- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01478464
Effect of Massage on Hamstring Muscle Soreness (IRMA)
June 27, 2013 updated by: Lars L. Andersen, National Research Centre for the Working Environment, Denmark
Danish: Integreret Motion på Arbejdspladsen (IRMA) English: Implementation of Exercise at the Workplace
Delayed onset muscular soreness peaks in 24-48 hours after unaccustomed strenuous physical exercise.
Therapists often provide manual massage with the hands to acutely relief the soreness.
Alternatives to manual hand massage can be useful for therapists.
Here the investigators examine the acute effect of a "massage roller" on DOMS in the hamstring muscles
Study Overview
Study Type
Interventional
Enrollment (Actual)
22
Phase
- Not Applicable
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
-
-
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Copenhagen, Denmark, 2100
- National Research Centre for the Working Environment
-
-
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
18 years to 67 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- working age adults
Exclusion Criteria:
- blood pressure above 160/100
- disease of the cervical spine
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: Prevention
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control group
Control group, does not receive any intervention
|
|
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Experimental: Massage group
Massage will be performed on the left or right hamstring muscle (randomized) for ten minutes with a massage roller.
The contralateral leg will not be massaged, but serve as a non-massaged control leg to assess possible cross-over effects from the massaged leg
|
The hamstring muscle will be massaged with a "massage roller" for ten minutes.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived soreness on a scale of 0-10
Time Frame: change from before to after massage (average of 0, 10, 30 and 60 min after)
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0: no soreness 10: worst imaginable soreness
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change from before to after massage (average of 0, 10, 30 and 60 min after)
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Pressure pain threshold (PPT) of the hamstring muscles
Time Frame: change from before to after massage (average of 0, 10, 30 and 60 min after)
|
change from before to after massage (average of 0, 10, 30 and 60 min after)
|
|
Hamstring range of motion
Time Frame: change from before to after massage (average of 0, 10, 30 and 60 min after)
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change from before to after massage (average of 0, 10, 30 and 60 min after)
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
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
December 1, 2011
Primary Completion (Actual)
November 1, 2012
Study Completion (Actual)
November 1, 2012
Study Registration Dates
First Submitted
November 18, 2011
First Submitted That Met QC Criteria
November 21, 2011
First Posted (Estimate)
November 23, 2011
Study Record Updates
Last Update Posted (Estimate)
June 28, 2013
Last Update Submitted That Met QC Criteria
June 27, 2013
Last Verified
June 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRMA03
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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