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McKenzie Exercises for Chronic Neck Pain: Stabilization vs. Non-Stabilization

Not Applicable
Completed
Conditions
Neck Pain
Cervical Pain
Registration Number
NCT05838794
Lead Sponsor
Ahram Canadian University
Brief Summary

PURPOSE: To compare the effects of mckenzie exercises plus stabilization exercise to those of mckenzie exercises alone on disability, pain, range of motion (ROM) in patients with nonspecific chronic neck pain (NSCNP).

BACKGROUND: Little is known about the efficacy of providing mckenzie exercises in addition to cervical and scapulothoracic stabilization exercises in people with NSCNP.

HYPOTHESES We hypothesize that there will be no significant effect of adding stabilization exercises to mckenzie exercises than mckenzie exercises alone in patients with NSCNP.

RESEARCH QUESTION: Is there a statistically significant effect of adding stabilization exercises to mckenzie exercises on outcomes of patients with NSCNP?

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
76
Inclusion Criteria
  1. Ages between 30 and 50 years
  2. Localized chronic neck pain without an exact etiology
  3. Absence of any arm pain or discomfort that could be replicated by neck mobility or irritant assessment
  4. Pain exists in the dorsal area, between two horizontal lines: the first line passes through 5) the lower half of the occipital area, and the second line runs through the spinous process of the first dorsal vertebra
Exclusion Criteria
  1. Neck pain caused by any other complications, such as a neoplasm, neurological diseases, or vascular diseases
  2. History of neck surgery or fracture
  3. Serious medical conditions that could affect participation in the study, such as cardiovascular disease, cancer, or autoimmune disorders
  4. Use of medication that could affect neck pain or exercise tolerance, such as opioids, muscle relaxants, or corticosteroids
  5. Participation in other treatments or interventions for neck pain during the study period
  6. Inability to understand or comply with study procedures or interventions, such as language barriers or cognitive impairment

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Pain intensity via Numeric pain rating scaleChanges in pain intensity at baseline and 6 weeks after end of treatment program.

The primary outcome measure will be pain intensity, assessed using the Numeric Pain Rating Scale (NPRS). The intervention will consist of a 4-week program of cervical and scapulothoracic stabilization exercises, performed 3 times a week under the supervision of an experienced physical therapist. Pain intensity will be measured at baseline and 6 weeks after the end of the treatment program.

Secondary Outcome Measures
NameTimeMethod
Cervical range of motionChanges in cervical range of motion at baseline and 6 weeks after end of treatment program.

Cervical range of motion will be assessed with the patient sitting comfortably on a chair, with both feet flat on the floor, hips and knees at 90° of flexion, and buttocks positioned against the back of the chair. A cervical range-of-motion (CROM) device will be placed on the top of the head, and the patient will be asked to move the head as far as possible without pain in a standard fashion: flexion, extension, right lateral flexion, left lateral flexion, right rotation, and left rotation. Three trials will be conducted for each direction of movement, and the mean values of the 3 trials will be recorded for analysis. The reliability of the CROM device in previous studies indicates intraclass correlation coefficients ranging from 0.66 to 0.94, suggesting that it is a valid and reliable method for measuring cervical range of motion.

Neck disability indexChanges in disability at baseline and 6 weeks after end of treatment program.

The Neck Disability Index (NDI) is a standardized questionnaire that assesses the degree of disability related to neck pain. It consists of 10 questions that evaluate the impact of neck pain on daily activities, such as personal care, lifting, reading, driving, and sleeping. Each question is rated on a scale from 0 to 5, with a total score ranging from 0 to 50. Higher scores indicate greater disability related to neck pain. The NDI is a widely used and validated tool for measuring neck pain-related disability and has been shown to be responsive to changes in disability over time. It is a recommended outcome measure in clinical trials and practice guidelines for patients with neck pain.

Trial Locations

Locations (1)

Outpatient clinic of faculty of physical therapy, Ahram Canadian University

🇪🇬

Al Ḩayy Ath Thāmin, Giza, Egypt

Outpatient clinic of faculty of physical therapy, Ahram Canadian University
🇪🇬Al Ḩayy Ath Thāmin, Giza, Egypt

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