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Effectiveness of group exercise therapy with the instructional pack in improvement of patients with low back pain

Effectiveness of group exercise therapy with the instructional pack versus usual physiotherapy programme in improvement of patients with low back pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015041921847N1
Enrollment
70
Registered
2015-08-31
Start date
2015-05-22
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

chronic low back pain.

Interventions

Intervention 1: "The intervention group": The intervention group members will receive Usual physiotherapy treatment plus group exercise therapy classes which are held by the physiotherapist twice a
Rehabilitation
"The intervention group": The intervention group members will receive Usual physiotherapy treatment plus group exercise therapy classes which are held by the physiotherapist twice a week. the walki
" Control group: the group which receive usual physiotherapy treatment includes TENS, Ultrasound, Hot pack, Laser and exercise for 6 weeks"

Sponsors

Vice chancellor for research,Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients with mechanical chronic low back pain above 3 months? Male and female age between 18 to 65? Patients without spinsl surgery during last year Exclusion criteria: Duration of low back pain under 3 months? History of inflammatory systemic diseases such az Rheumatoid arthritis? History of severe spinal canal stenosis such as Spondylolisthesis and Fibromyalgia? History of cancers or recent radiotherapy and chemotherapy? Pregnancy? Cardiovascular disease? Severe psichiatric diseases? Surgery of spinal cord? Lumbar physiotherapy during recent 6 months? Illiterate patients

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Befor treatment and after first and second month of treatment. Method of measurement: Visual analog score.;Functional disability. Timepoint: Befor treatment and after first and second month of treatment. Method of measurement: Oswestry Disability Index Questionnaire.;Respiratory function. Timepoint: Befor treatment and after first and second month of treatment. Method of measurement: spirometry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArmin Sahba

Semnan University of Medical Sciences

arminsahba@yahoo.com+98 23 3332 2332

Outcome results

None listed

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