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Frozen Shoulder clinical trials

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NCT ID: NCT06129006 Not yet recruiting - Frozen Shoulder Clinical Trials

Ultrasound Guided Shoulder Anterior Capsular Infiltration Plus Hydrodilatation With Steroid Versus Hyalase in Patients With Frozen Shoulder

Start date: November 25, 2023
Phase: N/A
Study type: Interventional

To compare ultrasound-guided shoulder anterior capsular infiltration plus hydrodilatation with a steroid versus hyalase in patients with frozen shoulders

NCT ID: NCT06046430 Recruiting - Frozen Shoulder Clinical Trials

Investigation of Laterality and Sensory Acuity Abilities of Frozen Shoulder Patients

Start date: January 1, 2024
Phase:
Study type: Observational

The brain contains the body representation necessary for normal functioning, including goal-directed movements and behaviors. Body representation involves integrated sensory input and ideas about one's body. Both executed and imagined movements depend on the representation of the body in the cortical area. Laterilization is one of the motor imagery methods that requires activation of proprioceptive, somatosensory and premotor regions and enables the determination of pain-induced cortical changes. Another method to determine pain-related somatosensory changes is the two-point discrimination test. It is suggested that laterization and sensory acuity responses may change due to long-term pain and stiffness experienced in people with frozen shoulders. Therefore, the aim of this study is to investigate the laterization and sensory acuity abilities of patients with frozen shoulder.

NCT ID: NCT05993000 Completed - Exercise Clinical Trials

Assessment of Frozen Shoulder Treatment Using 432 Hertz Frequency Music: A Clinical Trial

Start date: May 29, 2021
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to determine the effect of listening to music during the treatment of frozen shoulder on pain, normal range of motion, functional activity status and quality of life.Upon recruitment, the subjects were randomly assigned to one of four treatment groups: Group 1 received Music + Mobilization + Exercise, Group 2 received Music + Exercise, Group 3 received Mobilization + Exercise, and Group 4 received Exercise only.

NCT ID: NCT05980572 Recruiting - Frozen Shoulder Clinical Trials

Effects of App-assisted Home Exercise Program in Patients With Frozen Shoulder

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

Abstract Introduction Frozen shoulder is a common musculoskeletal disorder with reported lifetime prevalence to be 2%~5% in the general population. Patients with frozen shoulders present with chronic pain and limited range of motion of affected shoulder and often cause an adverse impact on their daily activities and working ability. Shoulder exercises had been proven to be effective in treatment of frozen shoulders and the effects were even better after intraarticular corticosteroid injection. Strategies to enhance home exercise for patients with frozen shoulders are essential. Objective To compare the effects of home exercises delivered by a newly developed app named Defrozen app with that by convention home exercise for frozen shoulder patients after intra-articular corticosteroid injection. Methods and analysis This is a randomized, controlled, assessor-blinded clinical trial. Seventy-eight individuals diagnosed with frozen shoulders will be randomly divided into two groups. The primary outcome will be shoulder pain evaluated by 11-point numeric rating scale. The secondary outcomes will include shoulder passive range of motion (measured with a universal goniometer), , Oxford shoulder score and Disabilities of the arm, shoulder and hand questionnaire. Feasibility of the app includes including Technology Acceptance Model (TAM-2), System Usability Scale (SUS) and Usability, Satisfaction and Ease of Use (USE) questionnaire . The treatment will be conducted for 6 months (Defrozen app home exercise x conventional home exercise by instructions from printed pamphlets).All participants will receive outcome measurements assessment prior to randomization , 4 weeks , 12 weeks after injections interventions. Feasibility will be evaluated 4 weeks after intervention in the Defrozen app group. Ethics and dissemination The study protocol was approved by the Institutional Review Board. The findings of the trial will be disseminated through peer-reviewed journals and scientific conferences.

NCT ID: NCT05979974 Recruiting - Frozen Shoulder Clinical Trials

High Energy Density Pulse Electromagnetic Field for Patients With Frozen Shoulder

Start date: October 31, 2023
Phase: N/A
Study type: Interventional

The aim of our study is to investigate the efficacy of high energy density pulse electromagnetic field for patients with frozen shoulder

NCT ID: NCT05956171 Not yet recruiting - Shoulder Pain Clinical Trials

The Effects of Two Different Treatment Protocols on Shoulder Function, Quality of Life, and Ultrasound Parameters in Patients With Frozen Shoulder

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

The goal of this interventional study is to compare the outcomes of two different injection aprroaches in patients with frozen shoulder. The main questions it aims to answer are: - Is hydrodilatation better than intraarticular corticosteroid injection? - Is there any prognostic factors that will help clinicians guide their decision making when choosing between these two treatments? Participans will receive an injection(cortcosteroid and local anesthetics alone or with hydrodilatation-corticosteroid and local anesthetics plus sterile saline solution) and then they will follow a rehabilitation program.

NCT ID: NCT05931666 Completed - Frozen Shoulder Clinical Trials

Gong v/s Kaltenborn Mobilization in Frozen Shoulder

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

The aim of this research is to determine the effects of Gong mobilization and Kaltenborn mobilization in patients of frozen shoulder. This is a Randomized clinical trial. The sample size is 40. The subjects are divided in two groups, with 20 subjects in Group A and 20 subjects in Group B. Study duration is of 6 months. Sampling technique applied is Nonprobability Purposive Sampling. Both males and females of aged 40-65 years with Stage-II frozen shoulder are included. Tools used in the study are Visual Analogue Scale (VAS), Goniometer, and SPADI (Shoulder pain and disability index) questionnaire.

NCT ID: NCT05897866 Completed - Rotator Cuff Tear Clinical Trials

Sayed Issa's Hybrid Shoulder Arthroscopic-Open Surgical Management (HSSM)

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

Sayed Issa's Hybrid Shoulder Arthroscopic-Open Surgical Management (HSSM) is a limited lateral approach to the shoulder arthroscopically guided. Which achieves less surgical trauma and smaller surgical incision than even in Mini Lateral Shoulder Approach (MLSA).

NCT ID: NCT05811533 Completed - Frozen Shoulder Clinical Trials

Comparison of Spencer's Muscle Energy Technique and Post-facilitation Stretch in Patients With Adhesive Capsulitis

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

Adhesive capsulitis is one of the most common problems of the upper limb. Adhesive capsulitis (AC) and frozen shoulder syndrome (FSS) are two terms that have been used to describe a painful and stiff shoulder. Conservative treatment includes transcutaneous electrical nerve stimulation (TENS), Ultrasound, LASER, Range of Motion, stretching and strengthening exercises, patient education, and home exercises. Manual therapy includes mobilization, Spencer's Muscle Energy Technique and Mobilization With Movement.

NCT ID: NCT05466435 Not yet recruiting - Frozen Shoulder Clinical Trials

Heavy Slow Resistance Training in Adults With Frozen Shoulder

HSRFSRCT
Start date: August 2022
Phase: N/A
Study type: Interventional

The aim of the study is to evaluate the efficacy of Heavy Slow Resistance exercise in patients diagnosed with frozen shoulder using randomized controlled trial design