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Somatoform Disorders clinical trials

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NCT ID: NCT05995639 Not yet recruiting - Clinical trials for Myofascial Pain Syndrome

Dry Needling Versus Ozone in Myofascial Pain Syndrome

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

The aim of this study is to compare the effects of dry needling treatment (DN) and ozone treatment on pain and functionality in individuals with myofascial pain syndrome affecting the upper trapezius (UT) region.

NCT ID: NCT05882838 Not yet recruiting - Clinical trials for Myofascial Pain Syndrome

The Level of Knowledge and Awareness of Myofascial Pain Syndrome in the Turkish Population

Start date: November 1, 2023
Phase:
Study type: Observational [Patient Registry]

This study aimed to assess the level of knowledge and awareness of myofascial pain syndrome (MPS) among the Turkish population.

NCT ID: NCT05854446 Not yet recruiting - Clinical trials for Myofascial Pain Syndrome

Delphi Study on Myofascial Pain Syndrome Challenges in Turkey: Patient Journey, Burden, Diagnosis & Treatment Needs.

Start date: June 1, 2023
Phase:
Study type: Observational

Myofascial pain syndrome is a chronic pain disorder that affects many people in Turkey. This research study aims to explore the challenges faced by patients with myofascial pain syndrome in Turkey, including the disease burden, patient journey, and unmet diagnosis and treatment needs. The study will utilize the Delphi methodology, which involves gathering input from a panel of experts over multiple rounds to achieve consensus on the topic. The results of this study will shed light on the current state of myofascial pain syndrome management in Turkey and provide insights into the areas where improvements can be made.

NCT ID: NCT05710627 Not yet recruiting - Clinical trials for Greater Trochanteric Pain Syndrome

Evaluation of TENEX for Greater Trochanteric Pain Syndrome (GTPS)

RCT GTPS
Start date: February 2025
Phase: N/A
Study type: Interventional

The aim of this study is to characterize the efficacy of percutaneous tenotomy (PUT) using TENEX®, a device used for the treatment of various tendinopathies. In this study an ultrasound (US) is performed to guide the partial release of gluteus medius and minimus and Iliotibial band tendons in patients diagnosed with refractory Greater Trochanteric Pain Syndrome (GTPS) vs control. The study team hypothesizes that PUT can improve the pain level and function for individuals suffering with GTPS. The study will assess walking, standing, and side-lying tolerance, as well as medication utilization. The investigator team predicts that this percutaneous outpatient procedure can decrease pain and medication utilization while increasing mobility.

NCT ID: NCT05659199 Not yet recruiting - Clinical trials for Chronic Pelvic Pain Syndrome

Extracorporeal Shockwave and Myofascial Release Therapy in Chronic Pelvic Pain Syndrome

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

The primary aims of this research are three folds: (1) To identify more relatively effective interventions for improving pain symptoms in CP/CPPS patients. (2) To ascertain the correlation between PFM elastic modulus and tenderness symptoms. This may find a more objective method of assessing efficacy. (3) To determine the correlation between the intensity of the sympathetic response and the patient's symptoms and to explore other possible pathogenetic mechanisms.

NCT ID: NCT05469672 Not yet recruiting - Clinical trials for Low Level Laser Therapy

The Effect of Laser Therapy in the Management of Adhesive Capsulitis: a Randomized Clinical Trial

Start date: September 25, 2022
Phase: N/A
Study type: Interventional

In this study, it was aimed to compare the effects of low-level laser therapy (LLLT) and high-intensity laser therapy (HILT) on shoulder joint range of motion, level of pain and functional status in patients with adhesive capsulitis

NCT ID: NCT05383781 Not yet recruiting - Clinical trials for Patellofemoral Pain Syndrome

Effect of Short Foot Exercise in Treatment of Patients With Patellofemoral Pain Syndrome

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

Purposes of the study To investigate the effect of adding Short foot exercise on patellofemoral pain syndrome on knee Pain, Function, Balance and abductors, quadriceps Muscle strength.

NCT ID: NCT05366517 Not yet recruiting - Clinical trials for Chronic Prostatitis With Chronic Pelvic Pain Syndrome

Repeating LiST for Refractory Non-bacterial Prostatitis/Pelvic Pain Syndrome

Start date: September 2022
Phase: N/A
Study type: Interventional

The aim of the study is to investigate the efficacy and safety of LiST retreatment for CP/CPPS patients.A total of 50 patients with CP/CPPS diagnosis who were previously treated with 6 sessions of LiST will participate in this study.The primary study parameter is the CP/CPPS-related pain complaints and it will be assessed by the NIH-CPSI

NCT ID: NCT05359523 Not yet recruiting - Clinical trials for Myofascial Pain Syndrome

Ultrasonographic Muscles and Fascia Measurement With Myofascial Pain Syndrome

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

Pathologies in the trapezius muscle and rhomboid muscle are important in the course and treatment of the disease in patients with myofascial pain syndrome.

NCT ID: NCT05327569 Not yet recruiting - Clinical trials for Patellofemoral Pain Syndrome

The Efficacy of Myofascial Chain Release Techniques in Patients With Patellofemoral Pain Syndrome.

Start date: September 20, 2022
Phase: N/A
Study type: Interventional

The aim of this study was to evaluate the effects of myofascial release techniques applied on the superficial anterior myofascial chain of the body on pain, functional status, posture, biomechanical and viscoelastic properties of myofascial tissues in patients with patellofemoral pain syndrome. There will be two groups in this study. Each group will consist of 30 patients aged 25-50 years with patellofemoral pain syndrome. A total of 60 participants will take part in the study. Conventional physiotherapy will be applied to the control group, while myofascial release techniques will be applied to the experimental group in addition to conventional physiotherapy. Treatment programs will be applied to both groups 2 days a week for 6 weeks. Postural problems that can be seen in the superficial anterior myofascial chain line will be evaluated. These problems: forward head, q-angle, genu varum, genu valgum, foot postural problems and pelvic tilt. In addition to all these assessments, knee pain, lower extremity functionality and biomechanical properties of the anterior myofascial tissue will be evaluated.