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CompletedNCT03288688Updated Jun 12, 2018

Effect of an Exercise Program Designed for Orchestral Musicians

An interventional study of Exercise program and education in Musculoskeletal Disorder, sponsored by Laval University. Completed at 1 site in Canada. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-06-12.

Sponsored by Laval University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study 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.

02

Conditions studied

  • Musculoskeletal Disorder
03

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • 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)

Exclusion criteria

Exclusion Criteria:

  • 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
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    Exercise program and education

    An 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.

    Other: Exercise program and education

  • No intervention
    No intervention

    Participants in this group will be asked to continue their usual activities.

Interventions

  • OtherExercise program and education

    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.

05

What researchers measure

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

    Time frame: Baseline-11 weeks

Secondary outcomes

  1. The Nordic Musculoskeletal Questionnaire (NMQ)

    Self-report questionnaire on pain/symptom prevalence in the different regions of the body

    Time frame: Baseline-11 weeks

  2. Global Rating of Change

    Questionnaire designed to quantify participants' perceived improvement or deterioration over the course of the study

    Time frame: 11 weeks

06

Study locations

1 site
  • CIRRIS
    Quebec City, Quebec G1M 2S8, Canada
07

Registry details

Key details

Study ID
NCT03288688
Lead sponsor
Laval University
Responsible party
Jean-Sébastien Roy (PhD, Laval University) — Principal investigator
First posted
Sep 20, 2017
Start date
Sep 8, 2017
Primary completion
Nov 17, 2017
Completion
Nov 17, 2017
Last update
Jun 12, 2018

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2018. You cannot join it, but the record below documents what was studied.

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