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NCT ID: NCT05675514 Completed - Clinical trials for Sports Physical Therapy

Investigation of the Effectiveness of Myofascial Release Technique in Young Basketball Players

Start date: January 10, 2023
Phase: N/A
Study type: Interventional

In this study, it is aimed to remove the limitations that cause asymmetry and weak connections in functional movement patterns with myofascial relaxation method to be applied to certain muscles and to remove the obstacles in front of the power factor as a result of its application, to reach the highest efficiency of the athlete's performance and to reduce the risk of injury in the musculoskeletal system.Study; It was planned as a control group (n:30) and an intervention group (n:30). Apart from routine training, the intervention group will be treated twice a week for 6 weeks before the training. On the other hand, no application will be made to the control group other than routine training. The evaluations are; It will be done at the beginning of the study and after the 6-week period.

NCT ID: NCT05675488 Completed - Trigger Finger Clinical Trials

Ultrasound Features of Trigger Finger

Start date: January 14, 2023
Phase:
Study type: Observational

Our aim in this study; to compare the ultrasound findings seen in trigger finger patients with healthy volunteers. Thus, ultrasound findings associated with trigger finger development will be documented

NCT ID: NCT05675358 Completed - Pain, Acute Clinical Trials

Virtual Reality on Pain, Fear, and Emotional Appearance During Phlebotomy in Pediatric Hematology and Oncology Patients

VR-PHO
Start date: March 3, 2022
Phase: N/A
Study type: Interventional

In this study, the effect of virtual reality, which is one of the pain relief methods, on the pain, fear and emotional appearance associated with the procedure, was evaluated in children aged 4-12 years who will undergo phelobotomy in a Pediatric Hematology and Oncology outpatient clinic.

NCT ID: NCT05674461 Active, not recruiting - Postpartum Period Clinical Trials

The Effect of WhatsApp-Based and Face-to-face Nursing Education on Mothers' Quality of Life and Traditional Practices

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

Introduction: The postpartum period is very important and is a suitable period for women to gain healthy lifestyle behaviors. Studies in the literature show that women with high quality of life have a more comfortable postpartum period. If the needs of women are not met in the postpartum period, there may be an increase in traditional practices for mothers. For this reason, postpartum education is very important for maternal health. Various ways can be used to provide education to mothers. With the development of technology, education given over mobile applications has often found a place in studies. The face-to-face education format, on the other hand, remains up-to-date. It is not known for certain which form of education is superior to the other. Testing the superiority of these two training methods to each other will eliminate the question marks in this area. Purpose: To determine the effectiveness of WhatsApp-based and face-to-face nursing education and counseling given in the postpartum period on mothers' quality of life and traditional practices. Method: The experimentally planned study will consist of three groups including WhatsApp, face-to-face and control group. The universe of the research will be composed of women hospitalized in Sivas Numune Hospital Aseptic Service. A total of 180 people will be taken into the sample of the research, 60 of which are in the WhatsApp experimental group, 60 in the face-to-face experimental group and 60 in the control group. Training videos for the postpartum period will be sent to the WhatsApp experimental group via WhatsApp. Face-to-face training will be given to the women in the face-to-face experimental group by the researcher, and the handbook containing the training content will be distributed to the women. Women in both experimental groups will be supported by providing counseling over the phone (message, meeting if needed). No attempt will be made to the control group. The participant introduction form and the Turkish version of the world health organization quality of life scale (WHOQOL-BREF-TR) will be used to evaluate the data of the study. The data will be evaluated with the SPSS 28 program.

NCT ID: NCT05674201 Completed - Deep Sedation Clinical Trials

Effects Of Propofol-Dexmedetomıdıne And Propofol- Remıfentanıl In Hysteroscopıc Operations.

Start date: June 17, 2021
Phase:
Study type: Observational [Patient Registry]

In our study, the investigators aimed to compare the effects of dexmedetomidine-propofol and remifentanil-propofol combinations on perioperative spontaneous respiration, hemodynamics, recovery, participants, surgeon and anesthetist satisfaction in hysteroscopy, which is one of the ambulatory surgery.

NCT ID: NCT05674006 Completed - Anesthesia, Local Clinical Trials

Ultrasound Guided Sacral Erector Spina Plane Block as a Main Anesthetic Method

ESP
Start date: January 25, 2023
Phase:
Study type: Observational

The goal of this retrospective observational study is to demonstrate investigators' experience of Ultrasound guided Sacral Erector Spina Plane Block as an anesthetic technique in patients underwent sacral plastic and reconstructive surgeries. The main question[s] it aims to answer are: - block indication, level - results, side effects and complications

NCT ID: NCT05673863 Completed - Child Sexual Abuse Clinical Trials

Resilience in Girls Victims of Sexual Abuse

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

İn this study, it was aimed to examine the effectiveness of the psychological resilience program for adolescent girls after sexual abuse.This study is a randomized controlled trial.

NCT ID: NCT05673707 Recruiting - Clinical trials for Airway Complication of Anesthesia

The Effect of Thyromental Height and Other Difficult Airway Evaluation Parameters

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

Many changes occur in the body with age. There are difficulties in endotracheal intubation and the placement of supraglottic airway devices (LMA) in elderly patients due to changes in the tooth and facial structure, and a decrease in temporomandibular joint and neck movements. In the literature, there are studies on the relationship between thyromental height measurement and endotracheal intubation difficulty, but there is no study on the relationship between thyromental height measurement and laryngeal mask placement difficulty.

NCT ID: NCT05673642 Recruiting - Low Back Pain Clinical Trials

Effect of Myofascial Release Technique Applied to in Patients With Temporomandibular Dysfunction

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

We aim to compare the effectiveness of MFR and exercise therapy on mobility and function by investigating the effectiveness of the Myofascial Release Technique (MFR), which we will apply to the muscles we choose related to the facial system connection in participants with temporomandibular dysfunction (TMD) and low back pain.

NCT ID: NCT05673291 Not yet recruiting - Clinical trials for Musculoskeletal Pain

Posture and Musculoskeletal Pain in Dentists

Pain
Start date: February 10, 2023
Phase:
Study type: Observational [Patient Registry]

Objectives: Musculoskeletal problems have been a concern in dentists for years. The aim of this study is to evaluate the relationship between posture and musculoskeletal pain in dentists.