This is a randomised controlled study involving a group of 20 patients- 10 patients in a control group, 10 patients in treatment group. The treatment group consists of exercises with theraband for the shoulder and exercises of motor control of the scapula. The purpose of the study is to measure the effects of a pre-operative physiotherapy program for patients awaitng for rotator cuff surgery, The duration of the pilot project is 4 weeks.
This study is taken place in a genral hospital using the waiting list in the orthopedic surgery department- only patients awaitng for rotator cuff surgery are included. a randomised process of a block will be used. There will be 2 groups of patients an active comparator and no intervention. All patients at the beginning of the project and after 4 weks will have an evaluation on range of motion, strength, acromial humeral mesurement done by ultrasound and questionnaire on pain(DASH) and quality of life( WORC). At 8 weeks all patients will fill in the 2 questionnaires on DASH and WORC.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
20
exercise program on strengthening the rotator cuff muscles and motor control of the scapula
Hôpital Cite-de-la-Santé
Laval, Quebec, Canada
RECRUITINGWORC questionnaire
To evaluate function and quality of life at 0 weeks and 4 weeks
Time frame: 30 days
DASH questionnaire
To evaluate pain at 0 weeks and 4 weeks
Time frame: 30 days
Ultrasound measures
Mesurement distance of acromial-humerale distance at 0 and 4 weeks
Time frame: 30 days
range of motion
measurement of joint movement (active and passif range of motion) with goniometer at 0 and 4 week
Time frame: 30 days
strength
measurement of isometric strength with the Nicolas dynamometer at 0 week and 4 week.
Time frame: 30 days
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