The purpose of this study is to evaluate the relation among shoulder kinematics during thoracohumeral, glenohumeral and scapulairthoracic elevations, performance of standardized ADL, Activitities od Daly Life, tasks and clinical outcome measures of…
ID
Source
Brief title
Condition
- Joint disorders
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The Constant Score, DASH-score, the NSST, Nederlandse Simpele Schouder Test,
and the Oxford Shoulder Score are already collected in a earlier time at the
out-patient polclinic.
The Fugl-Meyer Scores are collected during the investigation in the RCA,
Revalidatie Centrum Amsterdam.
Secondary outcome
There is no secundary endpoint.
Background summary
In situation where shoulder arthroplasty is necessary the totale shoulder
prosthesis offers a potentially beneficial surgical option.
Outcome studies thus far indicate that there is a tendency of placing a total
shoulder prosthesis in stead of a hemi-shoulder prosthesis ( see introduction
protocol ). This means that more total shoulder rehabiliation wil take place.
Mainly the glenohumeral motion of this prosthesis during movement, ADL-tasks
and rehabilitation is still unclear.
Study objective
The purpose of this study is to evaluate the relation among shoulder kinematics
during thoracohumeral, glenohumeral and scapulairthoracic elevations,
performance of standardized ADL, Activitities od Daly Life, tasks and clinical
outcome measures of shoulder function.
Study design
The patients are recruited from the OLVG hospital Amsterdam.
After their given informed consent, the patients are physical examined, with
includes testing tjemobility of the shoulder, as well as actively and
passively.
Then the range of motion is tested with an electromagnetic tracking device in a
non-invasive way, while the patient is performing three daily tasks. The final
step is an EMG study of the shoulder muscles recorded with surface electrodes
on the skin.
Study burden and risks
The patient takes place in an electromagnetic field, so the risk would be the
same as making a Magnetic Resonance Iamging scan, which is negletable.
Prinsengracht 769
1017 JZ AMSTERDAM
Nederland
Prinsengracht 769
1017 JZ AMSTERDAM
Nederland
Listed location countries
Age
Inclusion criteria
All patients from OLVG with total shoulderprosthesis and are compliant for the analysis, with minimal follow up of 6 months after the operation
Exclusion criteria
demention, painfull shoulder, pacemaker
Design
Recruitment
Medical products/devices used
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL32584.100.10 |