Knee Arthrosis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Aged 60 years or older; engage in a minimum of 45 minutes per week of accumulated physical activity at a moderate intensity level; report a pain intensity equal to or exceeding 4 cm on a 10-cm visual analogue scale
Exclusion criteria
Exclusion criteria: Individuals who had undergone physiotherapy in the previous 3 months; received knee injections in the previous 6 months; had medical constraints, such as cardiorespiratory, neurological, or rheumatological dysfunctions; had undergone prior hip, knee, or ankle surgery; had chronic conditions leading to knee pain
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1: It is expected to find a reduction of at least 30% in pain, verified through the Numeric Verbal Scale (NVS) method, between the pre and post-intervention periods.;Outcome found 1: A reduction of 30% or more in pain was observed in all groups, verified through the Numeric Verbal Scale (NVS) method, between the pre and post-intervention periods. | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome 3: no significant difference in range of motion is expected, as assessed by the painful and total range of motion test, between the pre and post-intervention periods.;Outcome found 3: no significant difference in range of motion was found, as assessed by the range of motion test, between the pre and post-intervention periods.;Expected outcome 2: no differences in temperature are expected, as verified through the thermography method, between the pre and post-intervention periods.;Outcome found 2: no differences in temperature were found, as verified through the thermography method, between the pre and post-intervention periods. | — |
Countries
Brazil
Contacts
Faculdade de Ceilândia da Universidade de Brasília