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the effect of education in treatment of chronic low back pain

The effect of adding pain neuroscience education on the clinical results of core muscle training using pressure biofeedback in people with chronic low back pain diagnosed with functional instability

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240916063057N1
Enrollment
48
Registered
2024-10-20
Start date
2024-11-17
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

chronic low back pain diagnosed with functional instability.

Interventions

Intervention 1: Intervention group: core muscle training using pressure biofeedback device along with pain neuroscience education. Intervention 2: Control group: core muscle training using pressure bi

Sponsors

University of social welfare and rehabilitation sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: age range 18-40 at least education level is diploma prone instability test is positive Gower’s sign is positive at least 3 month patient have continuous pain in lumbago there is no obvious symptom in lumbar region ( patients rule out when have these disorder: decrease sensation in specific dermatome , decrease strength in specific myotome of lumbar region , disc herniation ,sacroiliac joint dysfunction ) at least patient have 3times low back pain during last year intensity of patient's pain during Gower’s test in Visual Analogous Scale should be 3to7 Oswestry disability index more than 12% patient can stand and walk without any supportive aid such as cane patient don't have Rheumatoid and central nervous system disorder patient don't have any history of tumor, malignancy and spinal malposture patient don't have any history of abdominal surgery at least score of MMSE for measuring cognition state should be 27 BMI not more than 30 patient don't get any medications and exercise therapy during last 3 month

Exclusion criteria

Exclusion criteria: pregnancy sitting more than 2 hours a day

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: pre treatment,immediate after fifteen session,Three months after the end of treatment. Method of measurement: visual analogous scale.

Secondary

MeasureTime frame
Disability. Timepoint: pre treatment, immediate after fifteen sessions , Three months after the end of treatment. Method of measurement: Oswestry disability index.;Fear of movement. Timepoint: pre treatment, immediate after fifteen sessions , Three months after the end of treatment. Method of measurement: tampa scale.;Thickness of transverse abdominis muscle. Timepoint: pre treatment, immediate after fifteen sessions , Three months after the end of treatment. Method of measurement: sonography.;Brain wave. Timepoint: pre treatment, immediate after fifteen sessions , Three months after the end of treatment. Method of measurement: neurofeedback.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGolnaz Sadria

University of social welfare and rehabilitation sciences

gl.sdr9019@gmail.com+98 21 2218 0083

Outcome results

None listed

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