The Effect of Home-based Rehabilitation on the Treatment of Knee Qsteoarthritis

The Effect of Home-based Rehabilitation Ttraining on Pain, Performance, General Health and Quality of Life in Patients with Knee Osteoarthritis

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2017100218117N2

Enrollment

Registered

2017-11-19

Start date

2017-10-23

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. [Gonarthrosis [arthrosis of knee

Interventions

Intervention 1: "Intervention group: Implementation of three 1-hour sessions "Individual training and practice in the following order: The first training session on knee osteoarthritis, the causes of

Rehabilitation

"Intervention group: Implementation of three 1-hour sessions "Individual training and practice in the following order: The first training session on knee osteoarthritis, the causes of symptoms, sympt

"The control group: does not receive rehabilitation training and receive routine therapies."

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Inclusion criteria: No history of surgical related disease (such as joint replacement, joint repair), having radiological symptoms of osteoarthritis in knee with a physician's approval, non-use of an intra-articular injectable drug, the absence of any mental and psychological illness according to the patient's own statements, and independence in self-care. Exclusion criteria: The first referral of the patient and the lack of diagnosis by the doctor, the lack of regular referral of the patient, the patient's reluctance to continue treatment, and exacerbation of symptoms.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: Before the intervention, two months after the intervention. Method of measurement: Visual Scale of Pain.;Performance. Timepoint: Before the intervention, two months after the intervention. Method of measurement: Scale KOOS.;General health. Timepoint: Before the intervention, two months after the intervention. Method of measurement: General Health Questionnaire.;Quality of Life. Timepoint: Before the intervention, two months after the intervention. Method of measurement: Quality of Life Questionnaire (SF-36).	—

Measure

Time frame

Pain. Timepoint: Before the intervention, two months after the intervention. Method of measurement: Visual Scale of Pain.;Performance. Timepoint: Before the intervention, two months after the intervention. Method of measurement: Scale KOOS.;General health. Timepoint: Before the intervention, two months after the intervention. Method of measurement: General Health Questionnaire.;Quality of Life. Timepoint: Before the intervention, two months after the intervention. Method of measurement: Quality of Life Questionnaire (SF-36).

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Hosseinabadi

Bushehr University of Medical Sciences

Hosseinabadz374@gmail.com+98 77 3345 0084

Outcome results

None listed

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