- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00679887
Chronic Shoulder Pain Treated by Pressures With the Thumbs on the Trigger Points
Chronic Shoulder Pain of Myofascial Origin,a Randomised Clinical Trial Using Ischemic Compression Therapy.
Study Overview
Detailed Description
Chronic shoulder pain is a common condition which should be treated by surgery only wen conservative approaches have been tried. in the present trial the authors intend to find the effectiveness of treating the triggers points located in muscles, ligaments and tendons surrounding the shoulderin patients suffering from chronic shoulder pain.
The technique used in this trial is ischemic compression(thumb tip pressure) on the trigger points
Study Type
Enrollment (Actual)
Phase
- Phase 2
- Phase 1
Contacts and Locations
Study Locations
-
-
Quebec
-
Trois-Rivières, Quebec, Canada, G8Z3Y8
- 2930 Cote Richelieu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 30 to 60 years old.
- To have suffered from shoulder pain on a daly basis for at least 3 months
- Participants had to be able to raise the arm above ther head.
- They had accept to receive 15 chiropractic treatments without charge.
Exclusion Criteria:
- Past surgery to the arm.
- Injection to the shoulder in the month preceding the trial.
- A diagnosis of rheumatoid arthritis or any other systemic disorders affecting the joints.
- Shoulder pain from an herniated disc.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: A
Ischemic compression on trigger points located around the shoulder.
Active comparator.
Ischemic compression, 5 weeks
|
Active Comparator, ischemic compression, 3 times a week,5 weeks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Shoulder Pain and Disability Index questionnaire
Time Frame: At baseline, after 15 treatments ,30 days aftr the treatments and 6 months later
|
At baseline, after 15 treatments ,30 days aftr the treatments and 6 months later
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Pain visual analog scale
Time Frame: After 15 treatments, 30 days after the treatments and 6 months later.
|
After 15 treatments, 30 days after the treatments and 6 months later.
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Guy Hains, DC, UQTR
- Study Chair: Martin Descarreaux, DC, PHD, UQTR
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CER-05-102-07.05
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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