Influence of Cervical Stabilization Exercises on Neural Tissue Mechanosensitivity in Patients With Chronic Nonspecific Neck Pain
NP
1 other identifier
interventional
80
0 countries
N/A
Brief Summary
this study will be conducted to investigate the effect of cervical stabilization exercises on cervical pain intensity, upper limbs mechanosensitivity, cervicovertebral angle, and cervical proprioception in individuals with chronic nonspecific neck pain
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jan 2026
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 5, 2026
CompletedFirst Posted
Study publicly available on registry
January 14, 2026
CompletedStudy Start
First participant enrolled
January 15, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 15, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 25, 2026
January 14, 2026
January 1, 2026
5 months
January 5, 2026
January 5, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
mechanosensitivity of upper limb nerves
A handheld algometer will be used to assess mechanosensitivity. To apply this test test, specific points on the peripheral nerve trunks of the tested upper limb nerves will be identified through manual palpation, being easily accessible by the probe of the algometer and as they are commonly used sites of peripheral nerves' palpation with moderate inter-tester reliability. The supine lying posture will be assumed to test median and ulnar nerves, while sitting posture will be the choice for radial nerve. Median nerve will be located and tested in the antebrachial fossa just medial to the biceps brachii tendon. Ulnar will be tested in the cubital tunnel between humeral medial epicondyle and olecranon process, with the arm in 90º shoulder abduction as well as external rotation, and elbow flexion. Radial nerve palpation point lies between the middle and lower thirds of the humerus.
up to 6 weeks
Secondary Outcomes (3)
craniovertebral angle
up to 6 weeks
pain intensity
up to six weeks
cervical joint position error (cervical proprioception)
up to six weeks
Study Arms (2)
cervical and scapulothoracic stabilization exercises.
EXPERIMENTALforty patients will receive cervical and scapulothoracic stabilization exercises plus traditional therapy three times a week for six weeks
traditional therapy
ACTIVE COMPARATORforty patients will receive traditional therapy three times a week for six weeks
Interventions
the patients will receive traditional therapy in the form of ultrasound, hot pack, cervical extensors stretching and deep flexor strengthening
the patients will receive cervical and scapulothoracic stabilization exercises in the form of activation of deep cervical flexors in the first two weeks, followed by scapulothoracic muscles activation for the third and fourth weeks and finally group of exercises that emphasis on increasing difficulty and progress to quadruped and standing.
Eligibility Criteria
You may qualify if:
- participants with age range from 18 to 36 years and BMI from 25 to 30kg/m2 will be recruited
- Participants having neck pain symptoms provoked by neck postures, neck movement, or palpation of the cervical musculature, for 3 months
- Patients with a craniovertebral angle of less than 50º
You may not qualify if:
- History of previous injury of the neck.
- History of surgical intervention at the neck.
- History of inflammatory joint disease affecting facet joints
- participants with congenital disorders of the cervical spine.
- participants who received pain medication or physical therapy for their neck pain during the last 3 months.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- opaque sealed envelope
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- principle investigator : nada ashraf mohamed zuhairy
Study Record Dates
First Submitted
January 5, 2026
First Posted
January 14, 2026
Study Start
January 15, 2026
Primary Completion (Estimated)
June 15, 2026
Study Completion (Estimated)
June 25, 2026
Last Updated
January 14, 2026
Record last verified: 2026-01