Dynamic Lumbar Strengthening Exercises Versus Pilates, Combined With Myofascial Release in Non Specific Chronic Low Back Pain
1 other identifier
interventional
60
1 country
1
Brief Summary
This randomized controlled trial aims to compare the effectiveness of dynamic lumbar strengthening exercises combined with myofascial release versus Pilates combined with myofascial release in individuals with non-specific chronic low back pain. Non-specific chronic low back pain is one of the most common musculoskeletal disorders affecting adults and is associated with pain, reduced spinal mobility, and functional disability. Exercise-based rehabilitation programs and manual therapy techniques are commonly used to improve functional outcomes in these patients. Dynamic lumbar strengthening exercises focus on improving spinal stability and strengthening trunk musculature, whereas Pilates exercises emphasize core muscle activation, postural control, and controlled movement patterns. Myofascial release is a manual therapy technique used to reduce fascial restrictions, improve soft tissue mobility, and decrease pain. In this randomized controlled trial, a total of 60 participants aged between 25 and 35 years with non-specific chronic low back pain lasting more than three months will be recruited from the Physiotherapy Department of the University of Lahore Teaching Hospital. Participants will be randomly allocated into two groups. Group A will receive dynamic lumbar strengthening exercises combined with myofascial release, while Group B will receive Pilates exercises combined with myofascial release. Both groups will also receive baseline therapy consisting of therapeutic massage, interferential therapy, and therapeutic ultrasound applied to the lumbosacral region. The exercise programs will be conducted for eight weeks on alternate days, with each session lasting approximately 20-25 minutes. Outcome measures will include pain intensity assessed using the Visual Analog Scale (VAS), functional disability measured using the Oswestry Disability Index (ODI), and lumbar range of motion measured using an inclinometer. Assessments will be conducted at baseline before the intervention and after completion of the 8-week intervention period. The findings of this study will help determine which exercise approach combined with myofascial release is more effective in reducing pain, improving functional disability, and enhancing spinal mobility in individuals with non-specific chronic low back pain. The results may contribute to evidence-based physiotherapy management and improve rehabilitation strategies for patients with chronic low back pain.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2026
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
First Submitted
Initial submission to the registry
March 9, 2026
CompletedFirst Posted
Study publicly available on registry
March 13, 2026
CompletedStudy Start
First participant enrolled
March 19, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 19, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 20, 2026
CompletedMarch 17, 2026
March 1, 2026
2 months
March 9, 2026
March 15, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pain Intensity Measured by Visual Analog Scale (VAS)
Pain intensity will be assessed using the Visual Analog Scale (VAS). The VAS consists of a 10-cm horizontal line anchored with two descriptors: "no pain" at 0 and "worst imaginable pain" at 10. Participants will mark their perceived pain intensity on the line, and the score will be recorded in centimeters to quantify pain severity.
Baseline, 2 weeks and after 8 weeks
Study Arms (2)
group A Dynamic Lumbar Strengthening Exercises with Myofascial Release
EXPERIMENTALParticipants in this group will receive dynamic lumbar strengthening exercises combined with myofascial release therapy for the management of non-specific chronic low back pain. The exercise program will include bird dog, glute bridge, dead bug, side-lying leg lifts, and modified superman exercises performed on a mat. Each session will last approximately 20-25 minutes and will be conducted on alternate days for 8 weeks under the supervision of a physiotherapist. Myofascial release techniques will be applied to the thoracolumbar fascia using sustained pressure, longitudinal gliding, and fascial stretching techniques for approximately 4-6 minutes per session. Participants will also receive baseline therapy including therapeutic massage, interferential therapy, and therapeutic ultrasound applied to the lumbosacral region.
group B Pilates Exercises with Myofascial Release
ACTIVE COMPARATORParticipants in this group will receive Pilates-based exercises combined with myofascial release therapy for the treatment of non-specific chronic low back pain. The Pilates program will focus on core stabilization, breathing control, and spinal mobility. Exercises will include pelvic tilts, pelvic curl, modified hundred, single-leg stretch, swimming, and knee folds performed on a mat. Each session will last approximately 20-25 minutes and will be conducted on alternate days for a period of 8 weeks under physiotherapist supervision. Myofascial release techniques will be applied to the thoracolumbar fascia using standardized manual techniques for approximately 4-6 minutes per session. Participants will also receive baseline therapy including therapeutic massage, interferential therapy, and therapeutic ultrasound applied to the lumbosacral region.
Interventions
Dynamic lumbar strengthening exercises will be performed to improve spinal stability and strengthen trunk musculature in individuals with non-specific chronic low back pain. The exercise program will include bird dog, glute bridge, dead bug, side-lying leg lifts, and modified superman exercises. Sessions will be conducted on a mat under the supervision of a physiotherapist. Each session will last approximately 20-25 minutes and will be performed on alternate days for a total duration of 8 weeks. Exercise intensity and repetitions will be gradually progressed according to the participant's tolerance while maintaining correct posture and controlled movement.
Participants will receive Pilates-based exercises combined with myofascial release therapy for the treatment of non-specific chronic low back pain. The Pilates program will focus on core muscle activation, breathing control, and spinal mobility. Exercises will include pelvic tilts, pelvic curl (bridge), modified hundred, single-leg stretch, swimming exercise, and knee folds performed on a mat under physiotherapist supervision. Each session will last approximately 20-25 minutes and will be conducted on alternate days for 8 weeks. Myofascial release techniques will be applied to the thoracolumbar fascia using standardized manual therapy techniques for approximately 4-6 minutes per session
Eligibility Criteria
You may qualify if:
- Male and female aged between 25 to 35 years. History of persistent low back pain for more than 3 months. Pain intensity with a score \> 3 on the Visual Analog Scale (VAS). Functional disability measured by the Oswestry Disability Index (ODI), with scores ranging from 20% to 60%
You may not qualify if:
- Individuals with acute or subacute low back pain. Presence of systemic illnesses or specific spinal pathologies. Psychological disorders such as severe anxiety or depression affecting participation.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Maheen Rauflead
Study Sites (1)
University of Lahore Teaching Hospital, Lahore
Lahore, Punjab Province, 54000, Pakistan
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Maheen Rauf, MS MSK
The University of Lahore, Lahore
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- principal investigator
Study Record Dates
First Submitted
March 9, 2026
First Posted
March 13, 2026
Study Start
March 19, 2026
Primary Completion
May 19, 2026
Study Completion
May 20, 2026
Last Updated
March 17, 2026
Record last verified: 2026-03