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Not yet recruitingNCT06799130Updated Jan 29, 2025

Instrument-Assisted Soft Tissue Mobilization Versus Muscle Energy Technique on Chronic Non-specific Neck Pain

An interventional study of instrument-assisted soft tissue mobilization and Muscle energy technique in CHRONIC NON-SPECIFIC NECK PAIN, sponsored by Cairo University. Not yet recruiting at 1 site in Egypt. Open to participants aged 18 Years to 35 Years. Per ClinicalTrials.gov, last updated 2025-01-29.

Sponsored by Cairo University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Mar 2025, 1 year 6 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
All
01

Study summary

the aim of this study is to investigate if there is any difference between INSTRUMENT-ASSISTED SOFT TISSUE MOBILIZATION and Muscle Energy Technique over sternocleidomastoid on Neck pain, Range of motion and Functional disability in patients with Chronic Non-specific Neck Pain

Read the detailed description

Non-specific neck pain (NSNP) is the most common and the 4th leading cause of musculoskeletal disorder worldwide. It is estimated that about 70% of the population experiences neck pain throughout life, with an annual incidence of 15% to 50%0. It is seen more commonly in middle-aged females. It has been well established that NSNP is not only the risk factor for developing severe spinal pathologies and functional disability but that it is also associated with decreasing the quality of life and productivity of workers. Pain, which leads to functional limitations especially in the cervical region, is associated with a decrease in the activation of the deep cervical flexors such as the longus colli and longus capitis muscles, and an increase in the activation of the superficial cervical flexors, such as SCM and anterior scalene muscles.It is reported that in individuals with CNP, there is an increase in the activation of SCM and anterior scalene muscles, especially during isometric cervical flexion and dynamic upper limb movements. In their study, Falla et al. concluded that individuals with unilateral CNP had muscle fatigue in their ipsilateral SCM and anterior scalene muscles. Wang et al. reported postural imbalance in individuals with CNP due to an increased activation and tightening of the suboccipital, SCM, upper trapezius, pectoralis, and rotator cuff muscles. A study by Mostafa et al., (2021) stated that IASTM has a favorable effect than conventional treatment in reduction mechanical neck pain, improvement cervical range of motion \&activity of daily living.

A Systematic Review by Sbardella et al., (2021) stated that all the studies analyzed show an effective improvement in the outcomes of pain, disability and joint function, which leads us to say that Muscle Energy Technique (MET) is certainly an effective and safe technique in the treatment of cervical pain.

this trail has three groups; one will receive IASTM+ conventional, the second will receive Muscle energy technique+ conventional and the third one will receive conventional treatment for four weeks

02

Conditions studied

  • CHRONIC NON-SPECIFIC NECK PAIN

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Keywords

  • instrument-assisted soft tissue mobilization
  • muscle energy technique
03

In context

Neck Pain

1,232 studies on the registry are indexed under Neck Pain; 255 are open to participants now.

This study's planned enrollment of 60 is above the median of 52 across 1,004 interventional studies indexed under Neck Pain.

Browse Neck Pain studies →

Lead sponsor

Cairo University is the lead sponsor of 4,780 studies on the registry; 1,427 are open to participants now.

Of its 36 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. The subjects are of both genders, aged between 18-35 years old .
  2. Subjects with Neck pain continued for at least the last 12 weeks .
  3. body mass index (18.5-24.9).

Exclusion criteria

Exclusion Criteria:

  1. Any specific neck pathology as radiculopathy, rheumatoid arthritis, and systemic diseases
  2. Sensory problems at the mid or upper back .
  3. A tendency to hemorrhage or anticoagulation treatment. And nonsteroidal pain medication .
  4. Signs of severe pathology such as malignancy, fractures of the cervical spine, cervical radiculopathy or myelopathy, or vascular syndromes such as vertebrobasilar insufficiency .
  5. surgery of the cervical spine, whiplash trauma (in the past or recent, as cause of the complaint).
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    instrument-assisted soft tissue mobilization

    the patients will receive instrument-assisted soft tissue mobilization twice a week for four weeks over sternocleidomastoid muscle bilaterally utilizing an M2T blade. The subject lay comfortably in supine position on a treatment table. After using alcohol swabs to clean the patient's skin and the blade, a lubricant (Vaseline) will be applied, and a sweeping technique will be utilized to administer a thorough yet comfortable soft tissue mobilization on the sternocleidomastoid from origin to insertion for roughly 3 minutes. conventional therapy the patients will receive hot back for 15 minutes, neck range of motion (ROM), chin tuck, stretches and strengthen exercise.

    Other: instrument-assisted soft tissue mobilization · Other: Muscle energy technique

  • Experimental
    Muscle energy technique

    the patients will receive post-isometric muscle relaxation(PIR) treatment for the sternocleidomastoid muscle, it will be applied from supine lying position with the head free from the plinth and held by the therapist's hand, the therapist placed one hand opposite the side of involvement muscle , The other hand is placed on the involved side of muscle . The patient pushed upward against the therapist's thumb on the forehead and looked up, then the patient will be asked to stop pushing and look down. After relaxation therapist will stretch the muscle for 30 seconds. This will be repeated 3 times bilaterally for 3 sessions per week for four weeks. conventional therapy the patients will receive hot back for 15 minutes, neck range of motion, chin tuck, stretches and strengthen exercise.

    Other: instrument-assisted soft tissue mobilization · Other: Muscle energy technique

  • Active comparator
    conventional therapy

    the patients will receive conventional therapy three times a week for four weeks conventional therapy the patients will receive hot back for 15 minutes, neck range of motion (ROM), chin tuck, stretches and strengthen exercise.

    Other: instrument-assisted soft tissue mobilization · Other: Muscle energy technique

Interventions

  • Otherinstrument-assisted soft tissue mobilization

    instrument-assisted soft tissue mobilization

    Also known as: IASTM

  • OtherMuscle energy technique

    Muscle energy technique

06

What researchers measure

Primary outcomes

  1. pain intensity

    the scale that will be used is VAS ; each subject will be instructed to put point on line from no pain to tolerable pain

    Time frame: up to four weeks

Secondary outcomes

  1. neck range of motion

    will be measured by cervical range of motion device (CROM)

    Time frame: up to four weeks

  2. neck disability

    will be measured by Arabic version of neck disability index

    Time frame: up to four weeks

07

Study locations

1 site
  • Alaa Mohamed Hassan Saleh
    Cairo, 00, Egypt
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 29, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06799130
Lead sponsor
Cairo University
Responsible party
alaa mohamed hassan saleh (Principal Investigator, Cairo University) — Principal investigator
First posted
Jan 29, 2025
Start date
Jan 29, 2025 (estimated)
Primary completion
Mar 15, 2025 (estimated)
Completion
Mar 30, 2025 (estimated)
Last update
Jan 29, 2025

Study contacts

alaa saleh
Contact
alaanaqib168@gmail.com
01121746761
alaa saleh
principal investigator · Cairo University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jan 2025. You cannot join it, but the record below documents what was studied.

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