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Comparison of routine and specific therapeutic exercise after cervical spine disc herniation surgery

Comparison of specific and routine therapeutic exercises after cervical spine disc herniation surgery on functional disability, pain and neck muscle morphology

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221019056245N2
Enrollment
60
Registered
2023-08-20
Start date
2023-09-01
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Neck surgery due to cervical disc herniation. Other cervical disc degeneration

Interventions

Intervention 1: Intervention group: The intervention group will perform routine care in addition to specific exercises for eight weeks, three times a week for forty minutes each time. Intervention 2:

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
46 Years to 70 Years

Inclusion criteria

Inclusion criteria: Aged 46 - 70 years old Continuous and treatment-resistant pain caused by cervical spine disc herniation for at least 2 months Clinical findings confirmed by MRI Weakness of upper limb or limbs before surgery Patients who underwent surgery with an anterior approach

Exclusion criteria

Exclusion criteria: History of previous surgery Pain greater than score 8 after surgery based on VAS Need for re-surgery Surgery caused by systemic diseases Surgery due to fracture Surgery caused by infection Decreased range of motion due to osteophyte and fusion of vertebrae

Design outcomes

Primary

MeasureTime frame
Functional ability. Timepoint: Before the intervention and after the intervention. Method of measurement: Neck Pain Disability Questionnaire.;Morphology of the deep cervical muscles. Timepoint: Before the intervention and after the intervention. Method of measurement: By the ultrasonography device.

Secondary

MeasureTime frame
Pain intensity. Timepoint: Before the intervention and after the intervention. Method of measurement: Pain intensity Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKhodabakhsh Javanshir

Babol University of Medical Sciences

khodabakhshjavanshir@gmail.com+98 11 3219 9592

Outcome results

None listed

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