Actively Recruiting

Phase Not Applicable
Age: 18Years - 55Years
All Genders
NCT06944730

Movement Quality and Balance Improvement in People With Chronic Low Back Pain Following Trunk Muscle Training

Led by The Hong Kong Polytechnic University · Updated on 2025-04-25

60

Participants Needed

1

Research Sites

182 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this project is to assess if Chronic Low Back Pain (CLBP) participant's movement quality and balance variables can change after training that decreases their pain and disability. It will also compare the difference between structural exercise (SE) and isolated trunk exercise (ITE). The main questions it aims to answer are: 1. What are the effect of the training on the participant's movement quality and balance. 2. What are the difference between different types of trunk muscle training on people with CLBP. Researchers will compare SE, ITE and control. Control group will receive back school education that was shown not to be effective in reducing pain and disability. Participants will: 1. Do home and in-lab based SE or ITE training, or maintain active daily living over 2 months. 2. Complete the pain and disability questionnaire and do several physical functioning tests while having their trunk and lower limb movement and muscle activation measured.

CONDITIONS

Official Title

Movement Quality and Balance Improvement in People With Chronic Low Back Pain Following Trunk Muscle Training

Who Can Participate

Age: 18Years - 55Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Body mass index (BMI) between 18 and 25 kg/m2
  • Experiencing intermittent low back pain lasting at least 3 months
  • Oswestry Disability Index (ODI) score between 17% and 45%
Not Eligible

You will not qualify if you...

  • Exercise contraindications based on physical activity readiness questionnaire
  • Diagnosis or indication of other chronic diseases such as cancer, cardiovascular disease, diabetes, bone fracture, or infection
  • Having artificial lower limb joints, history of spinal surgery, or use of walking aid
  • Personal mobility restrictions due to connective tissue diseases, rheumatoid arthritis, or central nervous system disorders
  • Being pregnant or within 1 year postpartum

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

The Hong Kong Polytechnic University

Hong Kong, Hong Kong

Actively Recruiting

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Research Team

D

Dhananjaya Sutanto, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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