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Shoulder Pain clinical trials

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NCT ID: NCT04859387 Completed - Shoulder Pain Clinical Trials

Effectiveness of Pragmatic Shoulder Technique VS Traditional Physical Therapy

PSTVSTPT
Start date: April 15, 2020
Phase: N/A
Study type: Interventional

Isolated and combined effectiveness of pragmatic protocols on shoulder range of motion had been investigated and found effective in healthy participants. To our knowledge, there was insufficient literature to support the comparison between pragmatic and traditional protocols in the treatment of shoulder pathologies.

NCT ID: NCT04852640 Completed - Shoulder Pain Clinical Trials

Mitigating the Impact of Shoulder Movement Dysfunction; a Randomized Controlled Trial

Start date: September 1, 2021
Phase: N/A
Study type: Interventional

The purpose of the proposed work is to screen the effectiveness of an evidence-based, targeted, treatment intervention versus a non-specific, generalized, treatment intervention to treat symptomatic shoulder instability in collegiate swimmers. The results of the study will allow direct observation of treatment effects designed to mitigate the effects of symptomatic shoulder instability. These results will facilitate the optimization of future treatments and interventions.

NCT ID: NCT04833738 Completed - Pain, Shoulder Clinical Trials

Hyaluronic Acid, Corticosteroid and Electrotherapy in Subacromial Impingement Syndrome

Start date: September 11, 2013
Phase: N/A
Study type: Interventional

Background: Electrotherapy, corticosteroid, and hyaluronic acid have been used to treat subacromial impingement syndrome. However, we need to compare treatment options to provide the optimal results. This study aims to compare the effect of hyaluronic acid, corticosteroid, and electrotherapy in subacromial impingement syndrome. Design: Ninety five patients were randomised into three equal groups according to treatment types. Hyaluronic acid (20 mg/2ml, three times one week apart) or corticosteroid (triamcinolone acetonide, 40 mg/ml, single dose) treatments were applied as subacromial injections. Electrotherapy consisted of 14 sessions TENS (20 min.), hotpack (20 min.) and ultrasound (1.5watt/cm2, 1 MHz, 6 min.). Patients were evaluated before treatment, one and four weeks post end of treatment. Visual Analogue Scale (VAS), range of motion (ROM), and Shoulder Disability Questionnaire (SDQ) were used as outcome measures.

NCT ID: NCT04790071 Completed - Shoulder Pain Clinical Trials

Dry Needling Treatment in Hemiplegic Shoulder Pain

Start date: October 1, 2022
Phase: N/A
Study type: Interventional

To evaluate the efficacy of dry needling therapy on shoulder pain and upper extremity functions in hemiplegic patients.

NCT ID: NCT04768140 Completed - Clinical trials for Hemiplegic Shoulder Pain

Bobath Approach On Hemiplegic Shoulder Pain

BAHSP
Start date: August 10, 2019
Phase: N/A
Study type: Interventional

In this study, it is investigated that whether Bobath approach is superior to conventional physiotherapy in terms of improving hemiplegic shoulder pain, spasticity and upper extremity functionality in stroke patients.

NCT ID: NCT04755049 Completed - Shoulder Pain Clinical Trials

The Chinese Version of the American Shoulder and Elbow Surgeons Standardized Shoulder Assessment Form Questionnaire, Patient Self-report Section: A Cross-cultural Adaptation and Validation Study

Start date: March 1, 2020
Phase:
Study type: Observational

Background: The patient self-report section of the American Shoulder and Elbow Surgeons Standardized Shoulder Assessment Form (ASESp) is one of the most validated and reliable assessment tools. This study aimed to establish a validated Chinese version of ASESp (ASESp-CH). Methods: A clinical prospective study was performed. Following the guidelines of forward-backward translation and cross-cultural adaptation, a Chinese version of ASESp was established. Patients older than 18 years with shoulder disorders were included. Patients who could not complete test-retest questionnaires within the interval of 7-30 days and patients who received interventions were excluded. Intraclass correlation (ICC) was calculated for test- retest reliability, whereas internal consistency was determined by Cronbach value. Construct validity was evaluated by comparing the corresponding domains between the ASESp-CH and a validated Chinese version of 36-Item Short Form Health Survey (SF-36).

NCT ID: NCT04737980 Completed - Shoulder Pain Clinical Trials

Liposomal Bupivacaine Plus Bupivacaine Peripheral Nerve Blockade Versus Ropivacaine Plus Dexamethasone Peripheral Nerve Blockade for Arthroscopic Rotator Cuff Repair

Start date: July 18, 2019
Phase: Phase 4
Study type: Interventional

This study is a comparison of analgesia effect from peripheral nerve blockade (PNB) with liposomal bupivacaine combined with bupivacaine compared to PNB with ropivacaine combined with dexamethasone for arthroscopic rotator cuff repair.

NCT ID: NCT04724317 Completed - Shoulder Pain Clinical Trials

Ultrasound Guided Shoulder Intra-Articular Ozone Injection Versus Pulsed Radiofrequency Application for Shoulder Adhesive Capsulitis

Start date: January 5, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the efficacy of the ultrasound guided shoulder intra-articular Ozone injection versus pulsed radiofrequency application in patients with shoulder adhesive capsulitis. - Primary Outcome : - Pain score using visual analogue scale during rest (VASr) and movement (VASm). - Secondary Outcome : - Quality of life using Shoulder Pain and Disability Index (SPADI). It assesses the overall functionality of the shoulder joint. - Levels of serum ICAM -1, and serum high sensitive C-reactive protein (hs-CRP) are compared before and after treatment intervention.

NCT ID: NCT04692649 Completed - Shoulder Pain Clinical Trials

Comparison of Pragmatic Posterior Capsular Stretch and Crossbody Stretch on the Shoulder Mobility

Start date: January 5, 2021
Phase: N/A
Study type: Interventional

Various stretches are used to lengthen the posterior shoulder capsule. No study has reported the comparison of the pragmatic posterior capsular stretch and cross body stertch

NCT ID: NCT04669405 Completed - Hemiplegia Clinical Trials

High Intensity Laser Therapy in the Treatment of Hemiplegic Shoulder Pain

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

High intensity laser therapy (HILT) has been considered as a treatment option for shoulder pain. To our knowledge, the effectiveness of HILT in patients with hemiplegic shoulder pain (HSP) with partial thickness rotator cuff tear (PTRCT) is unknown. In this study, we intended to investigate the effectiveness of HILT on pain, disability, function and quality of life in patients with HSP accompanied by PTRCT.