NCT06352294

Brief 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). 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
45

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Apr 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 2, 2024

Completed
Same day until next milestone

Study Start

First participant enrolled

April 2, 2024

Completed
6 days until next milestone

First Posted

Study publicly available on registry

April 8, 2024

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 14, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 14, 2024

Completed
Last Updated

November 21, 2025

Status Verified

November 1, 2025

Enrollment Period

2 months

First QC Date

April 2, 2024

Last Update Submit

November 18, 2025

Conditions

Keywords

BalanceFunctionalityMyofascial relase

Outcome Measures

Primary Outcomes (2)

  • Pain severity

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

    6 weeks

  • Pressure pain threshold (PPT)

    Pressure pain threshold was measured with an algometer.

    6 weeks

Secondary Outcomes (4)

  • Balance

    6 weeks

  • Range of motion

    6 weeks

  • Neck Disability İndex

    6 weeks

  • DASH

    6 weeks

Study Arms (2)

Core stability training

ACTIVE COMPARATOR

A total of 18 sessions of core stabilization training will be given to the participants in 6 weeks.

Other: Core stability training

Basic stability training and myofascial relasing method

EXPERIMENTAL

Core stabilization training and myfacial relaxation application will be performed to the participants for 6 weeks and 18 sessions.

Other: Core stability training and myofascial relase

Interventions

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

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.

Basic stability training and myofascial relasing method

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • 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
  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kırşehir Ahi Evran Üniversitesi

Merkez, Kırşehir, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Neck Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

April 2, 2024

First Posted

April 8, 2024

Study Start

April 2, 2024

Primary Completion

June 14, 2024

Study Completion

June 14, 2024

Last Updated

November 21, 2025

Record last verified: 2025-11

Data Sharing

IPD Sharing
Will not share

Locations