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Comparison of the effects of routine physiotherapy and Pilates exercise on pain, function and quality of life in women with knee osteoarthritis

Comparison of the effects of routine physiotherapy and Pilates exercise on pain, function and quality of life in women with knee osteoarthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201604041552N6
Enrollment
20
Registered
2016-07-02
Start date
2016-06-21
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

Osteoarthritis of knee. Gonarthrosis [arthrosis of knee]

Interventions

Intervention 1: Control group treated with 12 ( 4 weeks ,3 sessions ) sessions of low-frequency TENS & hot pack for 20 minutes, continuous ultrasound treatment for 5 minutes and exercise. Intervention
Rehabilitation
Control group treated with 12 ( 4 weeks ,3 sessions ) sessions of low-frequency TENS & hot pack for 20 minutes, continuous ultrasound treatment for 5 minutes and exercise
Intervention group over 12 sessions ( 4 weeks ,3 sessions ) treated with Pilates exercises

Sponsors

Vice- Chancellor for Research Affirs of Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
50 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: women with knee osteoarthritis , age range 50_70 years old; have a pain in the range of 30_70 mm based on the VAS, score 2 or 3 of standard Modified Altman. Exclusion criteria: have been experienced physiotherapy or exercise therapy in the past 6 months; history of joint tap or steroid injection in the last year; active inflammation of the knee; pain at the hip and ankle; history of fracture or dislocation of lower limbs; any deformities in the lower extremitiesl; osteoporosis based on the criteria of T-Score (T= -2.5); history of systemic, immune system, cardiovascular diseases.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before and after treatment sessions. Method of measurement: Visual analog scale.

Secondary

MeasureTime frame
Function. Timepoint: Before and after treatment sessions. Method of measurement: timed up and go test and 30 second chair stand test.;Quality of life. Timepoint: Before and after treatment sessions. Method of measurement: SF39 questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahsa Zahedi

Rehabilitation Sciences School of Shiraz University of Medical Sciences

mhs.zahedi72@gmail.com+98 71 3627 1551

Outcome results

None listed

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