Clinical Trials Logo

Shoulder Pain clinical trials

View clinical trials related to Shoulder Pain.

Filter by:

NCT ID: NCT05948007 Not yet recruiting - Post Operative Pain Clinical Trials

The Role of Neurofeedback Training and Pain Management in Post-operative Shoulder Rehabilitation

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

The primary aim is to compare the efficacy of neurofeedback training (NFT) and pain management protocol (PMP) in pain reduction, restoration of shoulder function, and improved cognitive performance as the post-operative rehabilitation protocols in shoulder pain patients.

NCT ID: NCT05946343 Recruiting - Shoulder Pain Clinical Trials

Rotator Cuff Tear Severity and Scapular and Rotator Cuff Muscle Activation Patterns

Start date: July 15, 2023
Phase:
Study type: Observational

Rotator cuff tears are common musculoskeletal injuries that can lead to altered scapular and rotator cuff muscle activation patterns and reduced function. This study aims to investigate the relationship between rotator cuff tear severity and scapular and rotator cuff muscle activation patterns. The primary objective of this study is to determine whether a relationship exists between the severity of rotator cuff tears and the activation patterns of scapular and rotator cuff muscles. Secondary objectives include: 1. Identifying differences in muscle activation patterns between varying tear sizes. 2. Evaluating the potential of these activation patterns as an indicator for the severity of rotator cuff tears. 3. Assessing the influence of muscle activation patterns on the functional capacity of the affected shoulder.

NCT ID: NCT05943340 Not yet recruiting - Shoulder Pain Clinical Trials

Shoulder Proprioceptive Training During Immobilization of the Wrist

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

The goal of this randomized clinical trial is to compare how a program of proprioceptive exercises for the shoulder could influence in pain, functionality, quality of life and shoulder muscle overload in people that are undergoing a immobilization period after a wrist fracture. The main questions it aims to answer are: - Study the relationship between shoulder muscle overload and shoulder pain. - Evaluate the effect of a proprioceptive program on pain and patient's satisfaction. Intervention will be: - Control group: participants of this group are not going to receive any protocol of exercises during the immobilization period. - Experimental group: participants of this group are going to receive a protocol of proprioceptive shoulder exercises to do during the immobilization period. Researchers will compare control and experimental group to see if a implantation of a proprioceptive program for the shoulder has benefits on pain, function, quality of life and muscle overload.

NCT ID: NCT05932186 Not yet recruiting - Shoulder Pain Clinical Trials

Upper Trunk Block Feasibility by Anesthesia Residents

Start date: July 15, 2023
Phase: Phase 4
Study type: Interventional

The study compares between the success rate of interscalene block and upper trunk block performed by anesthesia trainee for intra and postoperative analgesia during shoulder arthroscopy. The duration of performing the block, guidance intervention by the consultant and block failure will be recorded.

NCT ID: NCT05931185 Recruiting - Stroke Clinical Trials

Effects of Low Frequency TENS and Therapeutic Ultrasound in Post-stroke Shoulder Pain

Start date: November 11, 2022
Phase: N/A
Study type: Interventional

Brief Summary: Post-Stroke shoulder pain is a well-known complication and is responsible for the reduction in functional outcomes. A number of factors related to post-stroke shoulder pain including shoulder activity limitation, spasticity of shoulder muscles, and shoulder subluxation. Stroke patients may suffer from pain caused by the stroke itself (central post-stroke pain). Physical therapy plays an important role in the management of post-stroke shoulder pain. Different physical therapy techniques and modalities have been used in reducing pain and increasing functional outcomes in post-stroke shoulder pain patients. This study aims to provide a combined analysis of two modalities: low-frequency TENS and Therapeutic Ultrasound in terms of effects on pain and functional disability. This will be a randomized clinical trial to determine the analgesic effect of low-frequency transcutaneous electrical stimulation and therapeutic ultrasound on functional disability in post-stroke shoulder pain. The study will be conducted in accordance with ethical guidelines of Riphah International University and a convenience sampling technique will be used. Patients aged 65-84 years, with a history of pain of more than 4 weeks will be included in our study. Patients having a stroke with other neurological deficits, unstable cardiovascular diseases such as ventricular arrhythmias, and stroke patients with a history of diagnosed frozen shoulder will be excluded from the study. Subjects will be randomly allocated into three groups. Baseline assessment of pain and functional disability of patients will be done using outcome measuring tools and clinical tests. Group A will receive low-frequency TENS and therapeutic Ultrasound as a treatment, group B will receive therapeutic ultrasound and Group C will receive low-frequency TENS as a treatment. The duration of the study will be six weeks and patients will receive a total of 12 treatment sessions (3 sessions per week for 4 weeks and then follow-up will be done for the next 2 weeks) and the duration of each session will be of 20-25 minutes. After 12 sessions, a final assessment will be done and the results will be analyzed. Frequencies and mean standard deviation will be measured, and parametric and non-parametric tests will be applied.

NCT ID: NCT05917262 Recruiting - Pain, Postoperative Clinical Trials

Comparing Mindfulness-based Breath Training and Heart Rate Variability Biofeedback for Shoulder Surgery Patients in the Postoperative Pain.

Start date: November 13, 2023
Phase: N/A
Study type: Interventional

Although shoulder surgeries can effectively relieve pain intensity and restore shoulder function, some patients reported persistent post-operative pain at the 6-month post-surgery follow-up visit. This randomized study aims to determine the effectiveness of three different types of bio-psychosocial support to pre-operative shoulder surgery patients. This study will examine the differential effects of brief mindfulness-based breathing, heart rate variability biofeedback (HRV-BF), and cognitive behavioral pain psychoeducation for pre-operative patients.

NCT ID: NCT05904249 Completed - Shoulder Pain Clinical Trials

Telerehabilitation in Individuals With Rotator Cuff Tear

Start date: February 7, 2022
Phase: N/A
Study type: Interventional

The majority of patients presenting with shoulder pain are those with rotator cuff problems. Although telerehabilitation is a promising field in many areas, there is still limited high-quality research with strong evidence of its effectiveness for musculoskeletal problems. In this study, online rehabilitation and face-to-face rehabilitation will be compared in people with partial rotator cuff tears.

NCT ID: NCT05892250 Recruiting - Shoulder Pain Clinical Trials

Dynamic Humeral Centering Exercises in Subacromial Pain Syndrome

Start date: March 6, 2023
Phase: N/A
Study type: Interventional

Subacromial pain syndrome is one of the most common musculoskeletal health conditions, causing decreased of range of motion, loss of muscle strength and disability in the shoulder region. It has been proposed that dynamic humeral centering exercises could contribute to overcome these disorders, through the modification of the dimensions of the subacromial space, however, there is no consensus on its effectiveness nor direct variables that account for its efficacy. Therefore, the aim of this research is to determine the effects of a dynamic humeral centering exercise program on the functionality and disability of patients with subacromial pain syndrome.The effects of the dynamic humeral head exercises program, as well as the objective description of factors and variables associated with subacromial pain syndrome, will also allow rehabilitation science professionals to aim their interventions according to the knowledge of direct variables, which will allow objective follow-up of interventions on subacromial pain syndrome diagnosed patients.

NCT ID: NCT05883475 Completed - Stroke Clinical Trials

Effects of Hemiplegic Shoulder Pain

Start date: June 1, 2022
Phase:
Study type: Observational

The purposes of this study is to investigate the differences in upper extremity function, sleep quality, and functional independence between patients with and without hemiplegic shoulder pain (HSP). HSP is defined as musculoskeletal pain in the affected shoulders of individuals after stroke.Numerous studies have found an association between post-stroke shoulder pain and range of motion, sensory impairment, subluxation, spasticity, and complex regional pain syndrome. HSP is a problem that, starting from mild discomfort, leads to gradual functional impairment, ultimately resulting in increasing disability and decreased independence.In the literature, the relationship between HSP and upper extremity function, functional independence, and sleep quality has not been clarified.

NCT ID: NCT05882786 Not yet recruiting - Shoulder Pain Clinical Trials

Corticosteroid Injection Versus Tendon Dry Needling for Subacromial Impingement Syndrome

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

This randomized clinical trial aims to compare the efficacy of corticosteroid injection and tendon dry needling for the treatment of subacromial impingement syndrome.