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Glenohumeral Re-centering During Closed Kinetic Chain for Shoulder Physiotherapy. A Prospective and Randomized Study. (SCAPULEO)

Primary Purpose

Subacromial Impingement of the Shoulder

Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Group C: physiotherapy protocol with Conventional physiotherapy.
Group S: physiotherapy protocol with Dynamic Humeral Centering.
Sponsored by
CHU de Reims
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Subacromial Impingement of the Shoulder focused on measuring Medical treatment, physiotherapy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Painful shoulder causes by tendinopathy of the rotator cuff (without full-thickness tear)
  • Diagnosis based on a MRI (dating less than 6 months)

Exclusion Criteria:

  • Tendinopathy of the rotator cuff with full-thickness tear
  • Stiffness of the shoulder (loss of more than 20° in passive external rotation or passive forward elevation)
  • Previous shoulder surgery (less than 12 months)
  • Previous subacromial injection (less than 6 months)
  • Context of worker's compensation claims

Sites / Locations

  • Chu de Reims

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

experimental group

control group

Arm Description

Dynamic Humeral Centering

Conventional physiotherapy

Outcomes

Primary Outcome Measures

Functional status of the shoulder
Functional status of the shoulder evaluated using the Constant & Murley Score

Secondary Outcome Measures

Functional status of the shoulder
Functional status of the shoulder evaluated using the Constant & Murley Score
Disabilities of the Arm, Shoulder and Hand score
Disabilities of the Arm, Shoulder and Hand score evaluated using the Quick-DASH (short form), self reported questionnaire (12 questions)
Disabilities of the Arm, Shoulder and Hand score
Disabilities of the Arm, Shoulder and Hand score evaluated using the Quick-DASH (short form), self reported questionnaire (12 questions)
Functional status of the shoulder
Functional status of the shoulder evaluated using Oxford Shoulder Score, self reported questionnaire (12 questions)
Functional status of the shoulder
Functional status of the shoulder evaluated using Oxford Shoulder Score, self reported questionnaire (12 questions)
pain
Shoulder pain evaluated using a visual analogic pain scale
pain
Shoulder pain evaluated using a visual analogic pain scale

Full Information

First Posted
August 11, 2016
Last Updated
May 12, 2021
Sponsor
CHU de Reims
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1. Study Identification

Unique Protocol Identification Number
NCT02874105
Brief Title
Glenohumeral Re-centering During Closed Kinetic Chain for Shoulder Physiotherapy. A Prospective and Randomized Study.
Acronym
SCAPULEO
Official Title
Glenohumeral Re-centering During Closed Kinetic Chain for Shoulder Physiotherapy. A Prospective and Randomized Study.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Terminated
Why Stopped
Difficulties for enrollment
Study Start Date
August 30, 2016 (Actual)
Primary Completion Date
May 21, 2019 (Actual)
Study Completion Date
February 26, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
CHU de Reims

4. Oversight

5. Study Description

Brief Summary
The rotator cuff tendinopathy is very common and associated with degenerative or traumatic changes of the rotator cuff and/or the sub-acromial bursa or the long head of the biceps. Lesions go of the simple tendinopathy without tear to the full-thickness tear of the cuff which means a loss of mobility or strength. The origin of this pathology remains controversial and many causes have been evoked (subacromial mechanical impingement, degenerative changes, muscle imbalance…). The clinical impairment is not always the same and varies from a painful shoulder with correct range of motion to a pseudoparalysis shoulder. The first treatment of the rotator cuff pathology is always non surgical and consists in relative resting, painkillers and/or non-steroidal anti-inflammatory drugs (NSAD) and physiotherapy. The aim of this management is to relieve pain and to restore the mobility and a good function of the shoulder. There is no consensus about the physiotherapy protocol for the treatment of the rotator cuff tendinopathy. In France, the most used physiotherapy protocol uses the strengthening of the muscles which stabilize the scapula (rhomboide muscles, trapezius and serratus anterior) and which lower the humerus (pectoralis major, latissimus dorsi and teres major). The aim of this approach is to augment the subacromial space in order to decrease the inflammation of the rotator cuff tendons and the associated pain. A technique of Dynamic Humeral Centering (DHC) uses a new method of glenohumeral centering in closed kinetic chain has been described ("3C Concept" for Centering in a Closed Chain). Dynamic humeral centring (DHC) is a modality of physiotherapy that aims to prevent subacromial impingement of rotator cuff tendons. In order to simplify and to improve its reliability, a special device called Scapuleo® has been developed. The aim of this device is to help the physiotherapist to realize simultaneously a subacromial decompression, a specific strengthening of the rotator cuff muscles and an optimal activation of the lower trapezius and the anterior serratus. Our hypothesis was that the DHC was not inferior to the conventional physiotherapy protocol for the medical treatment of the rotator cuff tendinopathy without full-thickness tear. We proposed a prospective and randomized study. All the patients treated in our department for simple tendinopathy of the rotator cuff or partial thickness tear were included in this study after signed consent. The physiotherapy protocol consists in 20 sessions of either "Conventional program" (Control group) or "Dynamic Humeral Centering" (Study group). The clinical evaluation included the range of motion measurement, Constant Score, Quick-DASH and Oxford Shoulder Score at 3 months and 6 months. Patients were blinded to the study hypothesis. The assessor of all outcomes was blinded to the interventions.
Detailed Description
Shoulder impingement accounts for 44 to 65% of shoulder complaints during physician visits. Shoulder impingement has been classified into two main categories: structural and functional. The structural impingement can be caused by narrowing of the subacromial space resulting from a reduction in the space due to bony growth or soft-tissue inflammation. The functional impingement or superior migration of the humeral head can be caused by weakness and/or muscle imbalance. It is possible that some subacromial impingement results from a combination of both structural and functional factors. Subacromial impingement occurs when the structures in the SAS (rotator cuff, biceps tendon long head, and subacromial bursa) become compressed and inflamed under the coracoacromial ligament. The suprasinatus tendon in particular is at highest risk for irritation and subsequent injury because it is the most likely to contact the acromion when the humerus is abducted to 90° and internally rotated 45°. The clinical impairment is not always the same and varies from a painful shoulder with correct range of motion to a pseudoparalysis shoulder. The first treatment of this subacromial impingement is always non surgical and consists in relative resting, painkillers and/or non-steroidal anti-inflammatory drugs (NSAD) and physiotherapy. The aim of this treatment is to relieve pain and to restore the mobility and a good function of the shoulder. There is no consensus about the physiotherapy protocol for the treatment of the shoulder impingement. In France, the most used physiotherapy protocol uses the strengthening of the muscles which stabilize the scapula (rhomboide muscles, trapezius and serratus anterior) and which lower the humerus (pectoralis major, latissimus dorsi and teres major). The aim of this approach is to augment the subacromial space in order to decrease the inflammation of the rotator cuff tendons and the associated pain. A technique of Dynamic Humeral Centering (DHC) uses a new method of glenohumeral centering in closed kinetic chain has been described ("3C Concept" for Centering in a Closed Chain). Dynamic humeral centring (DHC) is a modality of physiotherapy that aims to prevent subacromial impingement of rotator cuff tendons. In order to simplify and to improve its reliability, a special device called Scapuleo® has been developed. The aim of this device is to help the physiotherapist to realize simultaneously a subacromial decompression, a specific strengthening of the rotator cuff muscles and an optimal activation of the lower trapezius and the anterior serratus. Our hypothesis was that the DHC was not inferior to the conventional physiotherapy protocol for the medical treatment of the subacromial impingement. We proposed a prospective and randomized study. All the patients treated in our department for simple tendinopathy of the rotator cuff or partial thickness tear were included in this study after signed consent. The physiotherapy protocol consisted in 20 sessions of either "Conventional program" (Control group) or "Dynamic Humeral Centering" (Study group). The clinical evaluation included the range of motion measurement, Constant Score, Quick-DASH and Oxford Shoulder Score at 3 months and 6 months. Patients were blinded to the study hypothesis. The assessor of all outcomes was blinded to the interventions. The rhythm of the physiotherapy sessions was the same in both groups (3 sessions per week for 3 weeks, 2 sessions per week for 3 weeks and 1 session per week for 5 weeks). All patients received passive mobilization of the shoulder without pain and muscle stretching. Each physiotherapy session lasted 30 minutes and included massage or hot physiotherapy in case of VAS (visual analogic scale) of pain superior to 6/10.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Subacromial Impingement of the Shoulder
Keywords
Medical treatment, physiotherapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
experimental group
Arm Type
Experimental
Arm Description
Dynamic Humeral Centering
Arm Title
control group
Arm Type
Active Comparator
Arm Description
Conventional physiotherapy
Intervention Type
Other
Intervention Name(s)
Group C: physiotherapy protocol with Conventional physiotherapy.
Intervention Type
Other
Intervention Name(s)
Group S: physiotherapy protocol with Dynamic Humeral Centering.
Primary Outcome Measure Information:
Title
Functional status of the shoulder
Description
Functional status of the shoulder evaluated using the Constant & Murley Score
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Functional status of the shoulder
Description
Functional status of the shoulder evaluated using the Constant & Murley Score
Time Frame
3 months
Title
Disabilities of the Arm, Shoulder and Hand score
Description
Disabilities of the Arm, Shoulder and Hand score evaluated using the Quick-DASH (short form), self reported questionnaire (12 questions)
Time Frame
3 months
Title
Disabilities of the Arm, Shoulder and Hand score
Description
Disabilities of the Arm, Shoulder and Hand score evaluated using the Quick-DASH (short form), self reported questionnaire (12 questions)
Time Frame
6 months
Title
Functional status of the shoulder
Description
Functional status of the shoulder evaluated using Oxford Shoulder Score, self reported questionnaire (12 questions)
Time Frame
3 months
Title
Functional status of the shoulder
Description
Functional status of the shoulder evaluated using Oxford Shoulder Score, self reported questionnaire (12 questions)
Time Frame
6 months
Title
pain
Description
Shoulder pain evaluated using a visual analogic pain scale
Time Frame
3 months
Title
pain
Description
Shoulder pain evaluated using a visual analogic pain scale
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Painful shoulder causes by tendinopathy of the rotator cuff (without full-thickness tear) Diagnosis based on a MRI (dating less than 6 months) Exclusion Criteria: Tendinopathy of the rotator cuff with full-thickness tear Stiffness of the shoulder (loss of more than 20° in passive external rotation or passive forward elevation) Previous shoulder surgery (less than 12 months) Previous subacromial injection (less than 6 months) Context of worker's compensation claims
Facility Information:
Facility Name
Chu de Reims
City
Reims
ZIP/Postal Code
51092
Country
France

12. IPD Sharing Statement

Learn more about this trial

Glenohumeral Re-centering During Closed Kinetic Chain for Shoulder Physiotherapy. A Prospective and Randomized Study.

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