Tailored internet–based treatment of low back pain

The effect of tailored internet–based intervention in patient with non specific persistent low back pain

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2012121211736N1

Enrollment

Registered

2012-12-27

Start date

2012-12-20

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Diseases of the musculoskeletal system andconnective tissue. Low back pain Loin pain Low back strain Lumbago NOS

Interventions

Intervention 1: Intervention group subjects were educated weekly information about low back pain and asked to perform tailored exercises (strengthening, and stretching and core stability) weekly shown

Rehabilitation

Intervention group subjects were educated weekly information about low back pain and asked to perform tailored exercises (strengthening, and stretching and core stability) weekly shown on the LBP spec

The subjects in control group received some untailored exercise (strengthening, and stretching and core stability) and information in one time after allocating to study

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:18 – 65 years old. non-specific low back pain (more than 6 weeks). Internet access and have an e-mail. Able to read and write Farsi. Exclusion criteria: excessive weight loss in recent months.cancer. malaise.fever.urin and bowl incontinency. needles sensation and numbness in the lower knee. a history of recent trauma to the low back. The decision to perform surgery on the lumbar spine. use a wheelchair. having another disability in addition to back pain.pregnancy .night pain. use of oral corticosteroids.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain intensity. Timepoint: at baseline and at 12 weeks later. Method of measurement: visual analog scale (VAS 0-10 cm).	—

Secondary

Measure	Time frame
Disability. Timepoint: at baseline and at 12 weeks later. Method of measurement: Roland morris disability questionnaire.;Quality of life. Timepoint: at baseline and at 12 weeks later. Method of measurement: (WHOQOL) –BREF questionnaire for quality of life.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Ramin Kordi

Sport Medicine Research Center, Tehran University of Medical Sciences and Health Services

ramin_kordi@sina.tums.ac.ir+98 21 8863 0227

Outcome results

None listed

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