To address the primary objective, arterial stiffness in the experimental group will be analyzed and compared with the control group and the physical activity orientation group. To address the secondary objectives, various variables related to quality of life, cognitive functions, and disease activity will be compared between different patient groups. The levels of inflammation and immunosenescence and the relationship between these two dimensions will be analyzed before and after the exercise program in the experimental group of RA and CKD patients, with patients serving as their own controls.
The first contact with CKD patients will be in the Nephrology Department, and for RA patients, in the Rheumatology Department during their regular medical visits. Initially, investigators will screen potential patients for participation. The screening process involves a thorough evaluation of medical characteristics, health history, and other pre-established criteria to identify subjects who meet the specific inclusion criteria of this study.
The evaluations described in the initial assessment will be conducted, and all enrolled subjects will undergo a resting ECG, with the investigator recording data for each subject. Patient treatments will not be interrupted during the entire protocol period. All patients will be evaluated twice: once during the inclusion visit and again after 6 weeks.
During the inclusion visit, the patient will complete questionnaires, then rest in a lying position for 10 minutes. An initial evaluation lasting about 10 minutes will be conducted in a lying position, including measurements of blood pressure, heart rate, reactive hyperemia (to evaluate endothelial function), and pulse wave velocity (PWV). The total duration will be 25 minutes. After then, for control group patients and physical activity orientation group patients, the session ends here.
For experimental group patients, the patient will then perform physical activity on a cycle ergometer for 47 minutes. The same assessments will be conducted at the end of the session For invasive measures, venous blood samples will be taken from the elbow crease by a clinical research nurse. A total of 2 dry tubes of 5 ml and 2 EDTA purple tubes of 5 ml will be collected at the beginning and end of the rehabilitation protocol (6 weeks), totaling 40 ml. For experimental groups, an additional blood sample will be taken during follow-up, 6 weeks after the end of the rehabilitation program, totaling 60 ml for these groups.
Endothelial function will be assessed by measuring pulse wave velocity and reactive hyperemia. Arterial compliance (central and peripheral) will be assessed by measuring the pulse wave velocity on the carotid-femoral and carotid-radial segments, respectively, using the Complior (Complior SP®, Artech Medical, Pantin, France). Reactive hyperemia will be assessed with ENDOPAT (Itamar Medical®, Caesarea, Israel), which quantifies peripheral vasodilatory response non-invasively via electronic finger cuffs following blood flow occlusion.
Hemodynamic parameters will be evaluated by measuring heart rate and blood pressure with the Finapres during assessments. Heart rate monitoring during cycling in experimental groups will use the Polar A300 heart rate monitor. Blood pressure will be measured before and after exercise with the Omron.
The interventions during the 6 weeks for the experimental group - exercise sessions will be conducted in the nephrology or rheumatology departments, supervised by an adapted physical activity professional, scheduled for three weekly 47-minute sessions over 6 weeks (18 sessions). Exercise intensity will be adjusted based on individual heart rate reserve, starting at 40% and progressing to 70% by the final session. Each session includes a warm-up, main exercise phase, and active recovery.
The interventions during the 6 weeks for the PA orientation group - Every week, for around ten minutes, patients in the PA orientation group will be contacted by telephone. The main objective of this exchange is to provide targeted advice on physical activity, its role, its objectives as well as its different ways of carrying it out. The second objective is to provide each week a personalized objective for each patient which can evolve over the weeks in order to increase levels of physical activity as far as possible. Call Procedure are: establishing a diagnosis carried out using questionnaires distributed beforehand (level of physical activity, quality of life); contribution of advice and explanation around physical activity: The evaluator (adapted physical activity teacher) will provide knowledge about PA, its roles and objectives, recommendations, and different ways of practice; lifestyle exchange (personalized): An exchange between the professional and the patient to understand the patient's lifestyle habits; setting a therapeutic objective: Propose an objective around physical activity based on the patient's needs and lifestyle and answer patient questions: Reflective listening and open-ended questions will facilitate the exchange.
