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Effects of Complex Rehabilitation Program on Reducing Pain and Disability in Patients with Lumbar Disc Protrusion.

Effects of Complex Rehabilitation Program on Reducing Pain and Disability in Patients with Lumbar Disc Protrusion. Is Early Intervention the Best Recommendation?

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200422047172N2
Enrollment
60
Registered
2022-03-21
Start date
2021-07-21
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

Low back pain. Other intervertebral disc disorders, lumbar region

Interventions

Intervention 1: Intervention group 1/Experimental group: 30 patients received a complex individualized physical therapy (PT) program associated with hydro-therapy(HT) and electrotherapy (ET). Hydroth
2) Interferential current (IFC) in quadripolar mode, at 100 Hz frequency, for 10 min
3) Magnetic field therapy in continuous form (sedative effect), for 15 min. TENS and IFC were performed using the Chattanooga Intelect Neo combined de-vice. The magnetic field was delivered through a

Sponsors

Department of Physical Education, Sport and Physiotherapy, University of Oradea
Lead Sponsor

Eligibility

Sex/Gender
All
Age
26 Years to 76 Years

Inclusion criteria

Inclusion criteria: 25-80?years of age low back pain for more than three months MRI confirmed diagnosis of lumbar disc protrusion (without dural compression) ability to perform a physical therapy program

Exclusion criteria

Exclusion criteria: indication for acute surgery previous surgery on the same lumbar spinal level sciatica presence of severe spinal pathology (spinal tumour, spinal fracture, spinal stenosis or radiculopathy, fibromyalgia, inflammatory and infectious spinal diseases) chronic use of pain killer drugs refusal to participate in the research neoplasms of any sort, severe comorbidities mental illness refusal to participate in the research

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: before intervention and 6 months after intervention. Method of measurement: Short Form McGill Pain Questionnaire (SF-MPQ) and visual analogue scale (VAS).;Disability. Timepoint: before intervention and 6 months after intervention. Method of measurement: Oswestry Disability Index (ODI).

Countries

Romania

Contacts

Public ContactElena Sirbu

West University of Timisoara

elena.sirbu@e-uvt.ro+40 744 238 960

Outcome results

None listed

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