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The effect of self-management program on elderly patients with non-specific chronic low back pai

Not Applicable
Recruiting
Conditions
Chronic Low Back Pain.
Low Back Pain
M54.5
Registration Number
IRCT20110912007529N25
Lead Sponsor
Shahed University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
64
Inclusion Criteria

Willingness to participate in the study
60 years of age or older
Married
Having Lower back pain for more than three months without any pathological cause
No cognitive impairment based on the Abbreviated Mental Test (AMT)
Have not difficult Known mental illness based on the contents of the health record
Live in the city of Abadan and related countryside areas
Not participating in similar interventions
Capable of exercise according to a physician’s opinion
No drug and alcohol addiction
Subjects should not have any history of other illnesses (such as infection, Inflammatory diseases, Autoimmune and malignant diseases, Osteoporosis, Fracture, and Herniation disk), Congenital anomalies (With the exception of mild lordosis and scoliosis), Surgical interventions, Injury to the knee and ankle that restricts movement.

Exclusion Criteria

Not participating in the study
Do not attend or miss more than one session in the training program
Patients who have a change in therapeutic intervention during the study according to the physician’s opinion
Low back injury during the study

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The intensity of pain. Timepoint: The intensity of pain will be evaluated before intervention, 4 weeks after intervention, and 8 weeks after intervention. Method of measurement: Visual Pain Scale.;Disability. Timepoint: The Disability will be evaluated before intervention, 4 weeks after intervention, and 8 weeks after intervention. Method of measurement: Oswestry Disability Questionnaire (ODQ).
Secondary Outcome Measures
NameTimeMethod
Quality of Life. Timepoint: The Quality of Life will be evaluated before intervention, 4 weeks after intervention, and 8 weeks after intervention. Method of measurement: ???????? ??????? ???????(ODQ).
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