Effectiveness of Instrumental Rehabilitation in Patients With Adhesive Capsulitis

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMohammed V Souissi University

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • robotic training

    Other intervention

    continuous passive mobilization and robotic therapy on armeo sping

  • conventionnal rehabilitation

    Other intervention

    rehabilitation sessions with a physiotherapist

Treatment groups

70 Participants
are divided into 2 treatment groups
Group A: intervention groupExperimental treatment 1 intervention
Group B: control groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

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

Time frame
at 3 weeks, 6 weeks, 3 months, 6 months, 9 months and 12 months

Secondary outcomes

1

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.

Time frame
at 3 weeks, 6 weeks, 3 months, 6 months, 9 months and 12 months
2

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.

Time frame
at 3 weeks, 6 weeks, 3 months, 6 months, 9 months and 12 months

Other outcomes

Sponsors and contacts

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