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Neck PainNCT06352294

Examining The Effects of Core Stabilization Exercises and Myofascial Release Technique in Individuals With Chronic Neck Pain: A Randomized Clinical Trial

A study testing Core stability training and Core stability training and myofascial relase in people with Neck Pain, run by Kirsehir Ahi Evran Universitesi at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Chronic neck pain is a musculoskeletal disorder that affects people frequently in life. Postural control is based on the process of correctly identifying and selectively focusing the incoming afferent input of the Central Nervous System (CNS). Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Neck Pain
What is being tested?
Core stability training and Core stability training and myofascial relase
Could I receive a placebo?
No, everyone receives an active treatment
How many people
45 participants
Where
1 siteTurkey (Türkiye)
Study dates
2 Apr 2024to 14 Jun 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Having neck pain that has been going on for at least three months
  • The mean pain intensity according to the Visual Analog Scale (GAS) is moderate [4-6.9 centimeters (cm)
  • December] or be at a severe (7 cm and above) level
  • To be between the ages of Dec 18-65
  • To be literate and to be a writer
  • Volunteering to participate in the study

Who cannot join

  • Having severe degenerative arthritis
  • Having a neurological finding due to spinal root compression (Positive upper limb stretching tests,cervical compression test)
  • To have a finding due to pressure of the spinal cord (Positive L'hermitte sign, Babinski sign) is
  • Having undergone cervical spine surgery
  • Having a cervical neck fracture and/or joint subluxation/dislocation
  • Having osteoporosis and/or neck pain due to a tumor
Show all 10Show fewer
  • Having a history of primary malignancy
  • Being pregnant
  • The title refers to neurological disease (Parkinson's, Multiple Sclerosis, etc.)
  • Having received physiotherapy and rehabilitation in the last three months

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Kırşehir Ahi Evran Üniversitesi

    Merkez, Kırşehir

Other trials in Turkey (Türkiye)

About this study

Official title: The Effects of Myofascial Relaxation Technique Applied Together With Core Stabilization Trainings on Balance, Pain, Joint Range of Motion and Functionality in Individuals With Chronic Neck Pain

Chronic neck pain is a musculoskeletal disorder that affects people frequently in life.

Postural control is based on the process of correctly identifying and selectively focusing the incoming afferent input of the Central Nervous System (CNS).

Read more

The main treatment options for people with neck pain include soft tissue and joint mobilizations, stabilization exercises for the neck, trunk and shoulder muscles, cervical Deckings, relaxation training, strengthening exercises and body awareness and posture training.

In this study, it was aimed to investigate the effects of myofascial relaxation on balance, pain, joint range of motion and functionality in individuals with chronic neck pain by dividing them into two groups in the form of core stabilization and core stabilization and myofascial relaxation.

The study included 45 people between the ages of 18 and 65. In two groups, the core stabilization group will be 22 people, and the core stabilization and myofascial relaxation group will be 23 people. The study period is planned as 6 weeks and 3 sessions per week.

Conditions
Neck Pain
Being tested
Core stability training, Core stability training and myofascial relase
Keywords
Balance, Functionality, Myofascial relase
Medical subject headings
Neck Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Core stability trainingOther

    Before starting core stabilization exercises, hotpack will be given for 15 minutes in the warm-up phase, TENS application, then craniocervical flexion training will be given. Core stabilization exercises consist of three stages: easy, medium and difficult

  • Core stability training and myofascial relaseOther

    Before starting core stabilization exercises, hotpack will be given for 15 minutes in the warm-up phase, TENS application, then craniocervical flexion training will be given. Core stabilization exercises consist of three stages: easy, medium and difficult. In addition, myofascial relaxation will be applied with roller bar along the superficial back line.

Study groups in NCT06352294
Study groupRoleWhat they receive
Core stability trainingActive comparatorA total of 18 sessions of core stabilization training will be given to the participants in 6 weeks.
Receives: Other: Core stability training
Basic stability training and myofascial relasing methodExperimentalCore stabilization training and myfacial relaxation application will be performed to the participants for 6 weeks and 18 sessions.
Receives: Other: Core stability training and myofascial relase

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pain severity

    Visual Analog Scale ( 0-10, higher means worse )

    Measured: 6 weeks

  2. Pressure pain threshold (PPT)

    Pressure pain threshold was measured with an algometer.

    Measured: 6 weeks

Secondary outcomes (4)
  1. Balance

    Measurements were made with a Biodex balance device. The scores obtained as a result of 3 measurements were averaged. As the score increases, the balance is considered to have worsened.

    Measured: 6 weeks

  2. Range of motion

    Movement skills of the neck area were recorded.

    Measured: 6 weeks

  3. Neck Disability İndex

    It is a disability level determination scale consisting of 10 questions for the person with neck pain.

    Measured: 6 weeks

  4. DASH

    It is a 30-question survey used to determine the level of functionality in patients suffering from upper extremity and neck pain. As the score increases, the level of disability increases.

    Measured: 6 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Apr 2024
  2. Study start2 Apr 2024
  3. Primary completion14 Jun 2024
  4. Study completion14 Jun 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
45 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06352294
Sponsor's protocol ID
MSDALAKCI
Status last verified
Nov 2025
First submitted
2 Apr 2024
Last updated
21 Nov 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Core stability training and Core stability training and myofascial relase in people with Neck Pain, run by Kirsehir Ahi Evran Universitesi at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 21 Nov 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pain severity (time frame: 6 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Nov 2025.

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