Actively Recruiting
Beetroot Extract Supplementation Associated With an Exercise Protocol for Chronic Kidney Disease Patients
Led by Universidade Federal Fluminense · Updated on 2025-04-04
25
Participants Needed
1
Research Sites
139 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Chronic kidney disease (CKD) patients often present systemic inflammation and oxidative stress, resulting in metabolic disorders and high rates of disease-associated cardiovascular death. The literature has indicated that dietary control, the use of bioactive compounds, and the practice of regular physical exercise are essential for the prevention and management of CKD and its complications. In this context, beetroot (Beta vulgaris rubra) deserves attention as it is a source of several bioactive compounds, such as nitrate, betaine, and betalain, with beneficial effects for CKD patients, including anti-inflammatory, antioxidant effects, reduction of blood pressure, and vasodilatory action. The antioxidant and anti-inflammatory properties, in addition to their vasodilatory and antihypertensive capacity, can make supplementation of beetroot an excellent nutritional strategy to help in the treatment of CKD patients. So, this research project will bring contributions to the scientific world, providing strategies for application in clinical practice and the care of patients with CKD, on the use of beetroot associated with an exercise protocol as a non-pharmacological strategy in modulating inflammation, oxidative stress, and improved functional capacity. Furthermore, when supplemented hours before physical training, has been identified as an important factor in improving performance in these activities. Therefore, this study aims to evaluate the effects of supplementation (acute and chronic) of beetroot extract associated with an exercise protocol on complications associated with CKD.
CONDITIONS
Official Title
Beetroot Extract Supplementation Associated With an Exercise Protocol for Chronic Kidney Disease Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with CKD undergoing conservative treatment (stages G3a-G4)
- Aged between 18 and 65 years old
- Patients undergoing nutritional monitoring for more than 6 months
You will not qualify if you...
- Patients using catabolic drugs
- Smokers
- Pregnant women
- Using antibiotics or proton pump inhibitors in the last 3 months
- Taking antioxidant supplements or regularly consuming beetroot or nitrate supplements
- Clinically unstable patients (unstable angina, atrial fibrillation, significant arrhythmia, recent acute illness, glycemic instability)
- Unable to exercise due to amputation without prosthesis, musculoskeletal pain, inability to sit or walk without help, use of walking device, or dyspnea at rest or with light exertion
- Having autoimmune diseases, infectious diseases, cancer, liver disease, or AIDS
- Patients with parathormone (PTH) levels above 500 pg/mL
- Allergic or intolerant to juice components
- Unable to complete exercise protocol due to travel or access difficulties
AI-Screening
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Trial Site Locations
Total: 1 location
1
Denise Mafra
Rio de Janeiro, Rio de Janeiro, Brazil, 22260050
Actively Recruiting
Research Team
D
Denise Mafra, PhD
CONTACT
D
Denise Mafra, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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