Chronic Shoulder Pain Treated by Pressures With the Thumbs on the Trigger Points

May 16, 2008 updated by: Guy Hains Chiropractor

Chronic Shoulder Pain of Myofascial Origin,a Randomised Clinical Trial Using Ischemic Compression Therapy.

The purpose of this study is to find the efficacy of treating the trigger points located around the shoulder in patients suffering from chronic shoulder pain.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

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

Interventional

Enrollment (Actual)

59

Phase

  • Phase 2
  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Quebec
      • Trois-Rivières, Quebec, Canada, G8Z3Y8
        • 2930 Cote Richelieu

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

30 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Guy Hains, DC, UQTR
  • Study Chair: Martin Descarreaux, DC, PHD, UQTR

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

September 1, 2003

Primary Completion (Actual)

December 1, 2006

Study Completion (Actual)

December 1, 2006

Study Registration Dates

First Submitted

May 15, 2008

First Submitted That Met QC Criteria

May 16, 2008

First Posted (Estimate)

May 19, 2008

Study Record Updates

Last Update Posted (Estimate)

May 19, 2008

Last Update Submitted That Met QC Criteria

May 16, 2008

Last Verified

May 1, 2008

More Information

Terms related to this study

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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