- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06603779
Integrated Neuromuscular Inhibition Versus Cervical and Scapular Stabilization Exercises on Myofascial Trigger Points of Upper Trapezius
August 24, 2025 updated by: Dina Al-Amir Mohamed Hussein, Beni-Suef University
Integrated Neuromuscular Inhibition Versus Cervical and Scapular Stabilization Exercises on Myofascial Trigger Points of Upper Trapezius: Randomized Controlled Trial.
This trial will involve three groups.
The Integrated Neuromuscular Inhibition group will receive the integrated neuromuscular inhibition technique.
The cervical and Scapular stabilization group will receive cervical and scapular stabilization exercises.
The ultrasound group will receive ultrasound therapy
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
46
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
-
-
-
Banī Suwayf, Egypt
- Faculty of Physical Therapy
-
-
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:
- Patients with active trigger points in the upper trapezius for more than 2 weeks based on the Simons Criteria.
- Age ranged from 18-25 years.
- Pain intensity ≥ 3 on VAS.
- Females and males.
Exclusion Criteria:
- Patients indicated for surgery.
- Patients with symptomatic disc lesions.
- Patients with rheumatological diseases or traumatic neck injury.
- Patients injected with corticosteroids in the last 6 months.
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 Group
This group will receive the Integrated Neuromuscular Inhibition Technique which consists of ischemic compression, strain counter strain, and muscle energy technique
|
Integrated Neuromuscular technique is a kind of Manual therapy which include Ischemic Compression, Strain counter-strain and muscle energy technique
|
|
Experimental: Cervical and Scapular Stabilization exercises Group
This group will receive a group of exercises for the neck and scapula which will strengthen both of them
|
Cervical and Scapular Stabilization exercises are a group of therapeutic exercises.
|
|
Placebo Comparator: Ultrasound Therapy Group
This group will receive ultrasound Therapy
|
a device that transmit ultrasound waves to the participant through direct contact
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual Analogue Scale (VAS)
Time Frame: 1-3 months
|
Visual Analogue Scale is a scale that measures pain intensity.
Subjects will instructed to indicate their current pain by marking a point on a 10 mm transverse line with 0 degrees meaning "no pain" and 10 meaning the "worst pain"
|
1-3 months
|
|
Pressure Pain Algometer
Time Frame: 1-3 months
|
The pressure pain Algometer is a device that measures the pain threshold of the subjects.
|
1-3 months
|
|
Neck Pain and Disability Questionnaire (NDI)
Time Frame: 1-3 months
|
Neck Pain and Disability is a questionnaire that measures neck pain and disabilities in subjects.
Each question in the questionnaire will explained in detail and the subject will be asked to select one sentence out of six that best describes their function, a higher score indicates a great loss of function.
|
1-3 months
|
|
36-item Short-Form Health Questionnaire
Time Frame: 1-3 months
|
36-item Short-Form Health Questionnaire will measure quality of life
|
1-3 months
|
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)
October 1, 2024
Primary Completion (Actual)
July 28, 2025
Study Completion (Actual)
July 28, 2025
Study Registration Dates
First Submitted
September 12, 2024
First Submitted That Met QC Criteria
September 17, 2024
First Posted (Actual)
September 19, 2024
Study Record Updates
Last Update Posted (Estimated)
August 26, 2025
Last Update Submitted That Met QC Criteria
August 24, 2025
Last Verified
August 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Beni-Suef University22
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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