NCT05733429

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.

Trial Health

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2023

Shorter than P25 for not_applicable

Status
unknown

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

February 8, 2023

Completed
9 days until next milestone

First Posted

Study publicly available on registry

February 17, 2023

Completed
13 days until next milestone

Study Start

First participant enrolled

March 2, 2023

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 30, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 30, 2023

Completed
Last Updated

February 17, 2023

Status Verified

February 1, 2023

Enrollment Period

8 months

First QC Date

February 8, 2023

Last Update Submit

February 8, 2023

Conditions

Keywords

Eye-Cervical Re-educationMotor Imagery Therapyneck pain

Outcome Measures

Primary Outcomes (1)

  • 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).

    up to four weeks

Secondary Outcomes (4)

  • disability

    up to four weeks

  • pain intensity

    up to four weeks

  • rounded shoulder

    up to four weeks

  • pressure pain threshold

    up to four weeks

Study Arms (3)

eye cervical re-education

EXPERIMENTAL

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

Other: eye cervical re-educationOther: conventional physical therapy

motor imagery therapy

EXPERIMENTAL

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

Other: motor imagery therapyOther: conventional physical therapy

conventional physical therapy

ACTIVE COMPARATOR

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

Other: conventional physical therapy

Interventions

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

eye cervical re-education

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.

motor imagery therapy

the patients will receive conventional physical therapy programs in the form of hot packs, therapeutic massage, cervical isometric strengthening exercises, and scapular stabilization exercises.

conventional physical therapyeye cervical re-educationmotor imagery therapy

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • 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 .

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Neck Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

al shaymaa sh abd el azeim, lecturer

CONTACT

al shaymaa sh abd el azeim, lecturer

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Masking Details
opaque sealed envelope
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: eye cervical re-education and motor imagery therapy
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Nabil mahmoud ismail

Study Record Dates

First Submitted

February 8, 2023

First Posted

February 17, 2023

Study Start

March 2, 2023

Primary Completion

October 30, 2023

Study Completion

October 30, 2023

Last Updated

February 17, 2023

Record last verified: 2023-02