Effects of a Prehabilitation Program in Patients Undergoing Lumbar Radiculopathy Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorCardenal Herrera University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

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.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Physiotherapy

    Other intervention

    The intervention involves the visualization of different videos explaining the performance of lumbar strengthening exercises, measures for back care, and neuroscience pain education.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Therapeutic exercise, back care and pain neuroscience education groupExperimental treatment 1 intervention
Group B: Standarized written exercise groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Oswestry Disability Index (ODI)

Disability score (0-100). Higher score indicates higher disability.

Time frame
4 weeks

Secondary outcomes

1

SF-McGill Pain Questionnaire (SF-MGPQ)

Pain score (0-45). Higher score indicates higher pain level

Time frame
4 weeks
2

Numerical Rating Scale (NRS)

Pain score 0-10. Higher score indicates higher pain intensity.

Time frame
4 weeks
3

EuroQol-5D (EQ-5D)

Quality of life score (-0.5 to 1).Higher score indicates higher health-related quality of life

Time frame
4 weeks
4

Fear avoidance beliefs questionnaire (FABQ)

FABQ-Work subscale (ranging from 0 to 42) and FABQ-Physical Activity subscale (ranging from 0 to 24). Higher score indicates more signs of fear avoidance

Time frame
4 weeks

Other outcomes

Sponsors and contacts

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