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Clinical Trials/NCT07599631
NCT07599631Not yet recruitingNot Applicable

Integrated Neuromuscular Inhibition Technique Versus Instrument-Assisted Soft Tissue Mobilization On Neck Disability, Endurance, and Proprioception Of Nonspecific Chronic Neck Pain

Cairo University0 sites60 target enrollmentStarted: May 25, 2026Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
60

Study Overview

Brief Summary

this study will be conducted to compare INIT versus IASTM on neck disability, cervical muscle endurance and proprioception, cervical alignment, pain intensity, pressure pain threshold in patients with neck pain

Detailed Description

Neck pain arises from a variety of factors, which may include ergonomic considerations and individual characteristics such as age, behavioral attitudes, or psychosocial issues like anxiety and job satisfaction. Since most cases of neck pain do not have a specific identifiable cause and are often linked to posture or mechanical issues, they are typically classified as nonspecific chronic neck pain. The primary goals of treating neck pain and MTrPs are to resolve the spasm, ease the pain, and deactivate the TrPs. One of these methods is the integrated neuromuscular inhibition technique (INIT). Instrument-assisted soft tissue mobilization (IASTM) with the M2T blade (M2T-Blade: IASTM Technology, Hamilton, ON, Canada) is a multifunctional instrument. Instrument-assisted soft tissue mobilization is inexpensive and has a variety of planes that can be used in treatment. Many studies have demonstrated its effectiveness in alleviating patients' symptoms.According to the literature, IASTM and INIT were effective as well as nonexhaustive treatment methods for patients experiencing mechanical neck pain. But there was a lack of literature that compared IASTM and INIT on neck disability, endurance, and proprioception on patients with neck pain.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Masking Description

opaque sealed envelope

Eligibility Criteria

Ages
18 Years to 50 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • All participants ages will range from 18 to 50 years.
  • BMI ranged from 18.5 to
  • have TrPs in their UT muscle, pain at rest, a jump sign when pressure is applied, limited range of motion (ROM), and referred pain.
  • The participants will report pain in the posterior or posterior lateral aspect of the neck in the previous 3 months

Exclusion Criteria

  • Participants of cervical spine disorders (cervical disc disease, cervical spondylitis, cervical myelopathy.
  • Participants with musculoskeletal conditions.
  • Pregnant women.
  • Participants with congenital postural deformities.
  • Participants who had a definite visual disability.

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Nabil Mahmoud Ismail Abdel-Aal

principle investigator : nabil mahmoud ismail

Cairo University

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