Chronic Renal Failure Clinical Trial
Official title:
Physical Activity in Dialysis: Clinical and Biological Impact
NCT number | NCT04525196 |
Other study ID # | Dialyse |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | January 29, 2021 |
Est. completion date | July 29, 2025 |
Physical inactivity is known to increase the risk of developing many diseases as cardiovascular diseases, diabetes, some cancers, and other chronic diseases. The impact of the inactivity is even higher in a fragile population as patients with Chronic Renal Failure (CRF) who need dialysis. This can lead to serious adverse events during the lifetime of these patients, such as arteriopathy which can result in amputation, deterioration of general condition, loss of independence and depression of wasting away. Despite the need to promote physical activity in this population of hemodialysis patients with CRF, little is known about the effects of a supervised physical activity conducted in these patients. With this study, the investigators propose to assess the effects of a physical activity program on several parameters, in hemodialysis subjects.
Status | Recruiting |
Enrollment | 250 |
Est. completion date | July 29, 2025 |
Est. primary completion date | July 29, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Male or female aged 18 or over. - Patient on hemodialysis. - Patient in sufficient clinical condition allowing performing physical activity sessions during dialysis, according to the judgment of the investigator. - Patient who was informed of the study and who gave his informed consent. - Patient benefiting from a mandatory social security. Exclusion Criteria: - Recent myocardial infarction (<1 month). - Rheumatological pathology which does not allow pedaling. - Unmatched amputation of the lower limbs. - Patients under legal protection. - Pregnant or breastfeeding women. |
Country | Name | City | State |
---|---|---|---|
France | Clinique Bouchard | Marseille | |
France | Polyclinique les Fleurs | Ollioules |
Lead Sponsor | Collaborator |
---|---|
Elsan |
France,
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* Note: There are 15 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The clinical impact of a physical activity program on the walking capacity. | Measure and evolution of the performance to the 6 minutes walking test. | Baseline. | |
Primary | The clinical impact of a physical activity program on the walking capacity. | Measure and evolution of the performance to the 6 minutes walking test. | 6 months after the inclusion. | |
Secondary | The clinical impact of a 12 month physical activity program on the aeroby capacity of the patients. | Measure and evolution of the performance to the 6 minutes walking test. | At the randomization visit, and 12 months after the inclusion. | |
Secondary | The clinical impact of a physical activity program on the muscle binding. | Measure and evolution of the extension force of the lower limbs. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | The clinical impact of a physical activity program on the muscle binding. | Measure and evolution of the extension force of the handgrip. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | The clinical impact of a physical activity program on the muscle binding. | Measure and evolution of the extension force of the elbow flexion. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | The clinical impact of a physical activity program on the muscle binding. | Measure and evolution of the extension force of the sit/stand up test. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | The impact of a physical activity program on the nutritional status. | Measure and evolution of the weight in kg. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | The impact of a physical activity program on the nutritional status. | Measure and evolution of the BMI in kg/m². | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | The impact of a physical activity program on the nutritional status. | Measure and evolution of the body surface given in m². | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | The impact of a physical activity program on the nutritional status. | Measure and evolution of the active cell mass in kg. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | The impact of a physical activity program on the nutritional status. | Measure and evolution of the muscle mass in kg. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | The impact of a physical activity program on the nutritional status. | Measure and evolution of the mass index lean in kg. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | The impact of a physical activity program on the nutritional status. | Measure and evolution of the albuminemia in g/L. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | The impact of a physical activity program on the nutritional status. | Measure and evolution of the pre-albuminemia in g/L. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | The impact of a physical activity program on the nutritional status. | Measure and evolution of the nPCR (Normalized Protein Catabolic Rate) in g/kg/day. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | The impact of a physical activity program on the nutritional status. | Measure and evolution of the creatinine in mmol/L. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | The impact of a physical activity program on the Obstructive Arterial Disease of the Lower Limbs. | Measure and evolution of the systolic pressure index and the systolic pressure of the toe measured by the SYSTOE, the number of revasularisations, the number of ischemic wounds, the number of amputations, and the number of deaths linked to the Obstructive Arterial Disease of the Lower Limbs. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | To assess the impact on a physical activity program on the biological parameters. | Measure and evolution of the hemoglobin in g/dl. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | The impact on a physical activity program on the biological parameters. | Measure and evolution of the CRP in µg/mL. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | The impact on a physical activity program on the biological parameters. | Measure and evolution of the PTH in pg/mL. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | To assess the impact of a physical activity program on the quality of life. | Evolution of the score obtained at the SF-36 questionnaire. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | The impact of a physical activity program on the survival. | Evolution of the vital status. | At the randomization visit, 6 months after the inclusion and 12 months after the inclusion. | |
Secondary | To assess the impact of a physical activity program on the the relationship between caregivers and patients, the creation of social ties and "coping" (the ability to cope and adapt in response to stress) | Evolution of the score obtained at the WCC-R questionnaire. | At the randomization visit, and 6 months after the inclusion. | |
Secondary | The compliance with physical activity. | Development of aerobic capacity: the duration and, if applicable, the resistance level will be specified for each session. | After each physical activity session performed by the patient. | |
Secondary | The compliance with physical activity. | Muscle strengthening: the number of repetitions performed and the resistance level will be specified for each session. | After each physical activity session performed by the patient. | |
Secondary | The tolerance to physical activity. | Adverse events: collection of the frequency and severity. Collection of the adverse events related to the PA program (group experimental only). | 1 year, during each physical activity session. |
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