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Prevention of Musculoskeletal Injuries in Musicians

Prevention Programme for Cervicomandibular Musculoskeletal Injuries in Wind Musicians

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05277649
Enrollment
40
Registered
2022-03-14
Start date
2022-02-23
Completion date
2022-06-30
Last updated
2022-03-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical and Mandibular Pain and Disorders in Wind Players

Keywords

Musculoskeletal pain, Neck pain, Temporomandibular disorders, Posture, Musician

Brief summary

Musicians are a group with a high prevalence of musculoskeletal injuries. In particular, wind musicians, due to their playing requirements, are prone to suffer from cervical and mandibular alterations. For this reason, a specific exercise programme has been designed with the aim of analysing its effectiveness in improving these regions.

Detailed description

This study is a clinical trial with a control group whose participants are university music students specialising in wind instrument performance. The intervention of the participants in the Experimental Group consists of the individual performance of a specific programme of warm-up exercises prior to instrumental practice aimed at improving the mobility and strength of the cervical and mandibular regions, as well as a series of cool-down exercises after instrumental practice based on stretching the main muscles of both regions. Participants in the Control Group will continue their normal life without performing any specific exercise previously taught by the researchers. For the evaluation of the programme, an initial evaluation and a re-evaluation after 12 weeks will be carried out. In both, cervical and jaw mobility as well as body posture will be assessed. In addition, at the muscular level, the activity of the upper trapezius and masseter muscles will be assessed, and the pain threshold at trigger points will also be measured. The hypotheses are that by carrying out the exercise programme designed for wind musicians, an improvement in body posture, in the range of cervical and jaw mobility and in muscle activation will be achieved, as well as a decrease in the pain threshold. For the study of the results, an inferential statistical analysis of the data will be carried out using the Wilcoxon test for paired data or Student's t-test for repeated measures according to the sample characteristics in order to determine the effect of the exercise programme on the different variables of the experimental process. Correlation statistics will be used to establish the association between certain quantitative explanatory variables and ANOVA for categorical variables. The level of significance will be kept at p\<.05 and all calculations will be carried out using the SPSS 22.0 statistical programme.

Interventions

OTHERExercise programme

Performing a programme of warm-up and stretching exercises for the cervico-mandibular region aimed at improving mobility and muscle condition.

Sponsors

Margarita Pino Juste
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

The study consists of an experimental group, which will receive an intervention, and a control group, which will neither receive nor receive any intervention.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Woodwind or metal musicians * University students of music performance

Exclusion criteria

* Any surgical intervention in cervical spine, orofacial region or temporomandibular joint. * Analgesics or physiotherapeutic treatment in the last 24h. * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Cervical and orofacial painChange from baseline at 3 monthsVisual Analogic Scale. The pain VAS is a unidimensional measure of pain intensity, which has been widely used in diverse adult populations. The VAS is a straight horizontal line of fixed length, usually 100 mm. The ends are defined as the extreme limits of the parameter to be measured from 0 (no pain) to 10 (maximum pain). All the subjects will showed their pain level.
Head alignmentChange from baseline at 3 monthsHorizontal alignment of the head and shoulders using SAPO software. SAPO is a validated tool for head posture analysis.
Head positionChange from baseline at 3 monthsAssessment of head position by calculation of the craniovertebral angle, sagittal head angle and shoulder angle using SAPO software. SAPO is a validated tool for head posture analysis.
Cervical range of movementChange from baseline at 3 monthsEvaluation of cervical range of motion (flexion-extension, tilts and rotations) with Kinovea software. The Kinovea software is a validated tool to measure the movements of the cervical spine.
Temporomandibular range of movementChange from baseline at 3 monthsEvaluation of the maximum jaw opening with a vernier caliper. A vernier caliper is a validated tool to measure the MMO (maximum mouth opening).

Secondary

MeasureTime frameDescription
Masseter muscle activationChange from baseline at 3 monthsEMG assessment of resting and maximal contraction activation of the masseter muscle. Surface EMG is a validated tool for measuring muscle activation.
Trapezius muscle pain thresholdChange from baseline at 3 monthsPain threshold assessment at the trigger point of the upper trapezius muscle with a digital algometer. The digital algometer is a validated tool for assessing muscle pain threshold.
Masseter muscle pain thresholdChange from baseline at 3 monthsPain threshold assessment at the trigger point of the masseter muscle with a digital algometer. The digital algometer is a validated tool for assessing muscle pain threshold.
Trapezius muscle activationChange from baseline at 3 monthsEMG assessment of resting and maximal contraction activation of the trapezius muscle. Surface EMG is a validated tool for measuring muscle activation.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026