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

Trunk and Lower Limb Movement Quality and Stability Improvement in People With Chronic Low Back Pain Following Different Types of Isometric Trunk Muscle Training

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06944730
Acronym
CLBP
Enrollment
60
Registered
2025-04-25
Start date
2022-06-01
Completion date
2025-11-30
Last updated
2025-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Low Back Pain (CLBP)

Keywords

movement quality, balance, trunk muscle training

Brief summary

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.

Detailed description

Both ITE and SE training are equalized in terms of training intensity based on rate of perceived exertion, training duration per session, training frequency, and intervention period. Training intensity measurement does not use other methods of quantification as ITE training does not increase heart rate or blood lactate significantly regardless of the intensity.

Interventions

Multi-joint limb movement with force vector through the spine. The spine is held at neutral position

BEHAVIORALIsolated Trunk Exercise

Holding the spine in neutral position with no limb movement, with static loading through the spine

BEHAVIORALBack school

Patient education that has been proven to not be effective and has been used as control in past low back pain intervention studies

Sponsors

The Hong Kong Polytechnic University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* body mass index (BMI) 18-25 kg/m2 * experiencing intermittent pain lasting at least 3 months * had Oswestry Disability Index (ODI) score ranging between 17% and 45%.

Exclusion criteria

* exercise contraindication based on physical activity readiness questionnaire * indication or diagnosis of other chronic diseases (such as cancer, cardiovascular disease, diabetes, bone fracture, or infection) * artificial lower limb joints, history of spinal surgery, walking aid use * personal mobility restrictions (due to connective tissue diseases, rheumatoid arthritis, or central nervous system disorders) * pregnancy or within 1 year post partum

Design outcomes

Primary

MeasureTime frameDescription
5RSTS timeSame day as first day of intervention and within one week after interventionTime required to complete five-repetitions sit-to-stand with smaller time indicating better performance.
Perceived painSame day as first day of intervention and within one week after interventionscore from numerical pain rating scale from zero (0) to ten (10), with 0 indicating no pain.
Perceived disabilitySame day as first day of intervention and within one week after interventionScore based on oswestry disability index scoring from zero (0) to one hundred (100) percent, with zero indicating no disability.
Lower lumbar active range of motionSame day as first day of intervention and within one week after interventionactive range of motion of the lower lumbar area during five-repetitions sit-to-stand test.
Segmental movement coordinationSame day as first day of intervention and within one week after interventionLumbar-to-pelvis and pelvis-to-femur movement coordination as quantified by mean absolute relative phase angle during five-repetitions sit-to-stand. Smaller number indicates greater coordination between the two segments.
Segmental movement stabilitySame day as first day of intervention and within one week after interventionlumbar-to-pelvis and pelvis-to-femur movement stability as quantified by deviation phase during five-repetitions sit-to-stand. Greater number indicates lesser segmental movement stability.
Postural stabilitySame day as first day of intervention and within one week after interventionCenter-of-pressure normalized mean velocity during Y-balance test. Smaller number indicate greater stability
Postural ControlSame day as first day of intervention and within one week after interventionnormalized leg reach during y-balance test, with larger number indicating greater postural control.

Secondary

MeasureTime frameDescription
Muscle synergySame day as first day of intervention and within one week after interventionMuscle synergy as measured by the surface electromyography (SEMG) output of the latissimus dorsi, longissimus pars thoracis, longissimus pars lumborum, external oblique, rectus abdominis, gluteus maximus and biceps femoris muscle both on left and right side during all functional tests. SEMG signals would then be processed using non-negative matrix factorization to find the underlying muscle synergies
LAP performanceSame day as first day of intervention and within one week after interventiontime required to complete the lift and place test with lesser time indicating greater performance

Countries

Hong Kong

Contacts

Primary ContactDhananjaya Sutanto, Ph.D.
dhananjaya.sutanto@polyu.edu.hk+852 9680 7397

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026