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RecruitingNCT06468904Updated Jun 26, 2024

Efficacy of Cervical Stabilization Exercises on Hand Grip Strength in Chronic Myofascial Neck Pain

An interventional study of cervical stabilization exercises and integrated neuromuscular technique. in Chronic Neck Pain, sponsored by Cairo University. Recruiting at 2 sites in Egypt. Open to female participants aged 20 Years to 45 Years. Per ClinicalTrials.gov, last updated 2024-06-26.

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

From the registry’s dates

  • Primary completion was expected by Aug 2024, 2 years 2 months ago, but the record still lists the study as recruiting.
  • Registered 8 months after the study started (first participant enrolled Oct 2023, registered Jun 2024).
  • Started Oct 2023; still recruiting 3 years later.
Phase
Not applicable
Study type
Interventional
Enrollment
52
Allocation
Randomized
Ages
20 Years to 45 Years
Sex
Female
01

Study summary

The purpose of this study is to examine effect of cervical stabilization exercises on hand grip strength, key pinch strength, pain intensity, pain pressure threshold and hand function in chronic myofascial neck pain patients.

Read the detailed description

Myofascial pain of the trapezius is considered one of the main causes of neck pain and characterized by deep, intense pain of the skeletal muscles and their fascia and by the presence of one or more MTrPs, Although MTrPs can be formed in any muscle or muscle group, previous studies concluded that the upper trapezius(UT) muscle is the most commonly affected muscle.

Considering the role of synergistic function of the UT muscle in scapula-humeral rhythm during shoulder movement, it is not surprising that MTrPs in UT muscle can result in shoulder dysfunction and disability. Muscle activity of proximal parts is necessary for activation of distal parts. In fact, the stable activity of distal parts needs controlling the proximal parts. Thus, the stability of shoulder girdle is required for activity of distal parts such as fingers, wrists and elbows. In addition, trigger points in the UT can affect grip strength, which depends on shoulder joint and scapular stability. Thus, UT muscle dysfunction can reduce grip strength.

However, little research has been carried out to determine the therapeutic effects of cervical stabilization exercises on chronic neck pain, and up till now, there is a gap in literature to explore efficacy of cervical stabilization exercises on chronic neck pain and hand grip strength. Therefore, this study aims to investigate whether cervical stabilization exercises has an effect on hand grip strength in chronic myofascial neck pain.

02

Conditions studied

  • Chronic Neck Pain

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Keywords

  • cervical stabilization
  • hand grip
  • myofascial neck pain
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 52 is close to 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
20 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  1. Chronic neck pain for more than 3 months.
  2. Active MTrPs in the UT muscle with a tender nodule.
  3. Constant neck pain, a jump sign during palpation of UT muscle.
  4. Referred pain.
  5. Symptoms of ipsilateral hand muscles weakness.

Exclusion criteria

Exclusion Criteria:

  1. Signs of severe pathology such as malignancy of the cervical area.
  2. Fractures of the cervical spine.
  3. Cervical radiculopathy or myelopathy.
  4. Diabetes.
  5. Trauma, congenital anomalies and surgery around neck, shoulder and hand.
  6. Fibromyalgia or vascular syndromes such as vertebra-basilar insufficiency.
  7. Pregnancy.
05

Study design

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

Study arms

  • Experimental
    cervical stabilization exercises and integrated neuromuscular inhibition technique

    patients received cervical stabilization exercises and integrated neuromuscular inhibition technique for 3 sessions / week for 4 weeks. Cervical stabilization included chin tucks, isometric holds, ball squeeze. Integrated neuromuscular inhibition technique included: 1. ischemic compression: therapist applied an intermittent ischemic compression on upper trapezius trigger point by thumb for 90sec. 2. Strain counter-strain: therapist applied pressure at trigger point. patient's head was laterally flexed towards the affected side passively by one hand of the therapist. The other hand held the subject's forearm and moved the affected shoulder to 90degree of abduction and external rotation for 90 secs. 3. Muscle energy technique: patient laterally flexed the neck to opposite side patient was moved the stabilized shoulder and ear towards each other. The contraction was maintained for 10 sec followed by 5 seconds of relaxation. The muscle was stretched for 30 secs.

    Procedure: cervical stabilization exercises and integrated neuromuscular technique.

  • Active comparator
    Integrated neuromuscular inhibition technique

    patients received integrated neuromuscular inhibition technique for 3 sessions / week for 4 weeks.it included Ischemic compression, Strain counter-strain and muscle energy technique. 1. ischemic compression. therapist applied an intermittent ischemic compression on upper trapezius trigger point by thumb for 90 sec. 2. Strain counter-strain: therapist applied pressure at trigger point. patient laterally flexed towards the affected side passively by one hand of the therapist. The other hand held the subject's forearm and moved the affected side shoulder passively to 90degree of abduction and external rotation for 90 secs. 3. Muscle energy technique: patient was asked to laterally flex the neck to opposite side. patient was requested to move the stabilized shoulder and ear towards each other. The contraction was maintained for 10 sec followed by 5 seconds of relaxation. The muscle was stretched for 30 secs.

    Procedure: cervical stabilization exercises and integrated neuromuscular technique.

Interventions

  • Procedurecervical stabilization exercises and integrated neuromuscular technique.

    Patients received cervical stabilization exercises and integrated neuromuscular inhibition technique. Cervical stabilization protocol included strengthening exercises of deep cervical flexors muscles which included chin tucks, isometric holds, ball squeeze, as well as deep cervical extensors muscles which included cranio-cervical flexion from neutral, upper cervical rotation and extension of cervical spine. integrated technique includes ischemic compression, muscle energy technique and strain counter strain.

06

What researchers measure

Primary outcomes

  1. primary outcome measure

    hand grip strength was measured by hand held dynamometer.

    Time frame: up to four weeks

Secondary outcomes

  1. secondary outcome measures

    pain pressure threshold was measured by pressure algometer.

    Time frame: up to four weeks

  2. secondary outcome measure

    hand function was measured by michigan quesstionaire.The Michigan Hand Outcomes Measure comprises 37 items with rating scale ranging 1 to 5. Every single domain was scored and converted to values that range from 0-100. A high score indicates better results, with the exception of pain in which a high score indicates a more intense pain.

    Time frame: up to four weeks

  3. secondary outcome measure

    pain intensity was measured by visual analogue scale.The level of pain on the VAS was recorded on a 10 cm line distinct at one end 'no pain' and marked at the other end 'the worst pain. Subjects were asked to state their pain level by placing a mark on this horizontal line

    Time frame: up to 4 weeks

  4. secondary outcome measure

    pinch strength was measured by pinch gauge

    Time frame: up to four weeks

07

Study locations

1 of 2 sites recruiting
  • Cairo University
    Giza, 11251, Egypt
    Completed
  • Faculty of physical therapy
    Giza, 11251, Egypt
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 26, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06468904
Lead sponsor
Cairo University
Responsible party
Fatma Alzahraa Mohamed Ali Ramadan (principle invesyigator, Cairo University) — Principal investigator
First posted
Jun 21, 2024
Start date
Oct 1, 2023
Primary completion
Aug 2024 (estimated)
Completion
Aug 2024 (estimated)
Last update
Jun 26, 2024

Study contacts

Fatma Alzahraa M Ali, Master
Contact
fatmaalzahraa@pt.bsu.edu.eg
01028371924
soheir sh Rezkallah, PHD
study director · professor of physaical therapy
Ghada Abd Elmoneim, PHD
study director · assistant professor of physical therapy
Haidy S Roshdy, PHD
study director · lecturer of physical therapy

Oversight

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

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