Effects of a Prehabilitation Program Based on Therapeutic Exercise, Back Care Education and Neuroscience Pain Education in Patients Undergoing Lumbar Radiculopathy Surgery
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 100
- Locations
- 1
- Primary Endpoint
- Oswestry Disability Index (ODI)
Study Overview
Brief Summary
The purpose of the following study is to analyze the effects of a prehabilitation program based on therapeutic exercise, back care education and pain neuroscience education through the visualization of videos, compared to standardized written therapeutic exercise in patients undergoing lumbar radiculopathy surgery.
Detailed Description
So far, there are no previous studies that analyze the effects of a prehabilitation program including therapeutic exercise, back care education and pain neuroscience education through the visualization of videos in patients undergoing lumbar radiculopathy surgery.
This is a multicenter randomized clinical trial aimed at analyzing the effects of a 4 weeks prehabilitation program based on video visualization versus the performance of standardized written exercises in patients undergoing lumbar radiculopathy surgery.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Investigator)
Eligibility Criteria
- Ages
- 18 Years to 80 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Adults aged 18 years or older, diagnosed with lumbar radiculopathy, and scheduled for surgery. The symptoms will be predominantly leg pain with or without neurological deficit, with surgical decompression justified.
Exclusion Criteria
- •Patients currently receiving any other non-pharmacological treatment or physical therapy for the management of lumbar radiculopathy.
- •Proposed for surgery with instrumentation (e.g., spinal fusion, arthrodesis).
- •Suffering from a chronic pain-related condition (e.g., fibromyalgia, chronic fatigue syndrome).
- •Symptoms of spinal cord compression.
- •Diagnosed with a malignant tumor.
- •Mental illness.
- •Previously undergone spinal surgery.
- •No access to any internet-enabled device.
Outcomes
Primary Outcomes
Oswestry Disability Index (ODI)
Time Frame: 4 weeks
Disability score (0-100). Higher score indicates higher disability.
Secondary Outcomes
- Pain catastrophizing scale (PCS)(4 weeks)
- SF-McGill Pain Questionnaire (SF-MGPQ)(4 weeks)
- International Physical Activity Questionnaire (IPAQ)(4 weeks)
- Numerical Rating Scale (NRS)(4 weeks)
- EuroQol-5D (EQ-5D)(4 weeks)
- Hospital Anxiety and Depression Scale (HADS)(4 weeks)
- Tampa scale for kinesiophobia (TSK-11SV)(4 weeks)
- Fear avoidance beliefs questionnaire (FABQ)(4 weeks)
Investigators
ARGUISUELAS MARTINEZ MARÍA DOLORES
Professor
Cardenal Herrera University