Effect of Audible Manipulation Sound in Non-specific Cervicothoracic Pain

September 16, 2025 updated by: Ayça Aytar

Effect of Audible Manipulation Sound on Perceived Pain, Satisfaction and Disability in Non-specific Cervicothoracic Pain

The aim of this study is to investigate the effect of auditory manipulation sound on perceived pain, satisfaction and disability in patients with nonspecific cervicothoracic pain.İndividuals with nonspecific cervicothoracic pain will be included. the first group will be determined as those with an audible sound at the end of manipulation, and the second group will be determined as those without an audible sound at the end of manipulation. all evaluations and the patient's satisfaction level will be made before the application and 48 hours after the application.

Study Overview

Status

Active, not recruiting

Conditions

Detailed Description

Before the application, the pain intensity of the individuals will be assessed with a visual analog scale, and the level of disability will be assessed with the 'neck pain and disability index'. neck mobility will be measured with a cervical inclinometer and spinal region fascia mobility modified schober test, and also the thoracolumbar fascia flexibility will be recorded. .

Study Type

Interventional

Enrollment (Estimated)

38

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

    • Ankara
      • Ankara, Ankara, Turkey (Türkiye), 06790
        • Baskent University
    • Etimesgut
      • Ankara, Etimesgut, Turkey (Türkiye), 06790
        • Baskent 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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Clinical diagnosis of non-specific spinal pain
  • Must be able to do exercise by alone

Exclusion Criteria:

  • Clinical diagnosis of neurological problems (Alzheimer's, Demans)
  • Clinical diagnosis of deep vein thrombosis
  • Clinical diagnosis of systemic and uncontrolled metabolic diseases( Diabetes, Thyroid,hypertension)
  • Don't have pain while doing exercise

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: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: spinal manipulation
All participants will first receive a massage and then be manipulated with the spinal manipulation technique.
All participants will first receive a massage to relax the muscles and then be manipulated with a spinal manipulation technique.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Neck mobility
Time Frame: immediately before starting the application and 48 hours after the application
Neck mobility will be measured with a cervical inclinometer
immediately before starting the application and 48 hours after the application

Collaborators and Investigators

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

Sponsor

Investigators

  • Principal Investigator: nihan özünlü pekyavaş, Prof

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.

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)

April 10, 2025

Primary Completion (Actual)

May 20, 2025

Study Completion (Estimated)

September 30, 2025

Study Registration Dates

First Submitted

April 10, 2025

First Submitted That Met QC Criteria

April 10, 2025

First Posted (Actual)

April 18, 2025

Study Record Updates

Last Update Posted (Estimated)

September 19, 2025

Last Update Submitted That Met QC Criteria

September 16, 2025

Last Verified

May 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

We prefer to share our data and study design once they are published

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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