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NCT Number: NCT06766448

Effectiveness of Instrumental Rehabilitation in Patients With Adhesive Capsulitis

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

Recruiting

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Key information

Conditions

Adhesive Capsulitis of the Shoulder Bursitis Joint Diseases Musculoskeletal Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Faculty of medecine and pharmacy of rabat

Rabat, 10000, Morocco

Location status: Recruiting

Location contact

samia

CONTACT

[email protected]

sara skalli, doctor

PRINCIPAL_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

robotic training

Other

continuous passive mobilization and robotic therapy on armeo sping

conventionnal rehabilitation

Other

rehabilitation sessions with a physiotherapist

Primary outcomes

  1. 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

    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

  1. pain using a visual analogue scale

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

    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.

  2. Active and passive range of motion

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

    Active and passive range of motion is clinically assessed using a goniometer while standing. We measured abduction, extension and external rotation.

Study contacts

Contact information is provided by the study sponsor or research team.

sara skalli, doctor

CONTACT

[email protected]

+212661504251

Sponsors and collaborators

Lead sponsor

Mohammed V Souissi University

Other

Registry information

Official study title

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

Important dates

Study start
2021
Primary completion
2025
Study completion
2025
First posted
Jan 9, 2025
Registry last updated
Feb 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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