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prayer knee brace

Designing, manufacturing and evaluating the effectiveness of prayer knee brace in patients with mild knee osteoarthritis pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180619040148N2
Enrollment
10
Registered
2019-05-01
Start date
2019-06-20
Completion date
Unknown
Last updated
2019-05-21

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

Conditions

patients with mild knee osteoarthritis pain. Osteoarthritis of knee

Interventions

Intervention group: prayed knee brace. Light and thin knee brace that do not prevent knee bending. The anterior side of the knee brace is made of foam, which reduces knee forces when kneeling..

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Knee osteoarthritis Grade 3 and 4 (Kellgren-lawrence Grade) According to the orthopedic surgeon Age between 30 - 60 years Mild knee pain based on Visual Analog Scale

Exclusion criteria

Exclusion criteria: History of surgery associated with the disease (such as replacement and joint repair) History of knee fracture Chronic illness such as insulin-dependent diabetes or lupus Corticosteroid injections into the knee joint during the 30 days prior to the intervention or the injection program until the end of the study period

Design outcomes

Primary

MeasureTime frame
Pain rate when kneeling based on WOMAC questionnaire. Timepoint: Before intervention and 30 days after knee brace use. Method of measurement: WOMAC questionnaire (Western Ontario and McMaster osteoarthritis index).;Joint stiffness. Timepoint: Before intervention and 30 days after knee brace use. Method of measurement: WOMAC questionnaire (Western Ontario and McMaster osteoarthritis index).;Functional activity. Timepoint: Before intervention and 30 days after knee brace use. Method of measurement: WOMAC questionnaire (Western Ontario and McMaster osteoarthritis index).;Range of motion. Timepoint: Before intervention and 30 days after knee brace use. Method of measurement: Digital goniometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasumeh Bagherzadeh Cham

Iran University of Medical Sciences

BagherzadehCham.m@iums.ac.ir+98 21 8214 1612

Outcome results

None listed

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