Effectiveness of Pilates Exercises Applied to Violinists With Nonspecific Neck Pain

August 28, 2025 updated by: Dr. Öğr. Üyesi Ömer Şevgin, Uskudar University

Effectiveness of Pilates Exercises Applied to Violinists With Nonspecific Neck Pain : Randomized Controlled Trial

The aim of this study is to examine the effects of different Pilates exercises on violinists experiencing non-specific neck pain

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This study is planned as a randomized controlled study. Participants will be divided into two groups, mat pilates and reformer pilates, between the ages of 18-50. Participants will be asked to do the specified exercises for 6 weeks, 2 days a week and 45 minutes each session. Individuals with psychological and physical disabilities to do regular exercise will not be included in the study. The researcher will prepare a personal information form to collect the sociodemographic characteristics of the participants. A visual analog scale will be used to measure pain intensity and recovery process, a neck pain and disability scale to evaluate neck function and disability status, and a neck disability questionnaire to determine the effect of neck pain on daily life activities. These questionnaires will be repeated at the beginning and end of the study.

Study Type

Interventional

Enrollment (Actual)

30

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

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Individuals between the ages of 18-50
  • Individuals who play the violin with neck pain
  • Having received professional instrument training

Exclusion Criteria

  • Using medication
  • Having any pathology that prevents exercise
  • Having previously undergone upper extremity surgery

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: mat exercise group
mat execises
Other: mat pilates
Neck exercises Trunk stabilization exercises Shoulder exercises Posture exercises
Experimental: reformer exercise group
reformer exercises
Other: reformer pilates
Foodwork Swan Short Spin Long Stretch Keen Stretch Hug Tree Bridge Pulling Straps Short Box Abdominal Hundred Twist Star

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Neck Pain Disability Index Questionnaire
Time Frame: 8 weeks
The scale includes 10 titles. It includes pain sensitivity, heavy lifting, personal hygiene, reading, sleep, headache, concentration, work, driving, social activities. There are 6 answer options according to the severity of the limitation or pain. Scoring is between 0 and 5. The highest score is 50 and the least is 0. The neck disability level classification according to the total score is as follows 0-4: no restrictions 5-14: mild limitation 15-24: moderate limitation 25-34: severe limitation 34 and up: completely restricted
8 weeks
The Pittsburgh Sleep Quality Index (PSQI)
Time Frame: 8 weeks
Pittsburgh Sleep Quality Index; It evaluates sleep duration, sleep disturbance, sleep efficiency, subjective sleep quality, sleep medication use, daytime dysfunction, and sleep delay and consists of a total of 24 questions. 19 of them are self-report scales and 5 of them consist of questions to be answered by a friend or spouse. There are 7 components with 18 questions scored in the scale, and each component is evaluated between 0 and 3 points. The total score ranges from 0 to 21, and 5 or more is an indicator of "poor sleep quality"
8 weeks
Bournemouth Neck Pain Survey
Time Frame: 8 weeks
The survey consists of 7 questions. In addition to questions about pain and disability, it also includes questions about psychosocial issues. Each question is scored between 0 and 10. The highest score is 70, with a higher score indicating a higher level of disability. The content of the survey consists of variables that must be questioned for individuals with neck pain, such as pain severity, the effect of pain on daily life activities and social life, anxiety-depression level, kinesiophobia and coping with pain.
8 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Uskudar University

Investigators

  • Study Chair: Sümeyye Postacı, Uskudar university

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

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)

March 1, 2025

Primary Completion (Actual)

June 1, 2025

Study Completion (Actual)

August 10, 2025

Study Registration Dates

First Submitted

February 19, 2025

First Submitted That Met QC Criteria

February 19, 2025

First Posted (Actual)

February 25, 2025

Study Record Updates

Last Update Posted (Estimated)

September 5, 2025

Last Update Submitted That Met QC Criteria

August 28, 2025

Last Verified

August 1, 2025

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Uskudar21

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.

Clinical Trials on Occupational Diseases

Clinical Trials on mat pilates

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Mali

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

Subscribe