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Effect of Cervical stabilization versus mulligan mobilization with movement on selected cervical sagittal parameters in cervical radiculopthy.

Effect of Cervical stabilization versus mulligan mobilization with movement on selected cervical sagittal parameters in cervical radiculopthy.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202502486808699
Enrollment
60
Registered
2025-02-25
Start date
2025-03-01
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Musculoskeletal Diseases Nervous System Diseases

Interventions

Group A Conventional Treatment
Group B Mulligan Mobilization with Movement
Group C Cervical stabilization exercises

Sponsors

Faculty of Physical Therapy at Cairo University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Their ages range from 30 to 45 years. Neck pain for more than two months radiating unilaterally down to one arm over the dermatomal distributions of C6 and/or C7 nerve roots with or without restricted cervical spine mobility. The Neck Disability Index more than 20%. Positive 3 out of 4 elements of the following: spurling test, distraction test and upper limb tension test and ipsilateral cervical rotation less than 60 degrees

Exclusion criteria

Exclusion criteria: Temporomandibular joint problems. Primary upper extremity problem of local origin. Neurological deficits, Cognitive problems, vertebral fractures and previous history of spine surgery. Neck pain with vertigo or with bilateral upper limbs referred pain. Clinical instability, recent trauma and vertebrobasilar insufficiency. Structural abnormalities of the spine, osteoporosis, and spasmodic torticollis. Inflammatory or other specific disorders of spina such as ankylosing spondylitis and rheumatoid arthritis. Subjects with known pregnancy or systemic disorders as diabetes mellitus. Subjects with neck pain receiving physical therapy treatment continued in the last three months.

Design outcomes

Primary

MeasureTime frame
X-ray machine and computerized software to obtain sagittal cervical parameters through lateral view standing x-ray for cervical spine;Neck disability index (NDI) to determine baseline measurements for subjects with neck symptoms and to quantify functional disabilities

Secondary

MeasureTime frame
Biofeedback pressure unit to measure muscle activation and endurance of deep neck flexors through cranio-cervical flexion test.;A visual analog scale (VAS) to determine the intensity of neck pain. ;Cervical range of motion device (CROM) to obtain ROM of cervical spine.

Countries

Egypt

Contacts

Public ContactEbtesam Mohamed Fahmy

Professor of Neurology Faculty of Medicine Cairo University

em_fahmy@kasralainy.edu.eg00201002007077

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026