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Investigating the effect of walking on postural reactions in patients with low back pain

Investigating the effect of walking on postural reactions, pain and disability in patients with non-specific chronic low back pain

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180714040466N7
Enrollment
30
Registered
2023-10-09
Start date
2023-10-23
Completion date
Unknown
Last updated
2023-10-16

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: Control group: Electrotherapy includes 20 minutes of TENS, 20 minutes of infrared, stretching and strengthening exercises, and active free exercise for lumbosacral. The total duration

Sponsors

Zahedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Years: Range:18-45, males and females Chronic back pain in the area between the twelfth rib and the rump without reference to the lower limbs, which has lasted for more than three months and has no specific cause and has caused problems in performance and physical disability and has not subsided. People with a desire to enter the study

Exclusion criteria

Exclusion criteria: History of neurological disorder Rheumatic diseases Cancer Spinal cord lesions History of surgery Structural injuries of the spine Pregnancy History of therapeutic exercise in the last 3 months

Design outcomes

Primary

MeasureTime frame
1-Overall static stability index. Timepoint: The beginning of the study (before the start of the intervention) and the end of the 6-week treatment period. Method of measurement: Biodex device.;Anterior-posterior static stability index. Timepoint: The beginning of the study (before the start of the intervention) and the end of the 6-week treatment period. Method of measurement: Biodex device.;Internal and external static stability index. Timepoint: The beginning of the study (before the start of the intervention) and the end of the 6-week treatment period. Method of measurement: Biodex device.;Overall dynamic stability index. Timepoint: The beginning of the study (before the start of the intervention) and the end of the 6-week treatment period. Method of measurement: Biodex device.;Anterior-posterior dynamic stability index. Timepoint: The beginning of the study (before the start of the intervention) and the end of the 6-week treatment period. Method of measurement: Biodex device.;Stability index of internal and external dynamics. Timepoint: The beginning of the study (before the start of the intervention) and the end of the 6-week treatment period. Method of measurement: Biodex device.;Pain intensity index. Timepoint: The beginning of the study (before the start of the intervention) and the end of the 6-week treatment period. Method of measurement: VAS questionnaire.;Disability severity index. Timepoint: The beginning of the study (before the start of the intervention) and the end of the 6-week treatment period. Method of measurement: Oswestry Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFateme Ghiasi

Zahedan University of Medical Sciences

f_ghiasi_p@zaums.ac.ir+98 54 3322 0501

Outcome results

None listed

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