About this trial
The aim of this study is to evaluate the effectiveness of robotic training compared to conventional rehabilitation in patients with AC.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients >18 years of age
Shoulder pain and/or movement limitation
Idiopathic AC or associated with confirmed systemic disease (e.g., diabetes or dyslipidemia)
Disqualifiers
Cognitive impairment
History of surgery
Fracture or dislocation of the shoulder
History of shoulder tendinopathy
Trial design
Parallel
Treatments tested in this trial
robotic training
Other interventioncontinuous passive mobilization and robotic therapy on armeo sping
conventionnal rehabilitation
Other interventionrehabilitation sessions with a physiotherapist
Treatment groups
Trial outcomes
Primary outcomes
shoulder fonction using Shoulder Pain and Disability Index (SPADI)
It is a self-written questionnaire. It consists of twosubscales. The first assesses the importance of pain felt on five items. Pain scores range from 0 to 50. The second evaluates the difficulty of activities of daily living based on eight. Scores range from 0 to 80.questions
Secondary outcomes
pain using a visual analogue scale
It is a 100mm ruler that allows patients to rank their pain on a continuum from no pain to extreme pain. The patient places the indicator on a level that represents their current pain.
Active and passive range of motion
Active and passive range of motion is clinically assessed using a goniometer while standing. We measured abduction, extension and external rotation.
Sponsors and contacts
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