Effectiveness of Instrumental Rehabilitation in Patients With Adhesive Capsulitis

NCT ID: NCT06766448

Last Updated: 2025-02-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-03-23

Study Completion Date

2025-04-30

Brief Summary

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The aim of this study is to evaluate the effectiveness of robotic training compared to conventional rehabilitation in patients with AC.

Detailed Description

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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.

Conditions

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Adhesive Capsulitis of the Shoulder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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intervention group

the intervention group will receive robotic training

Group Type EXPERIMENTAL

robotic training

Intervention Type OTHER

continuous passive mobilization and robotic therapy on armeo sping

control group

control group will receive conventionnal rehabilitation

Group Type ACTIVE_COMPARATOR

conventionnal rehabilitation

Intervention Type OTHER

rehabilitation sessions with a physiotherapist

Interventions

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robotic training

continuous passive mobilization and robotic therapy on armeo sping

Intervention Type OTHER

conventionnal rehabilitation

rehabilitation sessions with a physiotherapist

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Mohammed V Souissi University

OTHER

Sponsor Role lead

Responsible Party

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SARA SKALLI

assistant professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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samia karkouri, professor

Role: STUDY_CHAIR

Mohammed V Souissi University

Locations

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Faculty of medecine and pharmacy of rabat

Rabat, , Morocco

Site Status RECRUITING

Countries

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Morocco

Central Contacts

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sara skalli, doctor

Role: CONTACT

+212661504251

Facility Contacts

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samia

Role: primary

Other Identifiers

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C63-20

Identifier Type: -

Identifier Source: org_study_id

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