Eccentric Exercise in Patients With Non-Specific Neck Pain

April 12, 2023 updated by: Istinye University

Investigation of The Effect of Eccentric Muscle Training on Pain and Functionality in People With Non-Specific Neck Pain

Neck pain is one of the most frequently investigated and common musculoskeletal disorders that cause disability in the community.If neck pain is due to multifactorial etiology, it is defined as non-specific neck pain.Eccentric exercises are used to increase muscle strength and muscle mass.

Non-specific neck pain affects negatively and often leads to severe disability. Various rehabilitation techniques are available to reduce pain and disability and increase functional level.

This study aimed to compare the pain and functional status of eccentric exercise training and home program exercise groups of people with non-specific neck pain.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

It is known that exercise treatments are useful in strengthening neck muscles and controlling postural disorders in patients with neck pain, which is currently accepted. Eccentric exercises are used to increase muscle strength and muscle mass.

Home exercise and eccentric exercise training groups were included in a total of 24 sessions (8 weeks*3 days); home exercise program was applied to the individuals in the control group. Visual Analog Scale, Mc Gill Melzack Pain Assessment, Neck Disability Index, hand grip strength, and skin resistance assessments.

Study Type

Interventional

Enrollment (Actual)

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

      • Istanbul, Turkey, 34010
        • Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Istinye 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

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • diagnosed with Non-Specific neck pain by a physician
  • Having a complaint of non-specific neck pain for at least 3 months
  • Neck pain severity >40mm according to VAS
  • Voluntary participation of the individual in the study

Exclusion Criteria:

  • Radiculopathy and structural defect in the cervical region,
  • Surgical history on the cervical region,
  • Inflammatory disease,
  • Severe psychological illness,
  • Presence of infection in bone and soft tissue in the cervical spine,
  • Malignancy,
  • Advanced osteoporosis,
  • Having upper extremity pathologies,
  • Having a neurological disease that will prevent treatment
  • Having previously undergone cervical region and spine surgery
  • To be included in the physiotherapy program from the neck and back region in the last 6 months,
  • In case of administration of drugs such as NSAIDs, opioids in the last 24 hours

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
Active Comparator: Exercise
Eccentric muscle training for neck muscles
Eccentric Exercises for neck muscles.
No Intervention: Control
Home exercise program for neck muscles

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain Characteristics
Time Frame: before 8 weeks and end of the 8 weeks.
Pain frequency, duration
before 8 weeks and end of the 8 weeks.
Pain severity
Time Frame: before 8 weeks and end of the 8 weeks.
Visual analog scale-VAS
before 8 weeks and end of the 8 weeks.
Mcgill- Melzack Pain Questionnaire
Time Frame: before 8 weeks and end of the 8 weeks.the 24 session.
Mcgill- Melzack Pain Questionnaire
before 8 weeks and end of the 8 weeks.the 24 session.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Disability
Time Frame: before 8 weeks and end of the 8 weeks.
Neck Disability index
before 8 weeks and end of the 8 weeks.
Hand grip strength
Time Frame: before 8 weeks and end of the 8 weeks.
Digital Hand Dynamometer
before 8 weeks and end of the 8 weeks.
Skin resistance
Time Frame: before 8 weeks and end of the 8 weeks.
Digital Multimeter
before 8 weeks and end of the 8 weeks.

Collaborators and Investigators

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

September 15, 2021

Primary Completion (Actual)

September 30, 2022

Study Completion (Actual)

February 15, 2023

Study Registration Dates

First Submitted

February 15, 2023

First Submitted That Met QC Criteria

April 12, 2023

First Posted (Actual)

April 24, 2023

Study Record Updates

Last Update Posted (Actual)

April 24, 2023

Last Update Submitted That Met QC Criteria

April 12, 2023

Last Verified

April 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2021 / 16

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

no sharing of any participant's data

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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