Effect of Cervical Stabilization and Oculomotor Exercises on Position Sense With Chronic Neck Pain

Not Applicable

• Conditions: Exercise Addiction; Chronic Neck Pain
• Interventions: Other: Classical Physiotherapy Program + Cervical Stabilization Exercises; Other: Classical Physiotherapy Program + Oculomotor Exercises; Other: Classical Physiotherapy Program

• Registration Number: NCT05083858
• Lead Sponsor: Eastern Mediterranean University

Brief Summary

The aim of this study is to compare the effectiveness of Cervical Stabilization and Oculomotor Exercises in addition to the classical physiotherapy on pain severity, cervical joint position sense, posture, cervical joint range of motion, strength and endurance of deep cervical flexor muscles, static and dynamic balance, neck awareness, functional disability and patient satisfaction in individuals with chronic neck pain. When the literature is examined, there is no study comparing the effectiveness of cervical stabilization and oculomotor exercises in individuals with chronic neck pain. However, it has also attracted our attention that a progressive and dynamic program was not followed in studies stating the oculomotor exercise program. In this sense, The study is important in terms of both comparing the effects of these 3 treatments and presenting a progressive and dynamic exercise protocol to the literature.

Detailed Description

The Participants included in the study will be divided into 3 groups. Participants in Group 1 will receive cervical stabilization exercises in addition to the classical physiotherapy program, individuals in Group 2 will receive oculomotor exercises in addition to the classical physiotherapy program, and only the classical physiotherapy program will be applied to group 3.

Transcutaneous Electrical Nerve Stimulation, hotpack, classical massage and stretching/posture exercises will be given to participants within the scope of the Classical Physiotherapy program. In addition to the classical physiotherapy program, the participants in the 1st and 2nd groups will be given exercises that gradually increase in difficulty level, 3 days a week, for a total of 8 weeks, under the control of a physiotherapist. Participants in the 3rd group will be given only classical physiotherapy. At the same time, stretching and posture exercises will be performed under the control of a physiotherapist.

Study Timeline

• Study Start: 2021-08-01
• Primary Completion: 2021-09-25
• Study First Submitted: 2021-09-27
• Status Verified: 2021-10
• Study First Submitted QC: 2021-10-07
• Last Update Submitted: 2021-10-07
• Study First Posted: 2021-10-19
• Last Update Posted: 2021-10-19
• Study Completion: 2022-07

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 72

Inclusion Criteria

• Men and women between the ages of 30-55,
• Neck pain for at least 3 months,
• Sedentary or non-regular exercise habit (3 days a week, less than 30 min of physical activity per day)
• According to the Numerical Pain Scale, the pain intensity is 4 cm and above

Exclusion Criteria

• • Has received any physiotherapy program due to neck or back pain in the last 6 months,

  • Congenital anomaly in the cervical region (such as Klippel Feil Syndrome)
  • Having structural scoliosis at any level of the vertebral column,
  • Acute or chronic neurological deficits (sensory and motor loss),
  • With vertebrobasillary artery failure,
  • Thoracic Outlet Syndrome,
  • Any vestibular problem,
  • With marked diplopia and oculomotor muscle insufficiency,
  • Having a cervical rib,
  • Having a history of fractures in the cervical vertebrae,
  • Colorblind,
  • Suffering from whiplash injury,
  • Those with serious rheumatic diseases such as Ankylosing Spondylitis, Rheumatoid Arthritis
  • Having undergone spine surgery from any region,
  • Tumor or spinal cord compression due to another reason,
  • Using any pain reliever drug other than simple analgesics.
  • Those who have problems related to the lumbar region such as lumbal stenosis, lumbar disc herniation

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Classical Physiotherapy Program + Cervical Stabilization Exercises	Classical Physiotherapy Program + Cervical Stabilization Exercises	In addition to classical physiotherapy, Cervical Stabilization Exercises will be applied to the individuals in the 1st group.
Classical Physiotherapy Program + Oculomotor Exercises	Classical Physiotherapy Program + Oculomotor Exercises	In addition to classical physiotherapy, Oculomotor Exercises will be applied to the individuals in the 2nd group.
Classical Physiotherapy Program	Classical Physiotherapy Program	Only the classical physiotherapy program will be applied to the individuals in 3rd group.

Primary Outcome Measures

Name	Time	Method
Cervical Joint Position Sense	Change from Cervical Joint Position Sense at the end of 8 weeks	Joint Position Sense of flexion-extension, right-left rotation and right-left lateral flexion movements of the cervical region will be evaluated. A laser marker will be used to perform the assessment. The target angle for cervical flexion, extension and right-left rotation joint position sense measurement is 30°, and 20° for right-left cervical lateral flexion. Measurements will be made with eyes open and eyes closed. Before the JPS evaluations, the method will be explained to the individuals in detail and a sufficient number of trials will be made before the tests. Considering that fatigue may affect the results, all individuals will be warned not to forcefully move their neck and back muscles before the measurement. In order to prevent proprioceptive input, they will be asked to come in comfortable clothes that do not wrap around the neck on the day of their evaluation.

Secondary Outcome Measures

Name	Time	Method
Pain Intensity	Change from Pain Intensity at the end of 8 weeks	Numerical Pain Scale will be used to determine the severity of neck pain at rest and during activity.An increase in the score means an increase in the severity of the patient's neck pain.
Static Balance	Change from Static Balance at the end of 8 weeks	Stork balance test will be used in the evaluation of static balance. While one side is standing on one foot, the individual places the other foot on the inside of the knee on which she/he is standing. She/he places his hands on the waist and, with the signal of the physiotherapist, raises the heel of the supporting leg from the ground. She/he tries to maintain this position as long as he can stand with his eyes open . After the trial, She/he will be told to take this position three times with his eyes open and the holding times will be recorded. The best score of the recorded times will be taken.
Patient Satisfaction	End of eight weeks	The Global Perceived Impact (GAE) questionnaire will be used to assess the extent to which individuals benefit from treatment after treatment. This questionnaire is used to evaluate the extent to which individuals benefit from treatment after treatment. Individuals are asked to rate between 1 (very much improved) and 9 (very much worsened) to the question 'How have your complaints changed compared to the time before your treatment?'. Scale scores were, in order, 1-very much improved, 2-very much improved, 3-moderately improved, 4-slightly improved, 5-unchanged, 6-slightly worsened, 7-moderately worsened, 8-very much worsened, 9-very much worsened. is in the form. Scoring will be done once at the end of the treatment.
Cervicothoracic angle	Change from Cervicothoracic angle at the end of 8 weeks	The posture of the cervical region will be evaluated by the lateral photographing method. Markers will be placed on specific anatomical points (C7, Tragus and T4) and the lateral projections of these points will be used for angular calculations. The photos transferred to the computer will be transferred to the paint program and the lines connecting the markers will be drawn. Cervicothoracic angle will be calculated using a computer program (Markus Bader-MB Software Solutions, Triangular Screen Ruler). Degree(°) is going to be record.
Cervical Joint Range of Motion	Change from Cervical Joint Range of Motion at the end of 8 weeks	Inclinometer (Baseline Bubble Inclinometer) will be used to evaluate the joint range of motion of the cervical region. Measurements of cervical flexion, extension and right-left lateral flexion will be made in sitting position, and right and left rotation measurements will be made in supine position.
Dynamic Balance	Change from Dynamic Balance at the end of 8 weeks	It will be evaluated using the Y balance test. The reach distance in the anterior, posteromedial and posterolateral transport directions will be recorded. People will be asked to reach the furthest point with the other foot while trying to maintain balance with the dominant foot on the wooden platform while the hands are on the waist. 3 repetitions of reaching out in 3 directions will be recorded.
Functional Disability	Change from Functional Disability at the end of 8 weeks	The Neck Disability Index (BDI) will be used to evaluate the functional disability of the neck. The questionnaire assesses how much neck pain associated with problems in the cervical region affects the individual in daily life and how much it interferes with the individual's daily work. The index consists of 10 items, 4 items evaluating subjective symptoms such as pain intensity, headache, concentration, sleep, and 6 items evaluating daily life activities such as personal care, lifting loads, reading, working life, driving, and leisure activities. Scoring is done between 0-5. The individual is asked to mark the answer that best fits him. If the total score obtained in the index is between 0-4, it is classified as no disability, between 5-14 as mild disability, between 15-24 as moderate disability, between 25-34 as severe disability and above 35 points as total disability.
Strength and Endurance of the Deep Cervical Flexor Muscles	Change from Strength and Endurance of the Deep Cervical Flexor Muscles at the end of 8 weeks	Craniocervical flexion test (CCFT) is used to evaluate the activation and static endurance of the deep flexor muscles of the cervical region. The test will be performed using Stabilizer Pressure Biofeedback (Chattanooga Stabilizer). The patient will be positioned in the supine position, with the cervical region in neutral position and the biofeedback pressure unit will be placed in the suboccipital space. The pressure cell will be inflated to 20 mmHg. Then, the individual will be instructed to perform a posterior tilt movement by increasing the pressure at 5 different levels (22, 24, 26, 28 and 30 mmHg.), Following the monitor of the device. After teaching the movement, the person will be asked to perform 10 contractions lasting 10 seconds at each level. The person will move to the next level after each successful attempt.
Neck Awareness	Change from Neck Awareness at the end of 8 weeks	The Fremantle Neck Awareness Questionnaire will be used to assess neck awareness. Fremantle Neck Awareness Questionnaire is a 9-item questionnaire that evaluates neck perception, attention and proprioceptive awareness of individuals with chronic neck pain. The first 3 questions of the questionnaire, which evaluates awareness in 4 dimensions, evaluate attention, the fourth and fifth questions evaluate proprioceptive perception, and the sixth, seventh and ninth questions evaluate how the neck is perceived as shape and size relative to its body. The eighth question was interpreted as 'negligence'. The questions of the Likert-type questionnaire are between 0 and 4 points, meaning 0=Never, 1=Rarely, 2=Sometimes, 3=Often, 4=Always. The total score is 36. A high score indicates decreased awareness of the neck.
Craniovertebral Angle	Change from Craniovertebral Angle at the end of 8 weeks	The posture of the cervical region will be evaluated by the lateral photographing method. Markers will be placed on specific anatomical points (C7, Tragus) and the lateral projections of these points will be used for angular calculations. The photos transferred to the computer will be transferred to the paint program and the lines connecting the markers will be drawn. Craniovertebral angle will be calculated using a computer program (Markus Bader-MB Software Solutions, Triangular Screen Ruler). Degree(°) is going to be record.

Trial Locations

Locations (1)

Eastern Mediterranean University; 🇨🇾 Famagusta, Cyprus