Effect of an Exercise Program Designed for Orchestral Musicians
1 other identifier
interventional
30
1 country
1
Brief Summary
This study is a randomized clinical trial evaluating the effect of an exercise program designed specifically for orchestral musicians on performance-related musculoskeletal problems (PRMPs). Professional and conservatory-level orchestral musicians will be recruited. Half of the subjects will participate in an 11-week home exercise program and attend three group exercise sessions and an educational presentation on injury prevention, while the other half of the subjects will receive no intervention, and continue their usual activities.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Sep 2017
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 8, 2017
CompletedFirst Submitted
Initial submission to the registry
September 18, 2017
CompletedFirst Posted
Study publicly available on registry
September 20, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 17, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
November 17, 2017
CompletedJune 12, 2018
June 1, 2018
2 months
September 18, 2017
June 8, 2018
Conditions
Outcome Measures
Primary Outcomes (1)
The Musculoskeletal Pain Intensity and Interference Questionnaire for professional orchestra Musicians (MPIIQM)
A biopsychosocial self-report questionnaire used to obtain demographic and occupational information and to document the intensity and impact of performance-related musculoskeletal pain/problems
Baseline-11 weeks
Secondary Outcomes (2)
The Nordic Musculoskeletal Questionnaire (NMQ)
Baseline-11 weeks
Global Rating of Change
11 weeks
Study Arms (2)
Exercise program and education
EXPERIMENTALAn exercise program in the form of home exercise videos will be given to the participants in this group. They will be asked to perform a minimum of two 35-minute exercise sessions per week, over a period of 11 weeks. They will also be required to attend three group exercise sessions, to confirm correct execution of the exercises. A short educational presentation on injury prevention will be offered at the beginning of the study, followed by three informative e-mails over the course of the study.
No intervention
NO INTERVENTIONParticipants in this group will be asked to continue their usual activities.
Interventions
The exercise program comprises warm-ups, exercises and cool-downs and aims to improve recruitment, strength and endurance of postural muscle groups that are key to the work of a musician. Basic activation exercises progress to dynamic and resisted exercises as well as functional musical movements. There is a series of six exercises of increasing difficulty for each of the following bodily regions: hips, back, neck, shoulders and abdominals. Topics to be discussed in the educational presentation and e-mails include healthy practice habits, activity dosage, the importance of physical activity, how the body adapts to workload and physical stressors, and instructions pertaining to the exercise program.
Eligibility Criteria
You may qualify if:
- professional or freelance orchestral musician, or tertiary-level full-time music student majoring in an orchestral instrument
- able to commit to performing exercises 2 times per week over an 11-week period
- medical condition permitting participation in an exercise program (ie. no serious heart or lung condition that may be exacerbated by physical exertion)
You may not qualify if:
- presence of musculoskeletal injuries definitively non-related to musical practice or performance
- fewer than 15 hours per week playing their instrument
- corticosteroid infiltration in the 6 weeks preceding recruitment
- prescribed anti-inflammatory drugs or neurontin in the 3 weeks preceding recruitment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Laval Universitylead
Study Sites (1)
CIRRIS
Québec, Quebec, G1M 2S8, Canada
MeSH Terms
Conditions
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PhD
Study Record Dates
First Submitted
September 18, 2017
First Posted
September 20, 2017
Study Start
September 8, 2017
Primary Completion
November 17, 2017
Study Completion
November 17, 2017
Last Updated
June 12, 2018
Record last verified: 2018-06