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Not yet recruiting NCT07476924

The Effect of Corrective Exercises in Individuals With Chronic Neck Pain

No phase Interventional Neck Pain

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Exercise, Posture education.
Who it may be relevant to
Registry conditions: Neck Pain. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Effect of Corrective Exercises on Pain, Functionality, and Dual-Task Gait in Individuals With Chronic Neck Pain

Overview

Our study will investigate the effects of corrective exercises on pain, functionality, and gait in individuals with chronic neck pain.

Detailed description

This study is a randomized controlled trial. The study population will consist of a total of 70 individuals with chronic neck pain, including students and staff from Dokuz Eylül University and İzmir Katip Çelebi University. Participants' socio-demographic characteristics will be recorded through face-to-face interviews. The 'BTS G-Walk' device will be used for gait assessment, the Neck Disability Index for functionality assessment, and the Verbal Rating Scale for pain intensity assessment. First, gait measurements will be taken. Gait assessment will be performed using the BTS G-Walk, and individuals will walk a distance of 10 meters. Individuals will first walk in normal walking patterns, and then in a dual-task walking pattern while carrying a tray. Exercises will be taught to participants individually in face-to-face sessions, and then they will be asked to perform them as home exercises three times a week for six weeks. Face-to-face meetings will be held with participants every two weeks via video conference to gather feedback on the exercises and make necessary updates. Patients will be randomly divided into two groups. The first group will receive corrective exercise training, while the second group, the control group, will receive behavioral modification and posture training in daily life. The effects of these two methods on pain, functionality, and gait in individuals with chronic neck pain will be compared.

Interventions

  • Other Exercise
    Corrective exercises will be taught to participants individually in face-to-face during the first session, and then they will be asked to perform them as home exercises 3 times a week for 6 weeks. Meetings will be held with participants every two weeks via video conference to obtain feedback on the exercises and make necessary updates.
  • Behavioral Posture education
    This is control group, they will receive behavioral changes and posture education in daily life

Primary outcome measures

  • Gait speed [Time frame: 6 weeks]
  • Cadence [Time frame: 6 weeks]
  • Stride length [Time frame: 6 weeks]
  • Step Length [Time frame: 6 weeks]
  • Pelvic symmetry [Time frame: 6 weeks]
Secondary outcome measures (2)
  • Neck Disability Index [Time frame: 6 weeks]
  • The Numeric Rating Scale [Time frame: 6 weeks]

Eligibility criteria

Inclusion criteria

  • Individuals aged 18 years and over
  • Individuals who have had neck pain for at least 3 months
  • Individuals with a Neck Disability Index (NDI) score of 10 or higher
  • Individuals who are able to understand the statements on the scale
  • Individuals who voluntarily agree to participate in the study after being informed about the study

Exclusion criteria

  • Individuals who have received physiotherapy for neck pain within the last 6 months
  • Individuals who have undergone neck surgery
  • Individuals with sensory loss
  • Individuals diagnosed with orthopedic, neurological, or vestibular disorders
  • Individuals with a history of trauma (whiplash)
  • Individuals diagnosed with or treated for cancer or osteoporosis

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Turkey (Türkiye) · 1 center
  • Izmir Katip Celebi University — Izmir

Identifiers

NCT: NCT07476924 · IRB-0092

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗