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Eye-Cervical Re-education Versus Motor Imagery Therapy on Proprioception in Chronic Mechanical Neck Pain (MNP)

Primary Purpose

Neck Pain

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
eye cervical re-education
motor imagery therapy
conventional physical therapy
Sponsored by
Cairo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neck Pain focused on measuring Eye-Cervical Re-education, Motor Imagery Therapy, neck pain

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age will range from 18 to 70 years Patients of both sexes. Neck pain diagnosed by physician greater than 3 months in duration. Active or latent myofascial trigger points (MTrPs) in at least one of the following muscles: upper trapezius, levator scapulae, or splenius capitis. Both active and latent MTrPs were considered because latent MTrPs have been associated with the development of sensory motor dysfunction and may contribute to different chronic musculoskeletal pain disorders Exclusion Criteria: Dizziness syndrome. Post-traumatic as whiplash Neurological, infectious, or tumor cervical pain. Pregnant women. Patients having speech and understanding problems. Past history of neck surgery Dizziness syndrome. Post-traumatic as whiplash. Neurological, infectious, or tumor cervical pain. Pregnant women. Patients having speech and understanding problems. Past history of neck surgery .

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Experimental

    Active Comparator

    Arm Label

    eye cervical re-education

    motor imagery therapy

    conventional physical therapy

    Arm Description

    patients will receive eye cervical re-education three times a week for four weeks

    patients will receive motor imagery therapy three times a week for four weeks

    patients will receive conventional physical therapy three times a week for four weeks

    Outcomes

    Primary Outcome Measures

    joint position error
    The Cervical Joint Position Error (JPE) Test is a measurement tool used to clinically assess an individual's cervicocephalic proprioception ability. Cervicocephalic proprioception describes one's sense of position of their head and neck in space. The Cervical JPE Test measures the ability of a blindfolded patient to accurately relocate their head position back to a predetermined neutral point after cervical joint movement. The test is most commonly performed with head movement in the transverse and sagittal planes by cervical range of motion device (CROM).

    Secondary Outcome Measures

    disability
    The neck disability index (NDI) will be used for measuring neck disability and it is a self-patient-completed questionnaire that measures patients' functional status. It contains 10 questions regarding pain, personal care, lifting, reading, headaches, concentration, work, driving, sleeping, and recreation. Each question has six answer choices scored from 0 to 5 as 0 indicates no disability and 5 indicates complete disability. All sections are scored then totaled on a scale from 0 to 50, as zero is the best possible score and 50 is the worst one
    pain intensity
    Visual Analogue Scale which is a 100-mm horizontal line will be used for measuring pain intensity. The patients will be instructed to represent their pain intensity level by marking anywhere on the line with "no pain" on the left side and "worst pain" on the right side
    rounded shoulder
    tape measurement will be used to to assess rounded shoulder: Subjects will be requested to stand normally with their hands hanging beside their bodies to test for rounded shoulder posture. Then, sternal notch, coracoid process, posteriolateral angle of the acromion process and the adjacent thoracic spinous process will be palpated and marked. The distance between sternal notch and coracoid process, and the distance between the posterolateral angle of the acromion process and the adjacent thoracic spinous process will measured by using tape
    pressure pain threshold
    pressure algometer device will be used for measuring pressure pain threshold

    Full Information

    First Posted
    February 8, 2023
    Last Updated
    February 8, 2023
    Sponsor
    Cairo University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05733429
    Brief Title
    Eye-Cervical Re-education Versus Motor Imagery Therapy on Proprioception in Chronic Mechanical Neck Pain
    Acronym
    MNP
    Official Title
    Eye-Cervical Re-education Versus Motor Imagery Therapy on Pain, Function, and Proprioception in Chronic Mechanical Neck Pain: A Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    March 2, 2023 (Anticipated)
    Primary Completion Date
    October 30, 2023 (Anticipated)
    Study Completion Date
    October 30, 2023 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Cairo University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    Brief Summary
    this study will be conducted to investigate the effect of eye-cervical re-education versus motor imagery therapy on pain intensity level, pain pressure threshold, neck disability, cervical proprioception, and scapular protraction in patients with chronic mechanical neck pain.
    Detailed Description
    Chronic neck pain is a common problem in modern and industrialized countries and among employed individuals. Pain is classified as chronic neck pain persists for more than 3 month, it may be felt all the time or worsen with certain activities. The cervical spine has an important role in providing the proprioceptive input and this is reflected in the abundance of cervical mechanoreceptors and their central and reflex connections to the vestibular, visual, and central nervous systems. Eye-cervical re-education program (ECRP) refer to a therapeutic procedure for correcting posture cephalic level in patients with cervical pain by improving eye-neck proprioception that reduced symptoms experienced by patients and improvement of the quality of cervical afferent input into the central nervous system. Motor imagery is the mental realization of motion without any motion occurs. It has two categories: kinesthetics and visual imagery. Kinaesthetic imagery is the situation of feeling a motion. Visual imagery has two types: internal visual and external visual. In the internal visual imagery, the motion is visualized within the body by seeing feet and arms. The external visual imagery is that one sees himself/herself from outside. one hundred and twenty patients will be allocated randomly into three groups; group A will receive eye cervical re-education and conventional therapy, group B will receive motor imagery therapy and conventional therapy and group C will receive conventional therapy only three times a week for four weeks.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Neck Pain
    Keywords
    Eye-Cervical Re-education, Motor Imagery Therapy, neck pain

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    eye cervical re-education and motor imagery therapy
    Masking
    InvestigatorOutcomes Assessor
    Masking Description
    opaque sealed envelope
    Allocation
    Randomized
    Enrollment
    120 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    eye cervical re-education
    Arm Type
    Experimental
    Arm Description
    patients will receive eye cervical re-education three times a week for four weeks
    Arm Title
    motor imagery therapy
    Arm Type
    Experimental
    Arm Description
    patients will receive motor imagery therapy three times a week for four weeks
    Arm Title
    conventional physical therapy
    Arm Type
    Active Comparator
    Arm Description
    patients will receive conventional physical therapy three times a week for four weeks
    Intervention Type
    Other
    Intervention Name(s)
    eye cervical re-education
    Intervention Description
    patients will receive eye-cervical re-education in the form of 10 exercises at three phases; the first phase will include stimulation of ocular mobility, the second phase will consist of Cervical mobility exercise with restricted eye movement and the third phase will include stimulation of eye and neck movement co-ordination
    Intervention Type
    Other
    Intervention Name(s)
    motor imagery therapy
    Intervention Description
    the patients will receive motor imagery therapy for four weeks; the first week will receive kinesthetic imagery, the second week will receive visual imagery, the third week will receive action observation exercises with motor imagery and the fourth week will receive motor control exercises in front of a mirror.
    Intervention Type
    Other
    Intervention Name(s)
    conventional physical therapy
    Intervention Description
    the patients will receive conventional physical therapy programs in the form of hot packs, therapeutic massage, cervical isometric strengthening exercises, and scapular stabilization exercises.
    Primary Outcome Measure Information:
    Title
    joint position error
    Description
    The Cervical Joint Position Error (JPE) Test is a measurement tool used to clinically assess an individual's cervicocephalic proprioception ability. Cervicocephalic proprioception describes one's sense of position of their head and neck in space. The Cervical JPE Test measures the ability of a blindfolded patient to accurately relocate their head position back to a predetermined neutral point after cervical joint movement. The test is most commonly performed with head movement in the transverse and sagittal planes by cervical range of motion device (CROM).
    Time Frame
    up to four weeks
    Secondary Outcome Measure Information:
    Title
    disability
    Description
    The neck disability index (NDI) will be used for measuring neck disability and it is a self-patient-completed questionnaire that measures patients' functional status. It contains 10 questions regarding pain, personal care, lifting, reading, headaches, concentration, work, driving, sleeping, and recreation. Each question has six answer choices scored from 0 to 5 as 0 indicates no disability and 5 indicates complete disability. All sections are scored then totaled on a scale from 0 to 50, as zero is the best possible score and 50 is the worst one
    Time Frame
    up to four weeks
    Title
    pain intensity
    Description
    Visual Analogue Scale which is a 100-mm horizontal line will be used for measuring pain intensity. The patients will be instructed to represent their pain intensity level by marking anywhere on the line with "no pain" on the left side and "worst pain" on the right side
    Time Frame
    up to four weeks
    Title
    rounded shoulder
    Description
    tape measurement will be used to to assess rounded shoulder: Subjects will be requested to stand normally with their hands hanging beside their bodies to test for rounded shoulder posture. Then, sternal notch, coracoid process, posteriolateral angle of the acromion process and the adjacent thoracic spinous process will be palpated and marked. The distance between sternal notch and coracoid process, and the distance between the posterolateral angle of the acromion process and the adjacent thoracic spinous process will measured by using tape
    Time Frame
    up to four weeks
    Title
    pressure pain threshold
    Description
    pressure algometer device will be used for measuring pressure pain threshold
    Time Frame
    up to four weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    70 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age will range from 18 to 70 years Patients of both sexes. Neck pain diagnosed by physician greater than 3 months in duration. Active or latent myofascial trigger points (MTrPs) in at least one of the following muscles: upper trapezius, levator scapulae, or splenius capitis. Both active and latent MTrPs were considered because latent MTrPs have been associated with the development of sensory motor dysfunction and may contribute to different chronic musculoskeletal pain disorders Exclusion Criteria: Dizziness syndrome. Post-traumatic as whiplash Neurological, infectious, or tumor cervical pain. Pregnant women. Patients having speech and understanding problems. Past history of neck surgery Dizziness syndrome. Post-traumatic as whiplash. Neurological, infectious, or tumor cervical pain. Pregnant women. Patients having speech and understanding problems. Past history of neck surgery .
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    al shaymaa sh abd el azeim, lecturer
    Phone
    01033771553
    Email
    alshaymaa.shaaban@pt.cu.edu.eg
    First Name & Middle Initial & Last Name or Official Title & Degree
    al shaymaa sh abd el azeim, lecturer
    Phone
    01033771553
    Email
    alshaymaa.ahaaban@pt.cu.edu.eg

    12. IPD Sharing Statement

    Learn more about this trial

    Eye-Cervical Re-education Versus Motor Imagery Therapy on Proprioception in Chronic Mechanical Neck Pain

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