Validation of a Score for Shoulder Function Evaluation Based on Movement Analysis

NCT ID: NCT01281085

Last Updated: 2011-04-14

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 16 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2010-10-31
• Study Completion Date: 2011-04-30

Brief Summary

Questionnaires are frequently used to evaluate shoulder function in various diseases or after surgery. However, measurement of shoulder function is presently a controversial issue. Shoulder movement analysis based on embedded sensors could be a promising alternative to questionnaires. Some studies already demonstrated the relevance of this approach. It has also been demonstrated that a simple testing procedure including only two arm movements produces comparable results to more complicated testing procedures. However, more studies are needed to extensively establish if this simplified testing procedure provides a trustworthy evaluation of patient shoulder function and its evolution.

This study is a preliminary study which aims to develop a precise testing procedure which will be used in a future study aiming to evaluate measurement properties of a simple shoulder function test based on movement sensors.

Detailed Description

Background Measurement of shoulder function is a controversial issue. There is a great variety of measurement tools but none of them has been universally accepted. There is therefore a need to develop extensively validated and convenient measurement tools.

Embedded computerized movement analysis can potentially meet these requirements for measurement of shoulder function. Ambulatory measurement devices allow application in various clinical conditions, display adequate precision and accuracy, and are considerably more straightforward than laboratory-based systems.

Using a Physilog ® II embedded system, Coley (2007) developed a relatively simple score of shoulder function (P Score). The method is based on arm power measurement by three-dimensional accelerometers and gyroscopes during seven consecutive shoulder movements. It demonstrated reliability, responsiveness and criterion-based validity. However, additional knowledge and technological progress could now contribute to further simplification of the.

A secondary analysis of Coley's study data based on principal component analysis and multiple regressions highlighted that a procedure including only two selected movements produces comparable results to P Score. Moreover, the development of wireless systems considerably simplifies set up. Consequently, simpler but equivalent measurement procedure can now be considered.

However some important issues have to be clarified before an extensive validation study can be undertaken. The simplicity of the testing procedure allows test replication. However, the number of movement replications needed to obtain a reliable outcome is presently unknown. Relevance of testing procedure and study feasibility have also to be evaluated. A pilot study is needed to clarify these issues.

Aim The aim of this pilot study is to determine the number of movement replications needed to obtain a reliable result using a simplified cinematic shoulder measurement procedure as well as to evaluate testing procedure and study protocol.

Methods Measurement will be carried out with four groups of patients presenting with frequent shoulder conditions (rotator cuff condition, shoulder instability, diaphyseal or subcapital humerus fracture, frozen shoulder). Measurement procedure includes two consecutive measurements, alternatively conducted by two evaluators. Currently used functional questionnaires will be completed at both stages.

Statistical analysis will address outcome variability according to number of replications and reproducibility.

Conditions

Shoulder Pain

Study Design

• Study Time Perspective: PROSPECTIVE

Study Groups

No treatment

Shoulder conditions including rotator cuff condition treated conservatively, shoulder instability treated conservatively, diaphyseal humerus fracture or subcapital humerus fracture treated surgically and frozen shoulder

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Rotator cuff condition, conservative treatment indicated
• Shoulder instability, conservative treatment indicated
• Diaphyseal humerus fracture or subcapital humerus fracture treated surgically, at 6 weeks post surgery
• Frozen shoulder, conservative treatment indicated

• Any concomitant pain or condition involving upper limb
• Cervical spine condition involving upper limb pain or mobility restriction
• Insufficient French language level to understand patient information form, consent form or questionnaires

Exclusion Criteria

• Medical contraindication to execute movements required for score completion
• Tumor
• Neurological condition interfering with test

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Réseau d'études appliquées des pratiques de Santé de Réadapation (ré)insertion

UNKNOWN

Sponsor Role: collaborator

Haute Ecole de Santé Vaud

OTHER

Sponsor Role: lead

Responsible Party

HECVSanté, filière physiothérapie

Principal Investigators

Claude A. Pichonnaz, PT MSc

Role: PRINCIPAL_INVESTIGATOR

HECVSanté and CHUV-UNIL

Locations

Département de l'Appareil Locomoteur - CHUV

Lausanne, , Switzerland

Countries

Switzerland

References

Coley B, Jolles BM, Farron A, Bourgeois A, Nussbaumer F, Pichonnaz C, Aminian K. Outcome evaluation in shoulder surgery using 3D kinematics sensors. Gait Posture. 2007 Apr;25(4):523-32. doi: 10.1016/j.gaitpost.2006.06.016. Epub 2006 Aug 28.

Reference Type: BACKGROUND

PMID: 16934979 (View on PubMed)

Other Identifiers

SAGEX-24519

Identifier Type: -

Identifier Source: org_study_id