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Effect of lumbosacral orthosis on non-specific chronic low back pain

Effect of Extensible and non-Extensible Lumbosacral Orthoses on the Flexion Relaxation Phenomenon in Patients with Chronic non-Specific Low Back Pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200315046784N2
Enrollment
40
Registered
2022-06-17
Start date
2022-06-19
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

non-specific chronic low back pain. Low back pain

Interventions

Intervention 1: Intervention group: Group A will be received an extensible lumbosacral orthosis. The patients will be asked to wear the orthosis all day long for 4 weeks. Intervention 2: Intervention

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: age 18 to 65 yrs history of LBP for at least 12 weeks pain intensity of at least 3 on VAS a score of at least 12% on the ODI Standing and walking without assistance not receiving orthosis, kinesio-tape and or physical therapy for the last 3 months

Exclusion criteria

Exclusion criteria: neurological symptoms due to nerve root compression severe spinal deformities history of spinal or abdominal surgery systemic diseases neuromuscular diseases BMI of more than 30 Antidepressive, Anxiolytic, Anticonvulsant drugs

Design outcomes

Primary

MeasureTime frame
Disability score on Oswestry Disability Index. Timepoint: before and after 4 weeks intervention. Method of measurement: Oswestry Disability Index.;Pain intensity. Timepoint: before and after 4 weeks intervention. Method of measurement: Visual analogue scale.

Secondary

MeasureTime frame
Fear of movement (kinesiophobia). Timepoint: before and after 4 weeks intervention. Method of measurement: Tampa Scale of Kinesiophobia.;Back muscle endurance. Timepoint: before and after 4 weeks intervention. Method of measurement: Biering-Sørensen Test.;Flexion relaxation ratio. Timepoint: before and after 4 weeks intervention. Method of measurement: electromyography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Azadinia

Iran University of Medical Sciences

azadinia.fatemeh@yahoo.com+98 21 2222 8051

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026