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A comparison between the effects of dynamic thoracic stabilization exercise and lumbar in women with chronic non-specific low back pain

A comparison between the effects of dynamic thoracic stabilization exercise and lumbar on the activity of trunk muscles, pain and disability in women with chronic non-specific low back pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20090210001675N14
Enrollment
30
Registered
2018-11-30
Start date
2017-08-23
Completion date
Unknown
Last updated
2019-01-14

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. Dorsalgia, unspecified

Interventions

Intervention 1: Intervention group: dynamic thoracic stabilization exercise, eighteen training sessions during 6 consecutive weeks, three times per week, 30 or 40 minutes per session including: Twenty

Sponsors

Zahedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Nonspecific LBP for a period of at least 3 months; women aged over 18 and less than 55 years old; no history of musculoskeletal disorders in hip and lower extremities; no history of radicular pain, spinal stenosis, any neurologic sign, systemic infection, cardiovascular and balance disorders, severe deformity of musculoskeletal injury to the leg or medication one week before the test session; not pregnant; no history of diabetes, respiratory disorders, spinal surgery, nerve root pain, severe spinal deformity or disease; no history of metabolic, systemic, inflammatory diseases, arthritis and malignancies.

Exclusion criteria

Exclusion criteria: Patients who were absent more than three consecutive sessions of treatment; patients who doing exercises aggravated their pain; receiving or doing other therapies during the study.

Design outcomes

Primary

MeasureTime frame
Trunk muscles activity. Timepoint: Before intervention and 6 weeks after intervention. Method of measurement: Electromyography.;Pain. Timepoint: Before intervention and 6 weeks after intervention. Method of measurement: Visual Analogue Scale.;Functional disability. Timepoint: Before intervention and 6 weeks after intervention. Method of measurement: Oswestery scale.

Secondary

MeasureTime frame
No secondary outcome. Timepoint: no secondary outcome. Method of measurement: no secondary outcome.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAsghar Akbari

Zahedan University of Medical Sciences

akbari_as@yahoo.com+98 54 3342 4675

Outcome results

None listed

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