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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01478451
Other study ID # IRMA02
Secondary ID
Status Completed
Phase N/A
First received October 28, 2011
Last updated February 27, 2012
Start date November 2011
Est. completion date January 2012

Study information

Verified date February 2012
Source National Research Centre for the Working Environment, Denmark
Contact n/a
Is FDA regulated No
Health authority Denmark: The Danish National Committee on Biomedical Research Ethics
Study type Interventional

Clinical Trial Summary

Many people experience pain, tenderness and soreness of joint and muscles, both in sport and working life. Pain killers can provide acute relief of pain, but may not be a feasible solution for all people. Here the investigators examine the acute effect of massage and exercise on induced muscle tenderness (delayed onset muscular soreness).


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date January 2012
Est. primary completion date January 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 67 Years
Eligibility Inclusion Criteria:

- working age adults

Exclusion Criteria:

- blood pressure above 160/100

- disease of the cervical spine

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
Exercise
Exercise will be performed for 10 minutes at the left or right trapezius (randomized)
Other:
Massage
massage will be provided for 10 minutes at the left or right trapezius (randomized)

Locations

Country Name City State
Denmark National Research Centre for the Working Environment Copenhagen

Sponsors (1)

Lead Sponsor Collaborator
National Research Centre for the Working Environment, Denmark

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Perceived tenderness of the trapezius muscle on a numerical rating scale of 0-10 Perceived tenderness where 0 is no tenderness and 10 is worst imaginable tenderness change from before to after the acute intervention (average of 0, 10, 20 and 60 min after the intervention) No
Primary Pressure pain threshold of the trapezius muscle change from before to after the acute intervention (average of 0, 10, 20 and 60 min after the intervention) No
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