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Effects of Cervical Stabilization Exercise in Violinists With Chronic Neck Pain

Cervical Stabilization Exercises Improved Pain, Disability, and Physical Impairments in University Violinists With Nonspecific Neck Pain

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04051593
Enrollment
24
Registered
2019-08-09
Start date
2018-06-12
Completion date
2018-10-31
Last updated
2023-09-21

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

Conditions

Neck Pain

Keywords

cervical stabilization exercise

Brief summary

The purpose of this study is to examine the influence of a 6-week cervical stabilization exercise program in university violin players with chronic nonspecific neck pain.

Interventions

The participants followed instructional videos and performed the cervical stabilization exercise program at home for 20 minutes/day, 3 days/week, for 6 weeks.

Sponsors

National Cheng Kung University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 25 Years
Healthy volunteers
No

Inclusion criteria

* duration of playing the instrument longer than 5 years * practicing the violin more than 5 hours/week * constant neck pain for more than 3 months or at least 2 pain episodes in the last 3 months

Exclusion criteria

* previous surgery in the neck and shoulder regions * current participation in a structured exercises program * current treatment for neck and shoulder pain * red flags suggesting of cancer, infection, vascular insufficiency, and etc. during history taking * neurological symptoms of the upper extremities during screening tests (e.g. Spurling test and upper limb tension tests)

Design outcomes

Primary

MeasureTime frameDescription
Changes in self-reported neck pain: Numeric Rating ScalePre-test 1 (week 0), Pre-test 2 (week 4) and Post-test (week 10)Measured by the Numeric Rating Scale (min 0-max 10, better outcome 0 worst outcome 10)
Changes in neck disabilityPre-test 1 (week 0), Pre-test 2 (week 4) and Post-test (week 10)Measured by the Neck Disability Index (10-item questionnaire, each item scored from 0 to 5, result expressed as percentage, better outcome 0 worst outcome 100%)

Secondary

MeasureTime frameDescription
Changes in deep neck flexors functionPre-test 1 (week 0), Pre-test 2 (week 4) and Post-test (week 10)Measured by the craniocervical flexion test with a pressure biofeedback unit (higher pressure represents better outcome)
Changes in cervical muscle endurancePre-test 1 (week 0), Pre-test 2 (week 4) and Post-test (week 10)Measured using a stopwatch for the successful time holding the head in cervical flexion and extension positions (longer time represent better outcome)
Changes in cervical joint position sensePre-test 1 (week 0), Pre-test 2 (week 4) and Post-test (week 10)Measured by the cervcal joint reposition error with a laser pointer (short distance represent better outcome)
Changes in upper body posturePre-test 1 (week 0), Pre-test 2 (week 4) and Post-test (week 10)Evaluated by the photographic method

Countries

Taiwan

Outcome results

None listed

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