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Therapeutic exercise in knee osteoarthritis

Comparison of the short-term effects of clinically supervised and Internet-based exercise therapy on pain, range of motion, and function in patients with knee osteoarthritis: a randomized clinical trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20101228005486N8
Enrollment
60
Registered
2021-03-17
Start date
2021-05-15
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

Primary knee osteoarthritis. Osteoarthritis of knee

Interventions

Intervention 1: Intervention group: Internet-based Exercise Therapy(IET) group-First, Internet connectivity and instant message systems will be examined for patients in the Internet-based exercise the

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
50 Years to 75 Years

Inclusion criteria

Inclusion criteria: Primary OA of the knee joint grade 2, 3 according Kellgren and Lawrence scale; ?Female gender; Age between 50-75; Knee pain for at least six months and with intensity 4 on the VAS scale in activities such as going up and down stairs, sitting and squat; Normal mental state; Ability to walk independently for at least 30 meters BMI equal or less than 30; Patient's consent to participate in the research; Familiarity how to use the Internet and social media for the Internet-based Exercise Therapy (IET) group.

Exclusion criteria

Exclusion criteria: History of knee intra-articular injection in the past six months; History of neuromuscular disease; History of knee traumatic injuries approved by the physician; History of lower limb surgery during the last year; Bone implants, History of new fractures in lower limbs; Malignant tumors; Participating in exercise therapy and physical therapy programs in the recent three months; History of chronic disease or any conditions that known to affect the study;

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Pre- and post-intervention. Method of measurement: VAS pain scale.;Active knee range of flexion. Timepoint: Pre- and post-intervention. Method of measurement: Goniometery.;Thigh girth. Timepoint: Pre- and post-intervention. Method of measurement: With centimeter tape.

Secondary

MeasureTime frame
Functional Tests. Timepoint: Pre- and post-intervention. Method of measurement: Timed Up & Go Test and Six-Minute Walk Test.

Countries

Iran (Islamic Republic of)

Contacts

Public Contact?Dr Bita Zoghalchi

Iran University of Medical Sciences

bita.zoghalchi@gmail.com+98 21 6435 2446

Outcome results

None listed

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