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Comparative Effects of Core Stability and Postural Control Training on chronic non-specific low back pain

Comparative Effects of Core Stability and Postural Control Training on Pain, Disability, and Sensorimotor Function in Women with Chronic Non-Specific Low Back Pain: A Three-Armed Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250519065806N2
Enrollment
51
Registered
2026-04-12
Start date
2026-09-06
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Chronic non-specific low back pain. Lordosis, unspecified, lumbar region

Interventions

Intervention 1: Intervention group: After obtaining ethical approval, middle-aged women with chronic non-specific low back pain (CNSLBP) who met the study inclusion criteria were invited to participat

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to 57 Years

Inclusion criteria

Inclusion criteria: female sex middle age (40-57) chronic non-specific low back pain for more than three months absence of specific spinal pathology or musculoskeletal disoredrs approved chronic non-specific low back pain by doctor of medicine Willingness to participate in the intervention and written informed consent Pain intensity of at least 3 out of 10 based on the visual analog scale No participation in structured rehabilitation or corrective exercise programs during the previous three months.

Exclusion criteria

Exclusion criteria: History of spinal surgery Presence of specific spinal disorders such as: lumbar disc herniation, spondylolisthesis, spinal stenosis Presence od radiculopathy or radiating pain to the lower limbs Neurological or vestibular disorders affecting balance or motor control Musculoskeletal injury in the lower extrimities during the past six months Pregnancy or planning to become pregnant during the study period absence from more than two exercise sessions during the interventional period

Design outcomes

Primary

MeasureTime frame
Pain intensity, Functional disability, Lumbo-pelvic proprioception, Static balance, Quality of life (QOL). Timepoint: First week and 8 weeks. Method of measurement: Visual Analog Scale (VAS), Oswestry Disability Index, Roland–Morris Disability Questionnaire, joint position reproduction test (Goniometer), Stork Stand Test, Short form SF-36 questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad-Ali Seyed-Hoseini

Islamic Azad University

ahoseini78@ut.ac.ir+98 21 8837 2567

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026