Effectiveness of Instrumental Rehabilitation in Patients With Adhesive Capsulitis
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: robotic training, conventionnal rehabilitation.
- Who it may be relevant to
- Registry conditions: Adhesive Capsulitis of the Shoulder. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Morocco
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Robotic Training in the Management of Adhesive Capsulitis: a Randomized Controlled Trial
Overview
The aim of this study is to evaluate the effectiveness of robotic training compared to conventional rehabilitation in patients with AC.
Detailed description
Nowadays, rehabilitation focuses on functional work during physiotherapy sessions to improve the patient's autonomy.
In the era of new technologies, robotics and virtual reality have shown great interest in functional rehabilitation and cortical reorganization.
Interventions
- Other robotic training
continuous passive mobilization and robotic therapy on armeo sping - Other conventionnal rehabilitation
rehabilitation sessions with a physiotherapist
Primary outcome measures
- shoulder fonction using Shoulder Pain and Disability Index (SPADI) [Time frame: at 3 weeks, 6 weeks, 3 months, 6 months, 9 months and 12 months]
Secondary outcome measures (2)
- pain using a visual analogue scale [Time frame: at 3 weeks, 6 weeks, 3 months, 6 months, 9 months and 12 months]
- Active and passive range of motion [Time frame: at 3 weeks, 6 weeks, 3 months, 6 months, 9 months and 12 months]
Eligibility criteria
Inclusion criteria
- Patients >18 years of age
- Shoulder pain and/or movement limitation
- Idiopathic AC or associated with confirmed systemic disease (e.g., diabetes or dyslipidemia)
Exclusion criteria
- Cognitive impairment
- History of surgery
- Fracture or dislocation of the shoulder
- History of shoulder tendinopathy
- History of inflammatory or degenerative disease
- Infection
- Neurological disease (Parkinson's disease, stroke, multiple sclerosis, neurological
- Manipulation under anesthesia, hydro dilation, platelet rich plasma or hyaluronic acid infiltration within the last 6 months
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Morocco · 1 center
- Faculty of medecine and pharmacy of rabat — Rabat
Identifiers
NCT: NCT06766448 · C63-20