What is robotic training studying for adhesive capsulitis of the shoulder?

Robotic training is being studied to see how it compares to conventional rehabilitation for patients with adhesive capsulitis, or frozen shoulder. The research aims to evaluate if robotics can improve shoulder function and pain management. This trial is sponsored by Mohammed V Souissi University and investigates new technology in physical therapy.

Who may be eligible for this adhesive capsulitis clinical trial?

Adults aged 18 and older with shoulder pain or movement limitations may be eligible. Both males and females can participate. People with certain conditions like recent shoulder surgery or neurological diseases are excluded. Please review eligibility criteria for more details.

Is there any cost to participate in this adhesive capsulitis clinical trial?

Study-related care, including the study therapy and all trial visits, is provided at no cost. However, personal travel expenses may vary and are not guaranteed to be covered.

Actively Recruiting

Phase Not Applicable

Age: 18Years +

All Genders

ID06766448

Robotic Training in the Management of Adhesive Capsulitis a Randomized Controlled Trial

Led by Mohammed V Souissi University · Updated on 2025-02-03

Participants Needed

Research Sites

12 weeks

Total Duration

AI-Summary

What this Trial Is About

Researchers are evaluating how robotic training compares to conventional rehabilitation for patients with adhesive capsulitis of the shoulder, also known as frozen shoulder. This study explores how new technologies like robotics and virtual reality might improve functional recovery and brain reorganization during rehabilitation. The trial aims to better understand the benefits of these approaches for restoring shoulder function and reducing pain. Participants are randomly assigned to one of two groups one group receives robotic training that includes continuous passive mobilization and therapy using the Armeo Spring device, while the other group undergoes standard rehabilitation sessions with a physiotherapist. Both treatments focus on improving shoulder movement and autonomy. The study does not use any masking or blinding methods. During the study, participants will have their shoulder function measured using the Shoulder Pain and Disability Index SPADI at multiple time points up to 12 months. Pain levels and active and passive range of motion will also be assessed regularly. This allows researchers to monitor progress and compare outcomes between the two rehabilitation methods. The total duration of participation may last about a year, with evaluations at 3 weeks, 6 weeks, 3 months, 6 months, 9 months, and 12 months.

CONDITIONS

Brief Title

Effectiveness of Instrumental Rehabilitation in Patients With Adhesive Capsulitis

Who Can Participate

Age: 18Years +

All Genders

Eligibility Criteria

You may qualify if you...

Patients over 18 years of age
Shoulder pain and/or movement limitation
Idiopathic adhesive capsulitis or adhesive capsulitis associated with confirmed systemic disease such as diabetes or dyslipidemia

You will not qualify if you...

Cognitive impairment
History of shoulder surgery
Fracture or dislocation of the shoulder
History of shoulder tendinopathy
History of inflammatory or degenerative shoulder disease
Infection
Neurological diseases such as Parkinson's disease, stroke, or multiple sclerosis
Manipulation under anesthesia, hydro dilation, platelet rich plasma, or hyaluronic acid infiltration within the last 6 months

Research Team

sara skalli, doctor

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