ClinicalTrials.Veeva

Menu

Effects of a Prehabilitation Program in Patients Undergoing Lumbar Radiculopathy Surgery

C

Cardenal Herrera University

Status

Not yet enrolling

Conditions

Lumbar Radiculopathy

Treatments

Other: Physiotherapy

Study type

Interventional

Funder types

Other

Identifiers

NCT06145620
CEEI23/459

Details and patient eligibility

About

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.

Full 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.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

100 participants in 2 patient groups

Therapeutic exercise, back care and pain neuroscience education group
Experimental group
Treatment:
Other: Physiotherapy
Standarized written exercise group
Active Comparator group
Treatment:
Other: Physiotherapy

Trial contacts and locations

1

Loading...

Central trial contact

María Dolores Arguisuelas; María Dolores Arguisuelas

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems