CompletedNot Applicable

Rehabilitation Interventions for Postoperative Degenerative Lumbar Disease

Taiwan90 participantsStarted 2024-12-01

Plain-language summary

The purpose of this study is to evaluate the effects of different rehabilitation interventions on patients who have undergone surgery for degenerative lumbar disease. The study focuses on assessing improvements in neuropathic pain, functional recovery, and overall quality of life. Participants will be randomly assigned to different rehabilitation programs to determine which approach provides the best outcomes for postoperative recovery.

Who can participate

Age range20 Years – 80 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients diagnosed by a neurosurgeon with lumbar spinal stenosis, spondylolisthesis, or spondylosis involving L2-S1 segments, and scheduled for lumbar spine surgery. * First-time recipients of lumbar spine surgery. * Adults who are conscious and able to communicate effectively in Mandarin/Taiwanese (verbally or through writing). * No history of psychiatric disorders. * Willing to participate and sign the informed consent form. Exclusion Criteria: * Lower back pain caused by infection, inflammation, or malignancy (cancer). * History of previous lumbar spine surgery. * Patients with substance or drug addiction. * Presence of psychiatric disorders. * Unable to communicate effectively.

What they're measuring

Change From Baseline in Taiwan Version of Neuropathic Pain Symptom Inventory (NPSI-T) Score

Timeframe: Baseline, 1 week, 2 weeks, 4 weeks, and 8 weeks post-surgery.

Trial details

NCT IDNCT07550660

SponsorNational Taiwan University Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-06-27

View on ClinicalTrials.gov More Degenerative Lumbar Disease trials