Core Stability Training in Young Adults With Chronic Non-Specific Low Back Pain
Effects of Core Stability Training on Functional Recovery in Young Adults With Chronic Non-Specific Low Back Pain
1 other identifier
interventional
30
1 country
1
Brief Summary
Chronic non-specific low back pain is common among young adults and can lead to persistent pain, reduced physical function, decreased muscle strength, and impaired balance, affecting daily activities and quality of life. Core stability exercises are widely used in rehabilitation programs for low back pain, but the effectiveness of Swiss ball-based core stability training in young adults with chronic non-specific low back pain remains unclear. The purpose of this study is to investigate whether Swiss ball-based core stability training can reduce pain and improve functional recovery in young men with chronic non-specific low back pain compared with conventional mat-based lumbar muscle exercises. Participants will be randomly assigned to either a Swiss ball core stability training group or a mat-based lumbar muscle training group and will complete a 6-week exercise intervention program. The study will evaluate changes in pain intensity, disability related to low back pain, lumbar muscle strength, and dynamic balance ability. The study hypothesizes that Swiss ball-based core stability training will produce greater improvements in pain relief, physical function, muscle strength, and balance than conventional mat-based lumbar muscle exercises.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jan 2021
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2021
CompletedFirst Submitted
Initial submission to the registry
June 30, 2026
CompletedFirst Posted
Study publicly available on registry
July 7, 2026
CompletedJuly 7, 2026
June 1, 2026
2 months
June 30, 2026
June 30, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Pain intensity
Pain intensity will be assessed using the Visual Analog Scale (VAS). Participants will rate their current level of low back pain on a 10-cm scale ranging from 0 to 10, where 0 represents "no pain" and 10 represents "the worst pain imaginable." Higher scores indicate greater pain intensity.
From enrollment to the end of treatment at 6 weeks
Low back disability
Low back-related disability will be assessed using the Oswestry Disability Index (ODI), a widely used measure of functional impairment associated with low back pain. The questionnaire consists of 10 items evaluating the impact of low back pain on activities of daily living. Each item is scored from 0 to 5, and the total score is converted into a percentage, with higher scores indicating greater disability.
From enrollment to the end of treatment at 6 weeks
Secondary Outcomes (2)
Lumbar muscle strength
From enrollment to the end of treatment at 6 weeks
Dynamic balance ability
From enrollment to the end of treatment at 6 weeks
Study Arms (2)
Swiss ball-based core stability training
EXPERIMENTALParticipants in this arm will perform core stability training using a Swiss ball as the primary exercise equipment. Before the formal training session, participants will complete a 5-minute supervised warm-up consisting of dynamic stretching exercises focusing on the spine, shoulders, and hips, together with light running and jumping activities for the lower extremities. The core stability program consists of six exercise components performed in a progressive sequence from easier to more difficult tasks, with gradual reductions in the base of support to increase instability and challenge trunk control. As participants adapt to the intervention over time, the training load will be periodically increased to optimize therapeutic effects. Following each training session, participants will complete 5 minutes of static stretching exercises as a cool-down activity.
Mat-based lumbar muscle exercises
ACTIVE COMPARATORParticipants in this arm will perform lumbar muscle exercises using a mat as the primary exercise surface. Apart from the exercise equipment used, the overall training protocol will be identical to that of the Swiss ball-based core stability training group. Before the formal training session, participants will complete the same 5-minute supervised warm-up program consisting of dynamic stretching exercises and light running and jumping activities. After each training session, participants will also perform 5 minutes of static stretching exercises as a cool-down activity.
Interventions
Participants in this arm will perform core stability training using a Swiss ball as the primary exercise equipment. Before the formal training session, participants will complete a 5-minute supervised warm-up consisting of dynamic stretching exercises focusing on the spine, shoulders, and hips, together with light running and jumping activities for the lower extremities. The core stability program consists of six exercise components performed in a progressive sequence from easier to more difficult tasks, with gradual reductions in the base of support to increase instability and challenge trunk control. As participants adapt to the intervention over time, the training load will be periodically increased to optimize therapeutic effects. Following each training session, participants will complete 5 minutes of static stretching exercises as a cool-down activity.
Participants in this arm will perform lumbar muscle exercises using a mat as the primary exercise surface. Apart from the exercise equipment used, the overall training protocol will be identical to that of the Swiss ball-based core stability training group. Before the formal training session, participants will complete the same 5-minute supervised warm-up program consisting of dynamic stretching exercises and light running and jumping activities. After each training session, participants will also perform 5 minutes of static stretching exercises as a cool-down activity.
Eligibility Criteria
You may qualify if:
- Male participants aged 18 to 25 years.
- Diagnosis of chronic non-specific low back pain characterized by pain or discomfort located between the lower rib margin and the gluteal folds, with or without lower limb pain.
- No signs of nerve root compression and a negative straight leg raise test.
- No identifiable specific pathological or anatomical cause of low back pain.
- Baseline pain intensity score greater than 2 and less than 9 on the Visual Analog Scale (VAS).
- Duration of low back pain symptoms longer than 12 weeks.
- No treatment for low back pain received within the previous month.
- Willingness to participate in the study and provide written informed consent.
You may not qualify if:
- Failure to meet the diagnostic criteria for chronic non-specific low back pain.
- History of spinal trauma or spinal surgery.
- Presence of severe cardiovascular diseases, such as uncontrolled hypertension.
- Presence of severe metabolic diseases, such as gout.
- Presence of severe infectious diseases, such as pneumonia.
- Diagnosed structural spinal disorders, including lumbar disc herniation, spondylolisthesis, spinal stenosis, or other identifiable pathological anatomical abnormalities.
- Any medical condition that would prevent safe participation in the exercise intervention as determined by the investigators.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Guangxi Normal University
Guilin, Guangxi, 541004, China
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- CARE PROVIDER, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 30, 2026
First Posted
July 7, 2026
Study Start
January 1, 2021
Primary Completion
March 1, 2021
Study Completion
March 1, 2021
Last Updated
July 7, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will not share