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Adding Low Frequancy High Intensty Magnetic Therapy to Cervical Stabilization Exercises in Cervical Spondylosis

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What is being tested

low Frequency High Intensity magnetic therapy

Device
Who is being recruted

Bone Diseases+1

+ Musculoskeletal Diseases

+ Spinal Diseases

From 30 to 45 Years
See all eligibility criteria
How is the trial designed

Treatment Study

Placebo-Controlled
Interventional
Study Start: February 2023
See protocol details

Summary

Principal SponsorDelta University for Science and Technology
Study ContactAl zahraa F Morshed, MSC
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: February 1, 2023

Actual date on which the first participant was enrolled.

Cervical spondylosis is a chronic degenerative process of the cervical spine. Pain in the neck and/or arms, neck stiffness, and headaches are the usual symptoms of cervical spondylosis . Low frequency high intensity magnetic therapy causes short term immediate effect in the relieve pain and improve function in patients with cervical spondylosis . Cervical stabilization causes decrease in neck pain and neck disability as well as a significant increase in cervical muscle endurance and cervical range of motion after the intervention. It also demonstrates a more ideal upper body posture and improved cervical proprioception. In the present study, therefore, we aimed to investigate adding low frequency high intensity magnetic therapy to CSE on management of cervical spondylosis. This study will be a benefit in the physical therapy field and may guide rehabilitation programs of physical therapy towards better results through decreasing time needed to perform activity of daily living, decreasing dependency and making patient an active member in society.

Official TitleAdding Low Frequancy High Intensty Magnetic Therapy to Cervical Stabilization Exercises in Cervical Spondylosis
NCT05734924
Principal SponsorDelta University for Science and Technology
Study ContactAl zahraa F Morshed, MSC
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

80 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 30 to 45 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Bone DiseasesMusculoskeletal DiseasesSpinal DiseasesSpondylosis

Criteria

Inclusion Criteria: * Eighty Cervical spondylosis patients from both sexes will be participated in this study. * The patients' ages will be ranged from 30-45 years to prevent aging process. * X-ray evidence of cervical spondylosis (osteophyte formation, intervertebral disc height narrowing and vertebral end-plate sclerosis) . * The presence of chronic neck pain (more than 3 months). * Limited mobility in the cervical spine. Exclusion Criteria: * The following patients will be excluded from the study patients with: * History of cervical injury of trauma. * Cervical myelopathy. * Inflammatory arthritis involving cervical spine. * Tumor or infection involving cervical spine. * Vertebrobasilar artery insufficiency. * Neurologic disease (e.g. multiple sclerosis, Parkinson's disease, syringomyelia). * Congenital anomalies involving cervical spine. * Diabetes mellitus. * Vestibular system impairments.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

50% chance of being blinded to the placebo group

Treatment Groups

Group I

Sham
The patient in this group will sham magnetic therapy in addition to, cervical stabilization exercise protocol; treatment will conduct for 3 times/ week for five weeks.

Group II

Active Comparator
The patient in this group will received low Frequency High Intensity magnetic therapy with frequency 50 Hz and high intensity 60mT for 30 minutes /session, treatment will be conducted for 3times/week for five weeks combined with cervical stabilization exercise protocol

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

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