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

The efficacy self-management program based on 5A model self in improving pain, functional disability, and quality of life among older people with non-specific chronic low back pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110912007529N25
Enrollment
64
Registered
2022-12-03
Start date
2023-01-21
Completion date
Unknown
Last updated
2023-02-07

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

Conditions

Chronic Low Back Pain. Low Back Pain

Interventions

Intervention 1: Intervention group: Educational sessions will be held in elderly people with low back pain in 5 steps over 6 weeks and each session will be 45-60 minutes. Based on the training, the A-

Sponsors

Shahed University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Nahid Rejeh

Shahed University

nrejeh@yahoo.com+98 21 5121 2150

Outcome results

None listed

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