three groups. Group I (18 subjects) will receive 15 sessions of Conventional Physiotherapy program (CPP) 5 times per week, Group II (19 subjects) will receive 9 sessions of SNAGs, and Group III will receive CPP plus SNAGs. Outcome measures are pain, ROM, spinal mobility, fear avoidance behaviour and function. Measurements will record before, after and 6 month after the end of the treatment.

NCT ID: NCT04297046 Completed - Ultrasonography Clinical Trials

Ultrasound-guided Two Different Type Blocks for Pain Relief in Totalabdominal Hysterectomy

Start date: April 1, 2017
Phase: N/A
Study type: Interventional

Effective analgesia after total abdominal hysterectomy is important for faster recovery and preventing complications which depend to pain. A multimodal and preventive approach is preferred to ensure adequate analgesia and to avoid side effects due to high doses of analgesics. The hypothesis was that the Quadratus Lumborum block (application of local anesthetics to the side of the abdomen) would be superior to Transversus Abdominis Plane block (application of local anesthetics in front of the abdomen) for analgesia before abdominal incision in total abdominal hysterectomy. The primary goal of the study was to evaluate the feasibility of ultrasound-guided Transversus Abdominis Plane block and Quadratus Lumborum block. The secondary goal was to evaluate postoperative adverse effects and patient satisfaction.

NCT ID: NCT04297007 Completed - Breast Cancer Clinical Trials

Pectoral Nerve Block Type-II and Rhomboid Intercostal Block for Pain Management Following Mastectomy Surgery

Start date: March 23, 2020
Phase: N/A
Study type: Interventional

Postoperative pain is an important issue in patients underwent mastectomy and axillary dissection surgery. Postoperative effective pain treatment provides early mobilization and shorter hospital stay. The US-guided pectoral nerve block (PECS) may be used for postoperative pain treatment following breast surgery. It is a novel interfascial block that was defined by Blanco. Rhomboid intercostal block (RIB) is a novel block and was first described by Elsharkawy et al. Local anesthetic solution is administrated between the rhomboid muscle and intercostal muscles over the T5-6 ribs. It has been reported that RIB may provide effective analgesia management for several breast surgeries. The primary aim of the study is to compare postoperative opioid consumption and the secondary aim is to evaluate postoperative pain scores (VAS), adverse effects related with opioids (allergic reaction, nausea, vomiting).

NCT ID: NCT04296929 Recruiting - Breast Cancer Clinical Trials

The Effect of Complex Decongestive Physiotherapy on Sensory Parameters in Breast Cancer Related Lymphedema.

Start date: November 28, 2019
Phase: N/A
Study type: Interventional

The aim of this study was to determine the effect of complex decongestive physiotherapy in women with unilateral breast cancer-related lymphedema on sensory parameters.

NCT ID: NCT04296539 Completed - Sedentary Behavior Clinical Trials

Compare the Scapular Muscular Endurance, Stabilization and Dyskinesis Parameters of Sedentary Individuals

Start date: March 20, 2019
Phase:
Study type: Observational

The aim of this study was to compare the parameters of scapular muscular endurance, scapular stabilization, scapular dyskinesia, upper extremity functional status and postural alignment of adult women aged between 40-65 years old who were performing clinical pilates exercises regularly compared with sedentary adult women in the same age group and to determine whether regular exercise had an effect on these parameters.

NCT ID: NCT04296526 Not yet recruiting - Sedentary Behavior Clinical Trials

Two-phase Transteoretic Model Research for Participation in Physical Activity

Start date: April 2021
Phase: N/A
Study type: Interventional

The purpose of the first phase of this study is to determine the physical activity (PA) barriers and motivational factors of university students and their body awareness using the transteoretic model (TTM). The aim of the second phase of the study is to evaluate the effectiveness of interventions aimed at eliminating barriers determined in students who are in the "precontemplation", "contemplation" and "preparation" stages according to TTM. Also it will be examined the effects of these interventions on PA level.

NCT ID: NCT04296409 Completed - Swallowing Disorder Clinical Trials

The Turkish Deglutition Handicap Index

Start date: June 22, 2022
Phase:
Study type: Observational

The purpose of this study is to test the reliability and validity of the The Turkish Deglutition Handicap Index among adult patients with swallowing disorders.

NCT ID: NCT04296084 Completed - Healthy Clinical Trials

Upper Extremity Kinematics During Walking

Start date: March 9, 2020
Phase:
Study type: Observational

Our aim is to investigate the upper extremity kinematics during walking in healthy individuals.

NCT ID: NCT04295629 Completed - Clinical trials for Ilioinguinal Nerve Block

The Effects of Ilioinguinal Nerve Block on Chronic Pain in Patients in Inguinal Hernia With Spinal Anesthesia

Start date: April 1, 2017
Phase: N/A
Study type: Interventional

Regional anesthesia is a popular anesthetic method in patients who will undergo an inguinal hernia operation. Researchers known that pain in the operating area is a complaint that impairs the quality of life for patients in the long term after the operation. In addition to regional anesthesia, has planned to investigate the effects of applying another drug near the surgery area on pain that may develop in the long term.

NCT ID: NCT04295083 Completed - ART Clinical Trials

Effect of Clay Based Group Study With Elderly Living Alone

Start date: December 27, 2017
Phase: N/A
Study type: Interventional

This study determines the effectiveness of clay-based group study on the loneliness and hopelessness levels in elderly living alone. For this, while the experimental group will six 1,5 h weekly of clay-based group study and interviewed face-to-face twice, the control group will interview face-to-face twice