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Musculoskeletal Pain clinical trials

View clinical trials related to Musculoskeletal Pain.

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NCT ID: NCT01974791 Completed - Chronic Pain Clinical Trials

GET Living: Graded Exposure Treatment for Children and Adolescents With Chronic Pain

GET Living
Start date: October 2013
Phase: N/A
Study type: Interventional

The broad aim of the study is to implement and evaluate the efficacy of Graded Exposure Treatment (GET Living) to target elevated pain-related fears in children with chronic pain. Pain-related fear is an important psychological factor associated with poor outcomes in children suffering with chronic pain. To examine the efficacy of GET Living in addressing pain-related fears the investigators propose to use a sequential replicated randomized single-case experimental phase design with multiple measures. The specific aims are to 1) evaluate the effectiveness and acceptability of individually tailored GET Living for children with high pain-related fear and functional disability and 2) define anatomical and resting state connectivity patterns in the brains of children and adolescents with complex chronic pain prior to and after participation in GET Living.

NCT ID: NCT01956279 Completed - Fatigue Clinical Trials

Complementary Neurosteroid Intervention in Gulf War Illnesses (GWVI)

Start date: October 1, 2013
Phase: Phase 2
Study type: Interventional

This study will investigate the use of adjunctive pregnenolone for the following: 1. fatigue that has limited usual activity, 2. musculoskeletal pain involving 2 or more regions of the body and, 3. cognitive symptoms (memory, concentration, or attentional difficulties by self-report) in Veterans deployed to the Gulf War theatre of operations between 1990 and 1991.

NCT ID: NCT01944917 Recruiting - Clinical trials for Chronic Musculo-skeletal Pain

Effects of Pulsed Electromagnetic Field on Autonomic Function in Patients With Chronic Musculoskeletal Pain

Start date: August 2013
Phase: N/A
Study type: Observational [Patient Registry]

Previously it has been demonstrated that exposing the heart to electromagnetic field during exercise stress test improves the recovery following the stress test. This is explained by the effect of the electromagnetic field on the sympathetic activity of the heart. In the present study we would like to further investigate the effects of electromagnetic field on autonomic nervous system function in patients with chronic musculoskeletal pain that usually have high sympathetic activity. Each patient will be exposed to 20 minutes of electromagnetic field during which the autonomic nervous system function will be measured. In addition, patient tolerability to the exposed magnetic field will be investigated. We assume that short exposure to electromagnetic field would result in decreased sympathetic activity and therefore, on the long run, could be suggested as a therapeutic tool for such patients.

NCT ID: NCT01925508 Active, not recruiting - Clinical trials for Pre-eclampsia or Eclampsia With Pre-existing Hypertension

Evaluation of a Physical Therapy Protocol on Quality of Life Musculoskeletal Pain and Anxiety in Women With Preeclampsia

Start date: July 2012
Phase: N/A
Study type: Observational

The purpose of this study is to verify that the implementation of a protocol physiotherapy musculoskeletal pain and reduces anxiety and improves quality of life in patients hospitalized at the clinic of high-risk pregnancies at the Hospital das Clinicas of Ribeirao Preto, with a diagnosis of preeclampsia and chronic hypertension with superimposed preeclampsia. Where patients will be recruited, answered questionnaires before and after application of physiotherapy protocol.

NCT ID: NCT01827475 Completed - Pain Clinical Trials

Ibuprofen Versus Acetaminophen vs Their Combination in the Relief of Musculoskeletal Pain in the Emergency Setting

Start date: July 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether the combination of ibuprofen and acetaminophen, is more effective than either single agent alone in treating pain from acute musculoskeletal injuries in the emergency department.

NCT ID: NCT01813669 Completed - ADHD Clinical Trials

Integrative Coping Group for Children

ToPSY
Start date: October 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to examine whether an integrative group-based intervention will help children experiencing psychological and physical distress. Children, ages 10 to 12, will be recruited for participation in this therapeutic group. Eligible and consenting participants will be randomized to a wait-list control group or the group intervention. The group intervention will take place over a 12-week period, during which participants will attend a weekly coping skills group that integrates yoga-based practices (such as yoga poses, mindfulness, self-acceptance, breath work) with cognitive-behavioral principles (such as increasing awareness of thoughts and emotions).

NCT ID: NCT01784094 Completed - Low Back Pain Clinical Trials

Connective Tissue Motion Measure 2

Start date: January 2013
Phase: N/A
Study type: Observational

This study aims to compare the Connective Tissue Motion Measure (CTMM) in low back pain and no-low back pain subjects, evaluate the reliability of the CTMM, and examine the correlation of CTMM with low back pain symptoms, disability, and functional measures. The investigators hypothesize that CTMM will be reduced, on average, in low back pain subjects, that CTMM will be reliable with an intra-class correlation greater than 0.8, and CTMM will negatively correlate with low back pain symptoms, disability and functional measures.

NCT ID: NCT01570647 Completed - Clinical trials for Musculoskeletal Pain

Automated Connective Tissue Torque Sensor

StromaTorque
Start date: February 2012
Phase: N/A
Study type: Observational

The purpose of this study is to develop a measure - the needle torque test - capable of detecting connective tissue abnormalities associated with musculoskeletal disorders.

NCT ID: NCT01538745 Completed - Back Pain Clinical Trials

Low Dose Ketamine (LDK) Versus Morphine for Acute Pain Control in the Emergency Department

Start date: February 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the safety and effectiveness of intravenous low dose ketamine (LDK) to the industry standard of morphine (MOR) in regards to controlling acute pain in the emergency department. Both LDK and morphine have side effects. The amount and character of these side effects will be compared. Additionally, the degree of sedation or agitation will be specifically measured. The aim of this current study is to make this comparison and shift the evidence for LDK use from the anecdotal to the scientific.

NCT ID: NCT01528332 Completed - Chronic Pain Clinical Trials

Blue Light Device for Pain Therapy

PAINCT02
Start date: February 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if the Pain Relief Patch, which shines light of a limited wavelength on the painful area of the back, relieves chronic musculoskeletal back pain. At the same time, this study will gather information on side effects associated with use of the Pain Relief Patch. The study will compare the Pain Relief Patch to a patch that is similar in appearance, but which shines a different, presumed nontherapeutic, wavelength of light.