- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06695299
Kinesthetic and Visual Motor Imagery on Cervical Position Sense and Balance in Mechanical Neck Pain
January 30, 2025 updated by: Lama Saad El-Din Mahmoud, October 6 University
Effect of Kinesthetic and Visual Motor Imagery Training on Cervical Position Sense and Balance in Patients With Mechanical Neck Pain
To investigate the Effect of Kinesthetic and Visual Motor Imagery Training on Cervical Position Sense and Balance in Mechanical Neck Pain
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Thirty patients with Mechanical Neck Pain will participate in this study.
The patients will randomly be divided into two equal groups; the control group which received the selected exercise program and the study group received the same exercise training program in addition to Kinesthetic and Visual Motor Imagery Training, three times per week for four weeks.
The evaluation methods are cervical joint position error test, neck disability index, multidirectional reach test and visual analogue scale
Study Type
Interventional
Enrollment (Actual)
44
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Select State
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Al Jīzah, Select State, Egypt, 0020
- Lama Saad El-Din Mahmoud
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- thirty patients with mechanical neck pain,
- Age will range as (35:50) years old
- body mass index (18:29)
Exclusion Criteria:
- difficulty to communicate or to understand program instructions
- any other neurological deficits or orthopaedic abnormalities,
- secondary musculoskeletal complication
- Cervical disc prolapses
- Any other cervical problem
- Spinal stenosis
- Previous spinal surgery
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: control group
the control group which received the selected exercise program
|
therapeutic ultrasound, Static neck exercise, balance exercises
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|
Experimental: study group
the study group received the selected exercise program in addition to Kinesthetic and Visual Motor Imagery Training
|
therapeutic ultrasound, Static neck exercise, balance exercises
Kinesthetic and Visual Motor Imagery Training During kinesthetic imagery, the participants were asked to feel their body parts without any body motion.
During visual imagery, the participants were asked to perform a visual presentation of the motion without any body motion.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
cervical joint position error test
Time Frame: four weeks
|
The subject will be instructed to perform an active head rotation to one side, after which returns back to the neutral or starting head position. The test will be performed in a 3 trials in each direction |
four weeks
|
|
Neck disability index
Time Frame: four weeks
|
includes 10 items as follows: Pain Intensity, Personal Care, Lifting, Reading, Headaches, Concentration, Work, Driving, Sleeping, and Recreation, with a score (0:5) for every point.
The maximum score is 50, with the interpretation scoring (no disability = 0: 4, mild disability 5:14, moderate disability 15:24, severe disability 25: 34 and complete disability above 34
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four weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual analogue scale for pain (VAS-P)
Time Frame: four weeks
|
is a method for measuring the intensity of pain on a horizontal straight line of fixed length (10 cm), as the left end of the line showed the greatest pain score & the right end showed the least pain scores, then the patient was asked to put a mark, on the line according to his/her pain sensation, with a higher score representing the higher level of pain
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four weeks
|
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multidirectional reach test
Time Frame: four weeks
|
The Multi-Directional Reach Test (MDRT) measures balance and the limits of stability in the anterior-posterior and medial-lateral directions by testing how far an individual can voluntarily reach forward, to the right, to the left, and lean backward, while standing with their feet flat on the ground, shoulder-width apart
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four weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 15, 2024
Primary Completion (Actual)
November 30, 2024
Study Completion (Actual)
December 15, 2024
Study Registration Dates
First Submitted
November 16, 2024
First Submitted That Met QC Criteria
November 16, 2024
First Posted (Actual)
November 19, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 30, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/005399
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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