Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 12:14 AM
Ignite Modification Date: 2025-12-25 @ 12:14 AM
NCT ID: NCT04331158
Eligibility Criteria: Inclusion Criteria: * Diagnosed with KOA based on ACR clinical criteria; * Knee pain intensity between 3 and 8, according to the Numerical Pain Scale (END); * BMI less than 35 kg / m2. Exclusion Criteria: * Having undergone physical therapy treatment for the knee in the 3 months prior to the project; * Be engaged in\> 45 minutes / week in accumulated physical activity of at least moderate intensity; * To have been submitted to the application and / or intervention with the wind therapy previously. * Have used corticosteroid infiltration in the knee in the last 6 months; * Present any medical restrictions that make it impossible for them to participate in the proposed assessments and interventions (cardiorespiratory, neurological and / or musculoskeletal changes); * Presenting a diagnosis of fibromyalgia, rheumatoid arthritis or some systemic inflammatory arthritis; * Presenting a ligament or meniscal injury diagnosed clinically or with a positive result in the Apley tests or anterior / posterior drawer; * Have had previous surgery on the ankle, knee or hip; * Present a clinical diagnosis of some dementia or inability to answer the questionnaires related to the study; * Present any contraindications for the use of ventosatherapia (skin lesion in the region where it will be applied, cancer, kidney failure, liver and heart failure, pacemaker, pregnancy); * Having uncontrolled diabetes and hypertension; * Have a trip scheduled for the two months following inclusion in the survey.
Healthy Volunteers: False
Sex: FEMALE
Minimum Age: 50 Years
Maximum Age: 75 Years
Study: NCT04331158
Study Brief:
Protocol Section: NCT04331158