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Proprioceptive Paradigm in addition to strength training program in cervical radiculopathy.

EFFECTIVENESS OF PROPRIOCEPTIVE PARADIGM IN ADDITION TO STRENGTH TRAINING PROGRAM IN CERVICAL RADICULOPATHY

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240513061777N1
Enrollment
56
Registered
2024-08-02
Start date
2024-01-01
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Cervical Radiculopathy. Cervical disc disorder with radiculopathy

Interventions

Intervention 1: Intervention group: Proprioceptive Training Paradigm, Hot pack, TENS, Myofascial Release, Strength Training. Intervention 2: Control group: Hot pack, TENS, Myofascial Release, Strength

Sponsors

The University of Lahore
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 55 Years

Inclusion criteria

Inclusion criteria: Age between 30-55 years. Both male and female. Patients with pain or numbness of one or both arms. Duration of symptoms is from more than 3 months. Patients from both genders are diagnosed according to a careful clinical evaluation by the neurologist and diagnosis were confirmed radiologically by MRI and X-ray findings of the cervical spine. To confirm the diagnosis of CR in addition to X-ray and MRI, Spurling test, upper limb tension test can also be used (Wang, 2022) All patients are medically and psychologically stable (Kamal et al.).

Exclusion criteria

Exclusion criteria: Past fracture or surgery in cervical spine. Deformity of the spine. Inflammatory rheumatologic disease. Vertebro basilar artery insufficiency. Malignancy. Cervical myelopathy. Cervical myelo-radiculopathy.

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Pre-treatment and Post-treatment. Method of measurement: Visual Analog Scale.

Secondary

MeasureTime frame
Functional Disability. Timepoint: pre-treatment and Post-treatment. Method of measurement: NDI.;ROM. Timepoint: Pre-treatment and Post-treatment. Method of measurement: Laser Pointer Device.

Countries

Pakistan

Contacts

Public ContactUfaq Hafeez

The University of Lahore

ufaqansari2014@gmail.com+92 333 6125893

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026