Actively Recruiting

Phase Not Applicable
Age: 18Years - 55Years
All Genders
NCT07030582

Efficacy of Internet-Based Cognitive Behavioral Therapy for Back Muscle Strength Loss, Chronic Pain, and Poor Patient Recovery Perceptions After Lumbar Fusion

Led by Jiawei Jiang · Updated on 2025-06-22

100

Participants Needed

1

Research Sites

213 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to develop an Internet-based Cognitive Behavioral Therapy protocol for core muscle training, based on an understanding of factors impeding postoperative core muscle training in lumbar surgery patients. The protocol is designed to reconstruct patients' cognition, eliminate adverse behaviors, and promote healthy behaviors such as core muscle training among LDH patients. The ultimate objectives are to alleviate postoperative pain, enhance lumbar stability, and facilitate disease rehabilitation in patients following lumbar surgery.

CONDITIONS

Official Title

Efficacy of Internet-Based Cognitive Behavioral Therapy for Back Muscle Strength Loss, Chronic Pain, and Poor Patient Recovery Perceptions After Lumbar Fusion

Who Can Participate

Age: 18Years - 55Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 55 years
  • Diagnosis of lumbar disc herniation requiring single-level lumbar fusion surgery
  • No previous history of lumbar surgery
  • Surgical procedures performed by the same surgical team
  • Willingness to comply with the study protocol and restrictions
  • Availability of a home WiFi connection
Not Eligible

You will not qualify if you...

  • Lumbar surgery secondary to neoplasm, tuberculosis, infection, or inflammation
  • Postoperative infection or revision surgery
  • Presence of cauda equina syndrome
  • Diagnosis of schizophrenia, cognitive impairment, or other psychiatric disorders
  • Coexisting severe cardiovascular or cerebrovascular diseases, or congenital conditions precluding exercise participation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Affiliated 2 Hospital of Nantong University

Nantong, Jiangsu, China, 0513

Actively Recruiting

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Research Team

T

Tingting Wang

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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