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Shoulder Pain clinical trials

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NCT ID: NCT03047434 Completed - Post Surgical Pain Clinical Trials

Characterization of PostOp Pain in Shoulder and Knee Arthroscopy

PurpleRain
Start date: November 9, 2016
Phase:
Study type: Observational

The purpose of this study is to describe the chronology of post operative pain in patients undergoing total knee arthroplasty and total hip arthroplasty. Further, within this population the predictive validity of the Defense and Veterans Pain Rating Scale will be assessed for persistent post surgical pain.

NCT ID: NCT03045432 Completed - Stroke Clinical Trials

Shoulder Passive Range of Motion and Positioning Exercise on Hemiplegic Stroke Patients

Start date: August 1, 2007
Phase: N/A
Study type: Interventional

Several factors associated with the hemiplegic shoulder pain after stroke includes rotator cuff injury, bicipital tendonitis, impingement, spasticity, limited external rotation of shoulder joint, adhesive capsulitis, shoulder subluxation, shoulder hand syndrome, and brachial/axillary neuropathy. In this study, the investigators aim to usie high frequency ultrasound to evaluate the relationship between stroke patients with poor shoulder motor function and shoulder tendon injury. Also, assumed that performing passive range of motion and positioning training might prevent tendon injury of shoulder and hemiplegic shoulder pain in either acute or chronic stage of stroke.

NCT ID: NCT03041727 Completed - Shoulder Pain Clinical Trials

Physiotherapist Approach to Shoulder's Diseases, Differences Between Fascial Manipulation and Standard Exercises

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

The study purpose is to compare the effects of Fascial Manipulation added to standard exercises protocol versus the simple exercises protocol.

NCT ID: NCT03000205 Completed - Clinical trials for Chronic Shoulder Pain

Effects of Hypertonic Dextrose Water Injection for Supraspinatus Tendinosis Patients

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

Using hypertonic dextrose water for chronic supraspinatus tendinosis and using ultrasound as assessment tool to evaluate the effect of intervention.

NCT ID: NCT02995941 Completed - Pain Clinical Trials

Shoulder Symptom Irritability Scale: A Single-Blinded Observational Study

SSIS
Start date: December 2016
Phase:
Study type: Observational

The purpose of this study is to examine the reliability and use of the shoulder symptom irritability classification system for the purposes of determining an appropriate treatment intensity to better help people with shoulder pain.

NCT ID: NCT02984228 Completed - Osteoarthritis Clinical Trials

Platelet-rich Plasma vs. Hyaluronic Acid for Glenohumeral Osteoarthritis

Start date: December 2014
Phase: Phase 4
Study type: Interventional

This study seeks to expand the current literature in demonstrating potentially efficacious, conservative treatments in the management of glenohumeral osteoarthritis (OA) and will compare ultrasound-guided injections of hyaluronic acid vs. platelet-rich plasma. We aim to obtain information measuring potential benefits of these interventions and to observe for any adverse events.

NCT ID: NCT02976974 Recruiting - Shoulder Pain Clinical Trials

Efficacy of Manual Therapy and Exercise in Patients With Shoulder Adhesive Capsulitis. A Randomized Clinical Trial.

MTEAC
Start date: July 30, 2016
Phase: N/A
Study type: Interventional

The efficacy of manual therapy and therapeutic exercise in patients suffering from adhesive capsulitis of the shoulder will be studied. Furthermore, different biomechanic and psychosocial factors will be measured with a nine month follow-up

NCT ID: NCT02971072 Completed - Pain Clinical Trials

Neurophysiology of Weakness and Exercise in Rotator Cuff Tendinopathy

Start date: July 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to examine deficits in activation and motor patterns, as well as central drive in patients with rotator cuff tendinopathy. There are three specific aims: (1) determine the effect of acute pain relief on rotator cuff muscle activation in patients with rotator cuff tendinopathy, (2) determine the effect of exercise on rotator cuff muscle activation in patients with rotator cuff tendinopathy, and (3) compare rotator cuff muscle activation between patients with rotator cuff tendinopathy and healthy controls.

NCT ID: NCT02960477 Not yet recruiting - Shoulder Pain Clinical Trials

Effectiveness of Pain Neuroscience Education vs Biomedical Education for Patients Undergoing Surgery for Shoulder Pain

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

BACKGROUND Shoulder pain is the third most common musculoskeletal disorder observed in primary care consultations after low back and neck pain. In the absence of successful outcome following a conservative intervention, shoulder surgery is the most common procedure conduct for a multitude of surgical indications, including rotator cuff tears, instability and stiffness. However, 22% of patients develop chronic shoulder pain (CSP) following shoulder surgery . The consequences of chronic or persistent postsurgical pain result in high socio-economic burden, not only in terms of suffering and reduced quality of life for the individual, but also, with considered the subsequent costs to healthcare and social services. Pain neuroscience education (PNE) has been shown as an effective therapeutic strategy for increasing knowledge and understanding about neurobiology, neurophysiology and processing pain, changing pain beliefs, improving patient's skills and encouraging to do physical and social activities in different chronic pain conditions. The primary aim of this study will be to evaluate whether perioperative PNE is more effective than classical biomedical education in reducing pain and disability in patients undergoing shoulder surgery. The secondary aim will be to analyse whether perioperative PNE is more effective than classical biomedical education in reducing postoperative healthcare costs and improving surgical experience in patients undergoing shoulder surgery .

NCT ID: NCT02954185 Terminated - Shoulder Pain Clinical Trials

Wellclub Shoulder Therapy Outcome Validation

Start date: November 1, 2016
Phase: N/A
Study type: Interventional

Preliminary evaluations have been completed and resulted in patients and therapist indicating positive outcomes through increased patient engagement, asynchronous communications (i.e. messaging) between therapists and patients, and objective assessment and monitoring of exercises performed by the patients. The investigator's hypothesis is that patients using the Wellclub device and application in addition to in-clinic physical therapy will be more compliant with their home exercise programs and have the same or better functional outcomes than patients with similar conditions who use in-clinic care only.