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Myofascial Pain Syndromes clinical trials

View clinical trials related to Myofascial Pain Syndromes.

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NCT ID: NCT03008837 Completed - Fibromyalgia Clinical Trials

Feasibility Study: fMRI Evaluation of Auricular PENFS for Fibromyalgia

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

Given recent increasing opioid-related deaths and evidence showing against the use of opioids for non-malignant chronic pain, there is growing need for non-narcotic pain management. Fibromyalgia is a difficult to treat chronic pain condition that is often treated with opioids despite existing evidence. The prevalence of fibromyalgia is increased among Veterans returning from the gulf war and is already a significant burden in senior Veterans who may have suffered with chronic pain for decades already. Many treatment options for fibromyalgia carry intolerable side effects. PENFS (percutaneous electrical neural field stimulation) is a FDA-approved, non-pharmacologic therapy that is currently utilized within the military and VA system, but sufficient evidence regarding its outcomes and neural mechanisms have not been adequately investigated. An understanding of its neural underpinnings and analgesic effects could lead to 1) improvements in pain management and quality of life, 2) cost-savings and 3) development of new techniques to address pain.

NCT ID: NCT03006822 Completed - Clinical trials for Myofascial Pain Syndrome

Time Effect of the Pressure Release Technique Application in the Latent Myofascial Trigger Points

Start date: March 15, 2017
Phase: N/A
Study type: Interventional

Background: Latent myofascial trigger points (MTrPs) of the levator scapulae are high prevalent and may influence the neck and shoulder conditions. The pressure release is one of the most recommended manual therapy techniques. Objective: To determine the time effect of the pressure release technique application in the latent MTrPs of the levator scapulae muscle. Design: A three-arm (1:1:1 ratio), double-blinded, parallel, randomized clinical trial. The manual technique than us apply, be sustained digital pressure with thumbs or with the 2nd-3rd fingers on the PGM below the pain threshold and gradually increases up to a ceiling of tissue resistance (barrier), as decreases, adds more pressure. different times of sustained pressure and the number of repetitions depending on time 30 (group 1, acts as a control), 60 (group 2) and 90 seconds (group 3) shall apply.

NCT ID: NCT03004911 Completed - Fibromyalgia Clinical Trials

Development of a Mobile Application to Promote Self-care in Patients With Fibromyalgia

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

The purpose of this study is to test the efficacy of a mobile application named ProFibro to promote self-care, and improve symptoms and health-related quality of life in Brazilian patients with fibromyalgia.

NCT ID: NCT02969707 Completed - Fibromyalgia Clinical Trials

Use of Repetitive Transcranial Magnetic Stimulation to Augment Hypnotic Analgesia

Start date: April 24, 2017
Phase: N/A
Study type: Interventional

The investigators plan to use functional neuroimaging (fMRI) to understand the brain systems affected when hypnosis and hypnotic analgesia are augmented with repetitive transcranial magnetic stimulation (rTMS), a form of non-invasive brain stimulation to 100 people with fibromyalgia, a chronic pain condition. The investigators will measure the effect of rTMS-augmentation on the brain networks underlying hypnotizability, as well as the effect of rTMS-augmentation on hypnotic analgesia networks. The investigators hope to demonstrate that a combination of these psychological and neuromodulatory treatments will be more effective than hypnosis alone, thereby enhancing the depth of hypnosis, range of hypnosis and the efficacy of hypnotic analgesia and hopefully creating a new treatment modality for individuals suffering from pain syndromes such as fibromyalgia pain.

NCT ID: NCT02957110 Completed - Fibromyalgia Clinical Trials

Laughter Frequency and Fibromyalgia Symptoms

LAF
Start date: November 2016
Phase:
Study type: Observational

The purpose of this study is to investigate whether daily laughter frequency is associated with pain intensity and emotional state ratings in individuals who have fibromyalgia syndrome.

NCT ID: NCT02924259 Completed - Clinical trials for Myofascial Pain Syndromes

Does Self-myofascial Release With a Foam Roll Change Pressure Pain Thresholds in Lower Extremity Muscles

Start date: September 2016
Phase: N/A
Study type: Interventional

The purpose of this study was to examine the effects of a foam rolling intervention on pressure pain thresholds (PPT) of the ipsilateral antagonist and contralateral muscle groups. Through this research we sought to gather data to further develop the methodology for future studies of this intervention.

NCT ID: NCT02913976 Completed - Mobility Limitation Clinical Trials

Changes on Pain and Range of Motion by the Use of Kinesio Taping in Patients Diagnosed With Cervical Pain

Start date: October 2016
Phase: N/A
Study type: Interventional

The aim of this study is to demonstrate that the application of Kinesio Taping on a myofascial trigger point in the trapezius muscle able to cause a decrease of the pain and an increase of the cervical range of motion in patients diagnosed with cervical pain.

NCT ID: NCT02913963 Completed - Mobility Limitation Clinical Trials

Changes on Pain and Range of Motion by the Use of Kinesio Taping in Subjects With Myofascial Trigger Point

Start date: October 2016
Phase: N/A
Study type: Interventional

The aim of this study is to demonstrate that the application of Kinesio Taping on a myofascial trigger point in the trapezius muscle able to cause a decrease of the trigger point pain and an increase of the cervical range of motion in asymptomatic subjects

NCT ID: NCT02889991 Completed - Clinical trials for Myofascial Pain Syndromes

Evolution of Myofascial Pain, Post-dry Needling. Repair and Measuring With Elastography, of Myofascial Tissue.

INA-DMD
Start date: May 2, 2016
Phase: N/A
Study type: Interventional

This study evaluates the deep dry needling technique as a percutaneous technique included in the professional field of physiotherapy. The project quantifies a significant limit on the number of local twitch responses necessary for the favorable treatment of myofascial pain and analyzes the injury degree and/or the repair of myofascial tissue, with "Elastography".

NCT ID: NCT02881411 Completed - Clinical trials for Fibromyalgia Syndrome

Self Soft Tissue Therapy for Fibromyalgia Syndrome

Start date: July 2016
Phase: N/A
Study type: Interventional

The main aims of this preliminary research are to determine if combined self-soft tissue therapy (SSTT) alongside an established 6 week FMS Coping Skills Programme (FCSP) is a feasible and acceptable treatment approach for FMS. All participants on the six week FCSP will be randomly allocated to a control (FMS Coping Skills Programme) or intervention group (FMS Coping Skills Programme plus SSTT). All participants will be assessed for outcome measurements at the start of the feasibility study, at six weeks and three months after completion. This feasibility study hypothesis is that the SST approach will be acceptable to FMS patients and that the combined 6 week FCSP (hands off) and SSTT (hands on) will be beneficial. This feasibility study will inform a larger randomized controlled trial (RCT) on this combined treatment approach to FMS.