- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02420301
Effect of Self-administered Exercises on PRMD
Effects of Self-administered Exercises Based on Tuina Techniques on Musculoskeletal Disorders of Professional Orchestra Musicians
Objective: To study the effects of self-administered exercises based on tuina techniques on the pain intensity caused by playing related musculoskeletal disorders (PRMD) of professional orchestra musicians, using numeric visual scale (NVS).
Method: The investigators performed a prospective, controlled, single-blinded, randomized study with musicians suffering from PRMD. n= 69 musicians were randomly distributed into the experimental and into the control group. After an individual diagnostic assessment, specific tuina self-administered exercises were developed and taught to the participants. Musicians were instructed (educated) to repeat the exercises every day during 3 weeks. Pain intensity was measured by NVS before the intervention and after the 1st, 3rd, 5th, 10th, 15th and 20th days of self-exercising. The procedure was the same for the control group, however the Tuina exercises were executed in non-acupuncture points
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Professional orchestra musician presenting playing related musculoskeletal pain during at least 3 weeks
Exclusion Criteria:
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Exercises on real points
Self administered exercises were done in real treatment points
|
|
|
Placebo Comparator: Exercises on false points
Self administered exercises were done in false treatment points
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Verbal numeric scale
Time Frame: At the baseline
|
At the baseline
|
|
Verbal numeric scale
Time Frame: After one day
|
After one day
|
|
Verbal numeric scale
Time Frame: After 3 days
|
After 3 days
|
|
Verbal numeric scale
Time Frame: After 5 days
|
After 5 days
|
|
Verbal numeric scale
Time Frame: After 10 days
|
After 10 days
|
|
Verbal numeric scale
Time Frame: After 15 days
|
After 15 days
|
|
Verbal numeric scale
Time Frame: After 20 days
|
After 20 days
|
Collaborators and Investigators
Sponsor
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
Other Study ID Numbers
- claudiasousa_2
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