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Comparison of the effect of online and face-to-face cognitive exercises in people with non-specific chronic low back pain

Comparison of the effect of online and face-to-face cognitive exercises in people with non-specific chronic low back pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150503022068N4
Enrollment
66
Registered
2021-08-25
Start date
2021-06-02
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Non specific low back pain. Low back pain

Interventions

Intervention 1: Intervention group: 3 online sessions of pain neuroscience education, followed by 15 online sessions of education and exercises of motor control _cognition. The intervention will be d

Sponsors

Kharazmi University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 55 Years

Inclusion criteria

Inclusion criteria: At least time for low back pain is 12 weeks and 3 days a week. Pain should be determined at the discretion of a physician and also using the Quebec questionnaire. People are in the medium risk group according to the Start Back tool Score 14% or more on the Oswestry Disability Index Has a pain intensity equal to or greater than 4 on a numerical rating scale The pain is between the last rib and the gluteal Have not taken any new medication or people who do not need medication during the 6 weeks before and while studying Body mass index less than or equal to 30 Women and men 25 to 55 years

Exclusion criteria

Exclusion criteria: Pregnant women People with a history of lumbar tumors People with inflammatory disease of the spine that is mentioned in their medical history or has been diagnosed by a doctor Participate in exercise therapy courses for the treatment of low back pain in the past year Having any fractures and surgery in the lumbar and dorsal spine

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before and after the intervention. Method of measurement: Numerical pain rating scale.;Disability. Timepoint: Before and after the intervention. Method of measurement: Oswestry Disability Index.

Secondary

MeasureTime frame
Function. Timepoint: Before and after the intervention. Method of measurement: McGill tests and Luomajoki motor control tests.;Psychological factors. Timepoint: Before and after the intervention. Method of measurement: Tampa scale- Dass21 questioner- Fear Avoidance Belief Questionnaire- Self-Efficacy Questionnaire- Pain Catastrophizing Scale.;Health status. Timepoint: Before and after the intervention. Method of measurement: Asking questions.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGelareh Alamouti

Kharazmy University

gelarehalamooti@gmail.com+98 21 2222 8001

Outcome results

None listed

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