- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05439018
Effect of Integrated Neuromuscular Inhibition Technique on Subjects with Neck Pain and Forward Head Posture
March 14, 2025 updated by: Somaya Nady Mohamed Elsayed, Cairo University
- To investigate the effects of integrated neuromuscular inhibition technique for upper trapezius and suboccipital muscles on craniovertebral angle in neck pain and forward head posture subjects.
- To investigate the effects of integrated neuromuscular inhibition technique for upper trapezius and suboccipital muscles cervical pain intensity level in neck pain and forward head posture subjects.
- To investigate the effects of integrated neuromuscular inhibition technique for upper trapezius and suboccipital muscles on cervical range of motion in neck pain and forward head posture subjects.
- To investigate the effects of integrated neuromuscular inhibition technique for upper trapezius and suboccipital muscles on cervical proprioception in neck pain and forward head posture subjects.
- To investigate the effects of integrated neuromuscular inhibition technique for upper trapezius and suboccipital muscles cervical function in neck pain and forward head posture subjects.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Forward head posture (FHP) is one of the most common types of postural abnormality, and it is generally described as an anterior position of the head in relation to the vertical line of the body's center of gravity.
Many researchers have reported that several factors, including headache, neck pain, and musculoskeletal disorders such as temporomandibular disorders or rounded shoulders, are related to FHP .
It is associated with shortening of the upper trapezius, the posterior cervical extensor muscles, the sternocleidomastoid muscle and the levator scapulae muscle Forward head posture (FHP) is a forward inclination of the head with cervical spine hyperextension and is associated with shortening of the upper trapezius, the splenius and semispinalis capitis and crevice's, the cervical erector spinae and the levator scapulae musculature .
A significant number of the population experiences neck related musculoskeletal problems caused by abnormal forward head posture.
Forward Head Posture (FHP) is a common postural deviation reported in the literature, and has been considered as a risk factor for the development of neck pain.
Around 61.3% adults with neck pain, working using computers were reported to have FHP In addition, patients with chronic neck pain demonstrated weakness in their deep neck flexors and presented with FHP when distracted.
Neck pain is a common disorder characterized by pain, discomfort or soreness experienced in a region between the inferior margin of the occipital bone and T1.
Prevalence of neck pain in employees is not the same all over the world.
In western countries it has been reported to be between 34% and 54%.As neck pain could become a chronic and disabling symptom, discovering and controlling risk factors seems to be a reasonable prevention strategy.
Improper posture could be improved by education and proper reminders to decrease the prevalence of neck pain and increase the quality of life.
It is thought that adolescents or patients with neck pain (NP) have a more forward head posture, thus a smaller craniovertebral (CV) angle than age-matched pain-free participants.
It was concluded that the CV angle is negatively correlated with the disability of patients with neck pain.
So, patients with small CV angle have a greater forward head posture, and the greater the forward head posture, the greater the disability
Study Type
Interventional
Enrollment (Actual)
40
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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Cairo, Egypt
- Faculty of Physical Therapy
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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
14 years to 19 years (Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- - Adolescent Female physical therapy students between 18-23 years old
- BMI between 18.5-25 kg/m²
- Symptomatic forward head posture with CVA 49° or less.
- Latent trigger point
- Neck pain more than 3 months
Exclusion Criteria:
- Cervical disc
- Myelopathy or cervical radiculopathy
- Cervical spine surgery in the past
- Having received physical therapy in the three months prior to the study
- Non- rheumatologic diseases as multiple sclerosis, thyroid dysfunction and chronic infection.
- Rheumatologic condition as poly-articular osteoarthritis, rheumatoid arthritis and advanced cervical spine degenerative diseases. -
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: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Integrated Neuromuscular Inhibition
Integrated Neuromuscular Inhibition in addition to traditional treatment will be received three times a week for eight weeks.
Integrated Neuromuscular Inhibition will be contain three combined manual treatment ( ischemic compression , strain counter strain , Muscle energy technique )
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Integrated Neuromuscular Inhibition in addition to traditional treatment will be received three times a week for eight weeks.
Integrated Neuromuscular Inhibition will be contain three combined manual treatment ( ischemic compression , strain counter strain , Muscle energy technique ) traditional treatment will be received three times a week for eight weeks .
traditional treatment in Form of stretching and strenghthening of cervical muscles and postural advices
Other Names:
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|
Active Comparator: traditional treatment
traditional treatment will be received three times a week for eight weeks .
traditional treatment in Form of stretching and strenghthening of cervical muscles and postural advices
|
traditional treatment will be received three times a week for eight weeks .
traditional treatment in Form of stretching and strenghthening of cervical muscles and postural advices
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Craniovertebral angle
Time Frame: up to eight weeks
|
Craniovertebral angle (CVA): is the angle formed between a horizontal line through the spinous process of C7 and a line from the tragus of the ear
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up to eight weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Neck pain intensity level
Time Frame: up to eight weeks
|
Neck pain will measured by visual analogue scale ( VAS) .When responding to a VAS item, patients make marks along 100 mm line at the point they feel represents their current pain state . with 100 mm means high level of pain and 0 means no pain |
up to eight weeks
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change in Neck Functional disability
Time Frame: up to eight weeks
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Neck disability will measured by English neck disability index (NDI) Questionnaire is composed of a total of 10 questions.Each question has 6 answer options which pertain to a level of severity (0-5) with total score of 50 ,when NDI is high the neck function is the worst
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up to eight weeks
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Cervical Range of motion ROM
Time Frame: up to eight weeks
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Cervical Range of motion will measured by clinometer application
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up to eight weeks
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Cervical proprioception
Time Frame: up to eight weeks
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Cervical proprioception will measured by clinometer application
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up to eight weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Saadat Z, Hemmati L, Pirouzi S, Ataollahi M, Ali-Mohammadi F. Effects of Integrated Neuromuscular Inhibition Technique on pain threshold and pain intensity in patients with upper trapezius trigger points. J Bodyw Mov Ther. 2018 Oct;22(4):937-940. doi: 10.1016/j.jbmt.2018.01.002. Epub 2018 Jan 17.
- Mohamed DA, Kamal RM, Gaber MM, Aneis YM. Combined Effects of Extracorporeal Shockwave Therapy and Integrated Neuromuscular Inhibition on Myofascial Trigger Points of Upper Trapezius: A Randomized Controlled Trial. Ann Rehabil Med. 2021 Aug;45(4):284-293. doi: 10.5535/arm.21018. Epub 2021 Aug 30.
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)
October 1, 2022
Primary Completion (Actual)
December 30, 2022
Study Completion (Actual)
January 1, 2023
Study Registration Dates
First Submitted
June 23, 2022
First Submitted That Met QC Criteria
June 29, 2022
First Posted (Actual)
June 30, 2022
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
March 14, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- INMI on neck pain and FHP
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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