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Shoulder clinical trials

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NCT ID: NCT04513535 Completed - Muscle Strength Clinical Trials

Effects of Manual Therapy on Shoulder Function

Start date: February 7, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to directly compare the effects of four distinct interventions commonly used in the treatment of shoulder pathology on shoulder range of motion (ROM) and strength in asymptomatic shoulders: - grade III oscillatory anterior-posterior glenohumeral joint mobilizations - an internal rotation (IR) "sleeper" stretch - supine upper-thoracic manipulation - cervical spine manipulation

NCT ID: NCT04507854 Recruiting - Surgery Clinical Trials

Return to Performance Criteria Following Shoulder Instability Surgery in the Athlete.

Start date: September 15, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether certain criteria for returning to the field can be predictive of a return of the athlete to a level of performance similar to that of before his shoulder injury. In this context, these different criteria will be tested at 6 months in post-surgery while performance monitoring will be carried out at 12, 18 and 24 months.

NCT ID: NCT04312529 Recruiting - Muscle Strength Clinical Trials

Analysis of Shoulder Muscle Activity During Isokinetic Evaluation of Rotators

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

The objective of this study is to assess the impact of different positions of the glenohumeral joint on the maximum muscle contraction of different shoulder muscles. The muscles do not contract with the same intensity depending on the position of the arm in relation to the trunk. With the determination of this optimal position to activate the shoulder muscles as much as possible, we will be able to strengthen the patients during their revalidation.

NCT ID: NCT04307745 Completed - Primary Prevention Clinical Trials

Primary Prevention Habits for the Shoulder: Survey of the Sportsman's Entourage

Start date: June 5, 2020
Phase:
Study type: Observational [Patient Registry]

Purpose: To provide an update on the implementation of prevention among overhead athletes by their entourage. Materiel and method: This study will be conducted by the means of a questionnaire. The target population consisted of doctors, trainers, physical trainer and physiotherapist. The questionnaire will be validated by experts in each categorie and published on an online survey website

NCT ID: NCT04273633 Completed - Ultrasonography Clinical Trials

Ultrasound Supraspinatus Tendon Assessment After 448kilohertz Radiofrequency Stimulation in a Sporty Population.

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

448kilohertz capacitive resistive monopolar radiofrequency is a novel technique in physiotherapy and its usefulness and clinical relevance is still to be investigated at both clinical practice and also in performance. Current studies show promising results in different musculoskeletal disorders, however there no studies in the assessment of quality soft tissue in sporty population after the used of this technique.

NCT ID: NCT04196218 Not yet recruiting - Shoulder Clinical Trials

Driving After Shoulder Surgery

Start date: December 2025
Phase: N/A
Study type: Interventional

Patients undergoing a shoulder arthroplasty or rotator cuff repair will be enrolled in the study. Patients will be asked to undergo driving simulator assessments post-operatively in ATI Physical Therapy for up to 12 weeks after surgery in order to determine when it may be safe for them to return to driving. Additional assessments include patient-reported outcomes, range of motion, and strength measures, which are all standard of care. Study participation concludes when the patient passes the driving simulator test.

NCT ID: NCT03585491 Active, not recruiting - Clinical trials for Shoulder Dislocation

Shoulder Instability Trial Comparing Arthroscopic Stabilization Benefits Compared With Latarjet Procedure Evaluation

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

The primary objective of the pilot study is to assess the feasibility of a definitive trial to determine the effect of arthroscopic capsuloligamentous repair (Bankart + Remplissage) vs. coracoid transfer (Latarjet procedure) on recurrent dislocation rates and functional outcomes over a 24-month period.

NCT ID: NCT02631486 Completed - Rehabilitation Clinical Trials

Does Early Mobilisation Improve Outcomes After Rotator Cuff Repair?

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

Shoulder pain is among the most common musculoskeletal complaints, leading to high number of General Practioners consultations in the United Kingdom. On the top list of the disorders causing pain and dysfunction of shoulder is rotator cuff tears. The aetiology of rotator cuff tears is multifactorial and is likely to be a combination of age-related degenerative changes and trauma during life. It is present in approximately 25% of individuals in their 60s and 50% of individuals in their 80s and have been shown to start developing during the 40s. To recover functional status of this patients group, surgical repair is often recommended, but for optimal results the rehabilitation is of great importance and must be adequately planned. After surgery a period of movement restriction is followed, however, the optimal time of immobilisation is unknown. As a common practice, patients use a sling for six weeks and avoid any activities with the affected shoulder. This period is important to protect the tendon, allow good healing and to possibly prevent re-tear episodes. Although, the delayed motion may increase the risk of postoperative shoulder stiffness, muscle atrophy and potentially delay improvement of functionality. Based on the available evidence, it is difficult to make a clinical decision for a well-programmed rehabilitation regime and establish the most favourable postoperative time to start it. Moreover, it is not clear if early mobilisation will benefit more severe stages as published studies have methodological flaws that compromises the clinical decision for patients with higher commitments. The question whether early mobilisation application is beneficial is of high importance as the results will not just help improving patients quality of life, but also may reduce costs as further complication may be avoided.

NCT ID: NCT01544244 Terminated - Tendinopathy Clinical Trials

The Global Shoulder Concept (GSC) Method Versus Classic Physical Therapy for Shoulder Tendinitis

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

The primary objective of this study is to demonstrate the superiority of the CGE physical therapy protocol versus a standard physical therapy protocol of the shoulder by measuring the following after 1 month of physical therapy: the FI2S score including validated measures of pain, glenohumeral joint range of motion in the three planes, the ability to perform certain everyday activities and the strength of forward elevation measured with a dynamometer.

NCT ID: NCT01122732 Completed - Pain Clinical Trials

Comparison of Pain Relief After Non Stimulating Interscalene Catheter Placement vs Stimulating Catheter Placement in Total Shoulder Arthroplasty.

Start date: August 2010
Phase: N/A
Study type: Observational

1. Interscalene continuous catheter is a very effective way of controlling pain in total shoulder arthroplasty. To ensure proper placement, nerve stimulating catheter is quite often used. 2. Ultrasound can help proper placement of catheter without relying on nerve stimulation. 3. The plan of the study is to compare two techniques head to head to see if they are equally effective or one is better than others.