Knee osteoarthritis. Unilateral primary osteoarthritis of knee
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Diagnosis of knee osteoarthritis by physicians (mild, moderate) Age 50 and older BMI 41-27 Has the cognitive ability to complete the learned forms of food The desire to participate in the study
Exclusion criteria
Exclusion criteria: Get daily calories less than 800 and more than 4200 kcal Follow a special food pattern for medical reasons or other reasons Infection with other inflammatory diseases, such as rheumatoid arthritis Diabetes Other musculoskeletal problems, including back pain Having a history of radiotherapy Intra-articular intra-articular injection 3 months ago Oral use (nonsteroidal anti-inflammatory drugs) from a week before entering the study Depression (gaining a score of more than 5 from the Geriatric Depression Scale, GDS-15) History of neurological diseases or drug use People who for any reason are not able to cooperate in completing questionnaires and plans Use of dietary supplements, diuretics or laxatives during the intervention period Participate in sports programs or change physical activity Performing physiotherapy in the last 3 months Use of nonsteroidal anti-inflammatory drugs during the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Functional status and pain associated with osteoarthritis in the lower extremities. Timepoint: Before and after the intervention. Method of measurement: Western Ontario and McMaster (WOMAC).;BMI. Timepoint: The beginning and the end of the study. Method of measurement: The result of dividing the weight into kilograms by squared height in meters.;Waist. Timepoint: The beginning and the end of the study. Method of measurement: Strip meter.;Hip circumference. Timepoint: The beginning and the end of the study. Method of measurement: Strip meter.;Severity of anxiety. Timepoint: The beginning and the end of the study. Method of measurement: Two-part questionnaire of Spielberger's apparent and hidden anxiety.;Depression rate. Timepoint: The beginning and the end of the study. Method of measurement: Beck Depression Inventory.;The amount of pain. Timepoint: The beginning and the end of the study. Method of measurement: VAS (Visual Analogue Scale).;Quality of Life. Timepoint: The beginning and the end of the study. Method of measurement: SF-36 quality of life questionnaire.;Biochemical analysis of blood samples. Timepoint: The beginning and the end of the study. Method of measurement: Biochemical analysis of blood samples. | — |
Countries
Iran (Islamic Republic of)
Contacts
Tabriz University of Medical Sciences