The Influence of the Timing of Postoperative Rehabilitation Intervention on the Clinical Efficacy of Unilateral Biportal Endoscopic Spine System in the Treatment of Lumbar Disc Herniation

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age19-65
SponsorLi Xiang

About this trial

This study focuses on the impact of the timing of postoperative rehabilitation intervention on the clinical efficacy of unilateral biportal endoscopic spine surgery in the treatment of lumbar disc herniation. The main objective is to explore this impact and provide high-quality evidence-based medical evidence for making reasonable clinical decisions.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged between 19 and 65 years.

Disqualifiers

Aged under 18 or over 65 years.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Standardized Postoperative Rehabilitation Protocol

    Behavioral

    This intervention is a standardized, progressive rehabilitation protocol for patients after lumbar disc herniation surgery, delivered under the guidance of a senior physical therapist. The protocol aims to improve pain, restore function, and prevent complications through core stability exercises and neurodynamic techniques. The exercises are performed once daily and progressed based on patient tolerance. The protocol consists of two phases: Initial Phase ( commencing postoperatively): Includes: 1) Transverse abdominis activation; 2) Sit-to-stand training with abdominal bracing; 3) Four-point kneeling rockbacks for spinal mobility; 4) Neural mobilization techniques (performed in sitting); 5) Neural sliding techniques (performed in sitting). Progressive Phase: Builds upon the initial exercises by increasing the range of motion, adding isometric hold times, and integrating cervical movement with neural techniques to increase difficulty and intensity.

Treatment groups

72 Participants
are divided into 2 treatment groups
Group A: Early Rehabilitation GroupExperimental treatment 1 intervention
Group B: Late Rehabilitation GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Oswestry Disability Index (ODI) Score

The Oswestry Disability Index (ODI) is a widely validated and disease-specific patient-reported outcome measure for assessing functional status in individuals with low back pain. The questionnaire consists of 10 items addressing pain intensity, personal care, lifting, walking, sitting, standing, sleeping, social life, traveling, and employment/homemaking. Each item is scored from 0 to 5, and the total score is converted to a percentage (0-100%), with higher scores indicating greater disability. The ODI score at 12 months postoperatively will be used as the primary endpoint to evaluate the long-term effect of rehabilitation timing.

Time frame
Change from Baseline to 12 months postoperatively

Secondary outcomes

Other outcomes

Sponsors and contacts

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Li Xiang

Lead sponsor

Beijing Friendship Hospital

Sponsor institution