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The effect of tele-rehabilitation nursing on knee osteoarthritis

Not Applicable
Recruiting
Conditions
Knee osteoarthritis.
Osteoarthritis of knee
Registration Number
IRCT20220216054038N1
Lead Sponsor
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Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
36
Inclusion Criteria

Complete and sign the consent form
Being 18-60 years old
Having chronic knee pain for the past three months
Having primary type of knee osteoarthritis
Based on the 0-4 Kellgren and Lawrence scale, people with a severity of 1-3 osteoarthritis of the knee according to this criterion
No history of disease-related surgery (such as replacement and joint repair)
Absence of any other disease around the affected limb
Do not give any intra-articular injections during the last three months
Having a smartphone and internet access
Ability to use a smartphone
Failure to participate in similar research

Exclusion Criteria

People who are being treated with physiotherapy, chiropractic or acupuncture
Secondary knee osteoarthritis such as secondary to gout, metabolic arthritis, inflammatory rheumatism
Grade 0 and 4 Kellgren-Lawrence scale recorded in the client's medical record and approved by the treating physician
Morning joint stiffness more than 30 minutes
History of trauma, fracture and dislocation of the affected knee
Having radiculopathy or nerve damage and neuropathies
Severe cognitive or mental disorder (dementia, Alzheimer's ...) that is recorded in the client's medical record and approved by the treating physician.
History of allergies to herbal supplements and dietary recommendations used in the study
Pregnant women or women who decide to become pregnant
Use of anticoagulants
Diseases or other malignancies (such as unstable cardiovascular disorders or lung disease, cancer, dementia) that limit the ability to adhere to recommended OA treatment, or uncontrolled diabetes
Chronic use of Narcotics
Inability to communicate and complete questionnaires
Patients' unwillingness to continue participating in the training course

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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