- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04801875
Cervical Pain and Exercise in Musicians
March 25, 2021 updated by: Serkan Usgu, Hasan Kalyoncu University
Effectiveness of the Selected Exercise Program on Non-specific Cervical Pain in Ney and Violin Performers
Exercise training that is one of the effective treatment methods for cervical pain, is crucial in developing mobility and stability.
Exercise training significantly reduces cervical pain as it advances postural alignment and neuromuscular coordination.
In many single group studies on cervical pain in violin performers, it has been reported that the stabilization exercises have favorable consequences on pain relief and postural correction.
But, there are no studies comparing ney and violin performers and analyzing the effectiveness of exercise training on non-specific cervical pain.
The aim of this study is to search the effects of selected exercise training on pain, disability, range of motion, flexibility, strength and quality of life in ney and violin performers with non-specific cervical pain.
Study Overview
Study Type
Interventional
Enrollment (Actual)
40
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Gaziantep, Turkey, 27144
- Hasan Kalyoncu University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Being professional musicians
- Using violin or ney musical instruments
- Had non-specific cervical pain during 3 months
Exclusion Criteria:
- Had cervical surgery in the last 3 months, discogenic pain, radiculopathy, neurological or systemic disorders,
- Missing exercise training session more than 2
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
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: Violin Performers
Violin performers received three 40-45 minute exercise sessions each week for eight weeks.
The selected exercise program designed to correct postural alignment.
|
The violin and ney groups performed a structured exercise training program 3 times a week for a total of 8 weeks.
Adherence to the exercise training program was checked using a follow-up schedule to ensure regular participation of the musicians.
The 8-week exercise training program was given with same physiotherapist under the same conditions.
The every exercise session consisted of warm-up (3-5 min), main exercise (30-35 min) and cooling periods (3-5 min).
The main exercise period was included ROM (10 min), stretching (5-7 min), isometric (5-10 min) and stabilization exercises (5 min).
|
|
Experimental: Ney Performers
Ney performers received three 40-45 minute exercise sessions each week for eight weeks.
The selected exercise program designed to correct postural alignment.
|
The violin and ney groups performed a structured exercise training program 3 times a week for a total of 8 weeks.
Adherence to the exercise training program was checked using a follow-up schedule to ensure regular participation of the musicians.
The 8-week exercise training program was given with same physiotherapist under the same conditions.
The every exercise session consisted of warm-up (3-5 min), main exercise (30-35 min) and cooling periods (3-5 min).
The main exercise period was included ROM (10 min), stretching (5-7 min), isometric (5-10 min) and stabilization exercises (5 min).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain intensity
Time Frame: 8 weeks
|
Visual Analog Scale (VAS) was used to measure the severity of pain.
In this scale, "0" indicates no pain, "10" indicates the highest value for perceived pain.
Participants were asked to illustrate the intensity of the pain they felt on a material with a horizontal line of 10 cm and was recorded as VAS score.
|
8 weeks
|
|
Functional Status
Time Frame: 8 weeks
|
The Northwick Park Neck Pain Questionnaire (NPQ) was used to specify functional status.
NPQ was developed to designate the level of disability in neck pain; It is a 9-item scale including neck pain severity, neck pain and sleep, numbness and tingling in the arms at night, duration of symptoms and complaints, weight-bearing, reading and watching television, work and housework, social activities, and driving.
It evaluates the severity, symptoms, duration of neck pain and disability in the activities specified in each item.
Each of them consists of 5 items and is scored between 0-4 points.
Neck pain total score consists of 36 points.
If the patients are not driving, the total score is calculated over 32 points.
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8 weeks
|
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Life Quality
Time Frame: 8 weeks
|
Quality of life was evaluated with the SF-36 scale.
The scale consists of 8 sub-parameters with a total of 36 items.
These sub-parameters are listed as; physical function, physical role limitation, pain, general health, energy (vitality), social function, emotional role limitation and mental health.
|
8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle Strength
Time Frame: 8 weeks
|
Muscle strength was measured with a digital muscle dynamometer (Jtech Commander Muscle Testing).
Anterior and middle part of deltoid, serratus anterior, upper and middle part of trapezius, cervical flexor and extensor muscles were measured.
|
8 weeks
|
|
Grip Strength
Time Frame: 8 weeks
|
The grip strength was measured with a hand dynamometer (Baseline, Hydraulic Hand Dynamometer).
Measurements were made in a sitting position, regardless of the right or left hand, with the elbow flexed at 90° and the arms in contact with the body without any abduction movement.
In this position, Individuals were asked to squeeze their hand with maximum force and measurements were repeated for other arm.
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8 weeks
|
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Range of Motion
Time Frame: 8 weeks
|
Cervical Flexion, extension, rotation and lateral flexion were measured by using a universal goniometer.
Head and trunk were held upright while participants were in a sitting position.
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8 weeks
|
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Spinal Mobility
Time Frame: 8 weeks
|
The jaw-sternum and jaw-wall distance were measured with a tape measure.
Participants was asked to stand upright in an anatomical position while leaning against the wall.
In this position, the distance of chin tip to wall and chin tip to the incisura jugularis were used.
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8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Chan C, Driscoll T, Ackermann B. Development of a specific exercise programme for professional orchestral musicians. Inj Prev. 2013 Aug;19(4):257-63. doi: 10.1136/injuryprev-2012-040608. Epub 2012 Dec 4.
- Kuo YL, Lee TH, Tsai YJ. Evaluation of a Cervical Stabilization Exercise Program for Pain, Disability, and Physical Impairments in University Violinists with Nonspecific Neck Pain. Int J Environ Res Public Health. 2020 Jul 28;17(15):5430. doi: 10.3390/ijerph17155430.
- Ackermann B, Driscoll T, Kenny DT. Musculoskeletal pain and injury in professional orchestral musicians in Australia. Med Probl Perform Art. 2012 Dec;27(4):181-7.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 2, 2018
Primary Completion (Actual)
June 2, 2019
Study Completion (Actual)
July 9, 2019
Study Registration Dates
First Submitted
March 13, 2021
First Submitted That Met QC Criteria
March 13, 2021
First Posted (Actual)
March 17, 2021
Study Record Updates
Last Update Posted (Actual)
March 30, 2021
Last Update Submitted That Met QC Criteria
March 25, 2021
Last Verified
March 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2017/14
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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