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Pain, Shoulder clinical trials

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NCT ID: NCT04538118 Completed - Rotator Cuff Tears Clinical Trials

Relationship of Patient-Specific Functional Scale With Shoulder Functions: A Prospective Study

Start date: January 5, 2019
Phase:
Study type: Observational [Patient Registry]

The aim of the study is to examine the relationship between the Patient- Specific Functional Scale (PSFS) and shoulder functions in the physiotherapy and rehabilitation program applied to patients with shoulder problems.

NCT ID: NCT04245657 Completed - Breast Cancer Clinical Trials

Factors Affecting Functionality in Breast Cancer Survivors

Start date: December 17, 2019
Phase:
Study type: Observational

Breast cancer is the most frequent cancer type in women globally. In conjunction with the new developments, breast cancer survival has increased therefore the management of long-term complications has gained importance. Breast cancer survivors can face the loss of muscle strength, increased fatigue and diminished physical function associated with treatment-related long term effects and psychological affection and thereby reduced quality of life. Upper extremity lymphedema or breast cancer-related lymphedema (BCRL) is one of the most prominent long term complications which affects breast cancer survivors in many ways after breast cancer surgery. It has been reported that breast cancer survivors with BCRL have the lower muscle strength and more activity limitations when compared to the ones free of BCRL. In BCRL, affected extremity has been found to 36% more weaker when compared to the unaffected side. Fatigue is one of the most prominent symptoms when considering cancer-related symptoms in cancer survivors. It has been stated that increased fatigue is correlated with increased activity limitation and deterioration in physical function. The hand-grip test which is frequently used in the assessment of decreased muscle function has been stated as a reliable and repeatable test in breast cancer survivors. In addition, this test is frequently applicable to assess mortality, physical and functional capacity, symptoms after surgery and to designate an exercise program. There are studies that investigate upper extremity function associated with hang-grip strength in breast cancer survivors. Yet, there is a lack of the objective result or conclusion of the BCRL effect on upper extremity function which is assessed with hang-grip strength when compared without BCRL. Therefore, this study is planned to investigate of cumulative effects of factors such as lymphedema severity, age, fatigue, body mass index, muscle strength, physical activity level, pain level, exercise benefits/barriers scale score on hand-grip strength related upper extremity functionality in breast cancer survivors.

NCT ID: NCT04233385 Recruiting - Breast Cancer Clinical Trials

Myofascial Massage for Pain and Immobility Following Breast Cancer Surgery

Start date: February 4, 2020
Phase: N/A
Study type: Interventional

About 25-50% of women who undergo breast cancer surgery develop persistent chest wall pain and shoulder mobility limitations following surgery. The pain and mobility limitations adversely affect quality of life, sleep, and body image. Unfortunately, current treatments for pain and mobility limitations have variable efficacy. Based on a review of relevant pre-, intra-, and post-operative factors, investigators reasoned that myofascial massage may address contributors to pain and mobility limitations following breast cancer surgery. Investigators propose a randomized controlled trial looking at myofascial massage compared to a light touch group to look at the effects on pain and immobility following breast cancer surgery.

NCT ID: NCT03752619 Active, not recruiting - Shoulder Pain Clinical Trials

Peripheral Nerve Stimulation(PNS) for Subacromial Impingement Syndrome(SIS)

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

Shoulder pain accounts for 16% of all musculoskeletal complaints in the healthy adult population. Subacromial impingement syndrome (SIS) is the most common cause of shoulder pain. Many patients with chronic pain from subacromial impingement syndrome (SIS) will fail treatment efforts and have longstanding pain. This project will evaluate the efficacy of a novel approach to treatment, percutaneous peripheral nerve stimulation, for participants with chronic shoulder pain due to subacromial impingement syndrome (SIS).

NCT ID: NCT03732456 Completed - Pain, Shoulder Clinical Trials

Post-operative Pain After Shoulder Surgery

Start date: July 19, 2018
Phase:
Study type: Observational

A prospective observational study conducted at the American University of Beirut Medical center that targets patients undergoing shoulder surgeries. It is conducted to to prospectively collect patient, surgery and anesthesia-related variables and perform correlation studies with postoperative pain severity, patients' satisfaction and analgesic consumption following shoulder surgery. In addition, identifying predictors for postoperative pain will contribute to adjust pain management protocols as per surgical and patients' factors.

NCT ID: NCT03373799 Completed - Rotator Cuff Tear Clinical Trials

Effectiveness of Video-Based Rehabilitation Program on Pain, Functionality and Quality of Life in the Treatment of Rotator Cuff Tears

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

The aim of this study was to investigate the efficacy of the video-based rehabilitation program on pain, functionality and quality of life in the conservative treatment of partial tears of the rotator cuff whether it was as successful as the physiotherapist-supervised rehabilitation program.

NCT ID: NCT03245320 Terminated - Clinical trials for Rheumatoid Arthritis

Clinical Evaluation of the TITAN™ Total Shoulder System

Start date: March 20, 2017
Phase:
Study type: Observational

A post market, non-randomized, multi-center, open-label,clinical study using survivorship to study the safety and efficacy of the Integra® TITAN™ Total Shoulder System 1.0 (TAS) when used for total shoulder arthroplasty.

NCT ID: NCT01785940 Completed - Pain, Shoulder Clinical Trials

Continuous Interscalene Block for Same Day Discharge Following Total Shoulder Arthroplasty

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

Total shoulder surgeries are associated with considerable postoperative pain which may prevent rehabilitation and early discharge from the hospital. Continuous interscalene blocks with home infusions are commonly performed for pain relief following total shoulder arthroplasties. We want to evaluate the time to readiness for discharge following interscalene blocks in patients undergoing total shoulder arthroplasties.